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Xanthones from Fungi, Lichens, and Bacteria: The Natural Products and Their Synthesis
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Invasive Methicillin-Resistant Staphylococcus aureus Infections in the United States
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Natural and Synthetic Xanthones as Monoamine Oxidase Inhibitors: Biological Assay and 3D-QSAR
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Secalonsäure, ein 8.8′‐Dichromonyl aus Mutterkorn Mutterkorn‐Farbstoffe, III
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Struktur der Secalonsäuren A und B [1]
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A Short, Atom‐Economical Entry to Tetrahydroxanthenones
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The Total Synthesis of the Fungal Metabolite Diversonol
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First Stereoselective Total Synthesis of FD‐594 Aglycon
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inferredcites →https://doi.org/10.1002/cber.19320650850openalex-snapshot
Über die gelben Farbstoffe des Mutterkorns, I. Mitteil.: Das Ergoflavin
inferredcites →https://doi.org/10.1002/cber.19320650851openalex-snapshot
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inferredcites →https://doi.org/10.1002/cber.19620950604openalex-snapshot
Mutterkorn‐Farbstoffe, IV. Zur Konstitution der Secalonsäure
inferredcites →https://doi.org/10.1002/cber.19630961216openalex-snapshot
Mutterkorn‐Farbstoffe, V. Synthese und Wessely‐Moser‐Umlagerung von 8.8′‐und 6.6′‐Bichromonylen
inferredcites →https://doi.org/10.1002/cber.19660991218openalex-snapshot
Mutterkorn‐Farbstoffe, XII. Trennung, Struktur und absolute Konfiguration der diastereomeren Secalonsäuren A, B und C
inferredcites →https://doi.org/10.1002/cber.19660991219openalex-snapshot
Mutterkorn‐Farbstoffe, XIII. Isolierung, Struktur und absolute Konfiguration der Ergochrysine A und B
inferredcites →https://doi.org/10.1002/cber.19660991220openalex-snapshot
Mutterkorn‐Farbstoffe, XIV. Isolierung, Struktur und absolute Konfiguration der Ergochrome AD, BD, CD und DD
inferredcites →https://doi.org/10.1002/cber.19681010610openalex-snapshot
Mutterkorn‐Farbstoffe, XVII. Biosynthese der Ergochrome
inferredcites →https://doi.org/10.1002/cber.19681010611openalex-snapshot
Mutterkorn‐Farbstoffe, XVIII. Emodin als Biosynthesevorstufe der Ergochrome
inferredcites →https://doi.org/10.1002/cber.19731060417openalex-snapshot
Pilzinhaltsstoffe, 23. Stereospezifische Synthese der 10‐Methyl‐10‐desmethoxycarbonyl‐hemisecalonsäure A
inferredcites →https://doi.org/10.1002/chem.200501485openalex-snapshot
Diastereoselective Synthesis of Highly Functionalized Tetrahydroxanthenols—Unprecedented Access to Privileged Structural Motifs
inferredcites →https://doi.org/10.1002/chem.200601236openalex-snapshot
Kibdelones: Novel Anticancer Polyketides from a Rare Australian Actinomycete
inferredcites →https://doi.org/10.1002/chem.200800035openalex-snapshot
New Mono‐ and Dimeric Members of the Secalonic Acid Family: Blennolides A–G Isolated from the Fungus Blennoria sp.
inferredcites →https://doi.org/10.1002/chem.200800967openalex-snapshot
Stereoselective Synthesis of 4‐Dehydroxydiversonol Employing Enantioselective Palladium‐Catalysed Domino Reactions
inferredcites →https://doi.org/10.1002/chem.200801507openalex-snapshot
Modular Syntheses of Diversonol‐Type Tetrahydroxanthone Mycotoxins: Blennolide C (epi‐Hemirugulotrosin A) and Analogues
inferredcites →https://doi.org/10.1002/chem.200900749openalex-snapshot
Xanthones and Oxepino[2, 3‐b]chromones from Three Endophytic Fungi
inferredcites →https://doi.org/10.1002/chem.201102192openalex-snapshot
A Unified Strategy for the Asymmetric Total Syntheses of Diversonol and Lachnone C
inferredcites →https://doi.org/10.1002/ejoc.200500265openalex-snapshot
X‐ray Structure Determination, Absolute Configuration and Biological Activity of Phomoxanthone A
inferredcites →https://doi.org/10.1002/ejoc.200500887openalex-snapshot
The Domino Oxa‐Michael Addition–Aldol Reaction: Access to Variably Substituted Tetrahydroxanthenones
inferredcites →https://doi.org/10.1002/ejoc.200600789openalex-snapshot
Absolute Configurations of Globosuxanthone A and Secondary Metabolites from Microdiplodia sp. – A Novel Solid‐State CD/TDDFT Approach
inferredcites →https://doi.org/10.1002/ejoc.200700839openalex-snapshot
Isofusidienols: Novel Chromone‐3‐oxepines Produced by the Endophytic Fungus Chalara sp.
inferredcites →https://doi.org/10.1002/ejoc.200900635openalex-snapshot
Probing the Oxidation of Functionalized (Hexahydro)xanthenols
inferredcites →https://doi.org/10.1002/hlca.19520350632openalex-snapshot
Über gelbe Farbstoffe im Mutterkorn. 11. Mitteilung über antibakterielle Stoffe
inferredcites →https://doi.org/10.1002/hlca.19770600120openalex-snapshot
Metabolites of microorganisms. 162nd Communication. The crystal and molecular structure of lysolipin I
inferredcites →https://doi.org/10.1002/hlca.19790620732openalex-snapshot
Aktivierte Chinone: O‐ versus C‐Addition von Phenolen; eine neue, regiospezifische Synthese von Xanthonen, Thioxanthonen und N‐Methyl‐9‐acridonen
inferredcites →https://doi.org/10.1002/hlca.19840670507openalex-snapshot
Experiments on the Total Synthesis of Lysolipin I. Part I. On Configuration and Conformation of 5‐Substituted 1,2,3,4,4a,9,10,10a‐Ocathydrophenanthrene‐4,9‐diones
inferredcites →https://doi.org/10.1002/hlca.19840670713openalex-snapshot
Experiments on the total synthesis of Lysolipin I. Part II. Michael addition of 1,3‐cyclohexanedione to quinone acetals
inferredcites →https://doi.org/10.1002/hlca.19840670714openalex-snapshot
Experiments on the total synthesis of Lysolipin I. Part III. Preparation and transformations of substituted 1,2,3,4‐Tetrahydrodibenzofuran‐1‐ones
inferredcites →https://doi.org/10.1002/hlca.200900396openalex-snapshot
New Lactone and Xanthone Derivatives Produced by a Mangrove Endophytic Fungus Phoma sp. SK3RW1M from the South China Sea
inferredcites →https://doi.org/10.1002/mrc.1872openalex-snapshot
1H and 13C NMR assignments for two new xanthones from the endophytic fungus Xylaria sp. FRR 5657
inferredcites →https://doi.org/10.1002/mrc.1974openalex-snapshot
1H and 13C NMR assignments for two anthraquinones and two xanthones from the mangrove fungus (ZSUH‐36)
inferredcites →https://doi.org/10.1002/mrc.2035openalex-snapshot
1H and 13C NMR signal assignments of Paecilin A and B, two new chromone derivatives from mangrove endophytic fungus Paecilomyces sp. (tree 1–7)
inferredcites →https://doi.org/10.1002/mrc.2293openalex-snapshot
Structure elucidation of two new xanthone derivatives from the marine fungus Penicillium sp. (ZZF 32#) from the South China Sea
inferredcites →https://doi.org/10.1002/mrc.2539openalex-snapshot
Structure elucidation and NMR assignments for two xanthone derivatives from a mangrove endophytic fungus (No. ZH19)
inferredcites →https://doi.org/10.1002/pca.2800050405openalex-snapshot
Analysis of secondary metabolites from Lichen by high performance liquid chromatography with a photodiode array detector
inferredcites →https://doi.org/10.1002/prac.18980580127openalex-snapshot
Beitrag zur Kenntniss der Flechten und ihrer charakteristischen Bestandtheile
inferredcites →https://doi.org/10.1002/ps.1645openalex-snapshot
New asperxanthone and asperbiphenyl from the marine fungus Aspergillus sp.
inferredcites →https://doi.org/10.1006/cbir.1996.0068openalex-snapshot
INHIBITION OF CELLULAR GROWTH AND STEROID 11β‐HYDROXYLATION INRAS‐TRANSFORMED ADRENOCORTICAL CELLS BY THE FUNGAL TOXINS BETICOLINS
inferredcites →https://doi.org/10.1006/taap.2000.9061openalex-snapshot
Secalonic Acid D Alters the Nature of and Inhibits the Binding of the Transcription Factors to the Phorbol 12-O-Tetradecanoate-13 Acetate-Response Element in the Developing Murine Secondary Palate
inferredcites →https://doi.org/10.1007/bf00254193openalex-snapshot
Mechanism of the antitumor activity of 5,5?-bis(2?-tetrahydropyranyl) secalonic acid D against Meth-A
inferredcites →https://doi.org/10.1007/bf00409302openalex-snapshot
�ber den Wirtskreis und die systematische Verwandtschaft von Cercospora beticola
inferredcites →https://doi.org/10.1007/bf00446521openalex-snapshot
Stoffwechselprodukte von Mikroorganismen
inferredcites →https://doi.org/10.1007/bf00984667openalex-snapshot
Chemical variation in two species of theLecanora subfusca group (Lecanoraceae, lichenizedAscomycotina)
inferredcites →https://doi.org/10.1007/bf01092736openalex-snapshot
Chemical constituents of Hypogymnia enteromorpha
inferredcites →https://doi.org/10.1007/bf01456535openalex-snapshot
Lecanora vinetorum nova spec., ihre Vergesellschaftung, ihre �kologie und ihre Chemie
inferredcites →https://doi.org/10.1007/bf02880192openalex-snapshot
Bikaverin, an antibiotic fromGibberella fujikuroi, effective againstLeishmania brasiliensis
inferredcites →https://doi.org/10.1007/bf02974275openalex-snapshot
Cytotoxic activity fo four xanthones fromEmericella variecolor, an endophytic fungus isolated fromCroton oblongifolius
inferredcites →https://doi.org/10.1007/bf02977469openalex-snapshot
Secalonic acid D; A cytotoxic constituent from marine lichen-derived fungusGliocladium sp. T31
inferredcites →https://doi.org/10.1007/bf03051859openalex-snapshot
Nuclear oxidation in flavones and related compounds
inferredcites →https://doi.org/10.1007/s10600-010-9572-yopenalex-snapshot
A new xanthone from Penicillium oxalicum
inferredcites →https://doi.org/10.1016/0005-2736(94)90018-3openalex-snapshot
Cercospora beticola toxins. VII. Fluorometric study of their interactions with biological membranes
inferredcites →https://doi.org/10.1016/0006-291x(92)92308-kopenalex-snapshot
Bilayers containing calcium ionophore A23187 form channels
inferredcites →https://doi.org/10.1016/0021-9673(93)83356-wopenalex-snapshot
Identification of lichen substances by a standardized high-performance liquid chromatographic method
inferredcites →https://doi.org/10.1016/0021-9673(95)00079-3openalex-snapshot
Cercospora beticola toxins III. Purification, thin-layer and high performance liquid chromatographic analyses
inferredcites →https://doi.org/10.1016/0031-9422(75)83132-3openalex-snapshot
3,6,8-Trihydroxy-1-methylxanthone—an antibacterial metabolite from Penicillium patulum
inferredcites →https://doi.org/10.1016/0031-9422(79)80077-1openalex-snapshot
Mycochromone and mycoxanthone: Two new metabolites from Mycosphaerella rosigena
inferredcites →https://doi.org/10.1016/0031-9422(89)80170-0openalex-snapshot
Xanthones from guttiferae
inferredcites →https://doi.org/10.1016/0031-9422(93)85133-copenalex-snapshot
A Cercospora isolate from soybean roots produces cebetin B and cercosporin
inferredcites →https://doi.org/10.1016/0031-9422(96)00093-3openalex-snapshot
Cercospora beticola toxins. determination of O2− · scavenging activity of beticolin-1
inferredcites →https://doi.org/10.1016/0031-9422(96)00313-5openalex-snapshot
Cercospora beticola toxins. Use of fluorescent cyanine dye to study their effects on tobacco cell suspensions
inferredcites →https://doi.org/10.1016/0040-4020(68)88020-2openalex-snapshot
O-methylsterigmatocystin, a new metabolite from aspergillus flavus, link ex fries
inferredcites →https://doi.org/10.1016/0040-4020(70)85006-2openalex-snapshot
The isolation, structure and absolute configuration of secalonic acid D, the toxic metabolite of Penicillium oxalicum
inferredcites →https://doi.org/10.1016/0040-4020(73)80003-1openalex-snapshot
The structures of eumitrins A1, A2 and B
inferredcites →https://doi.org/10.1016/0040-4020(78)80055-6openalex-snapshot
Total syntheses of lichen xanthones
inferredcites →https://doi.org/10.1016/0040-4020(78)88377-xopenalex-snapshot
Struktur und 13C-NMR-spektroskopie von chlorhaltigen flechtenxanthonen
inferredcites →https://doi.org/10.1016/0040-4039(91)85080-oopenalex-snapshot
Hydrazino and N-Amino peptides. Chemical and structural aspects
inferredcites →https://doi.org/10.1016/0040-4039(96)00506-0openalex-snapshot
Cercospora beticola toxins. Part XI1: Isolation and structure of beticolin 0
inferredcites →https://doi.org/10.1016/0041-008x(68)90113-0openalex-snapshot
Investigations of the toxic effects in mice of certain species of Penicillium
inferredcites →https://doi.org/10.1016/0048-4059(79)90064-xopenalex-snapshot
Inhibition of K+ uptake, H+ extrusion and K+-activated ATPase, and depolarization of transmembrane potential in plant tissues treated with Cercospora beticola toxin
inferredcites →https://doi.org/10.1016/0301-4622(94)00096-3openalex-snapshot
Cercospora beticola toxins. Part VI: preliminary studies of protonation and complexation equilibria
inferredcites →https://doi.org/10.1016/0304-4211(80)90110-8openalex-snapshot
Effects of Cercospora beticola toxin on ATP level of maize roots and on the phosphorylating activity of isolated pea mitochondria
inferredcites →https://doi.org/10.1016/j.bbrc.2004.03.117openalex-snapshot
Selective inhibition of bleomycin-induced G2 cell cycle checkpoint by simaomicin α
inferredcites →https://doi.org/10.1016/j.bmc.2006.07.048openalex-snapshot
A new dihydroxanthenone from a plant-associated strain of the fungus Chaetomium globosum demonstrates anticancer activity
inferredcites →https://doi.org/10.1016/j.bmcl.2008.12.081openalex-snapshot
Isolation and structure elucidation of parnafungins C and D, isoxazolidinone-containing antifungal natural products
inferredcites →https://doi.org/10.1016/j.canlet.2006.01.018openalex-snapshot
Signal therapy of human pancreatic cancer and NF1-deficient breast cancer xenograft in mice by a combination of PP1 and GL-2003, anti-PAK1 drugs (Tyr-kinase inhibitors)
inferredcites →https://doi.org/10.1016/j.chembiol.2008.02.016openalex-snapshot
PAP Inhibitor with In Vivo Efficacy Identified by Candida albicans Genetic Profiling of Natural Products
inferredcites →https://doi.org/10.1016/j.fitote.2004.04.002openalex-snapshot
Intermediate reactive oxygen and nitrogen from macrophages induced by Brazilian lichens
inferredcites →https://doi.org/10.1016/j.phymed.2009.07.018openalex-snapshot
Antimycobacterial activity of lichen substances
inferredcites →https://doi.org/10.1016/j.phytochem.2004.12.031openalex-snapshot
Monomeric and dimeric dibenzofurans from cultured mycobionts of Lecanora iseana
inferredcites →https://doi.org/10.1016/j.phytochem.2007.09.006openalex-snapshot
Metabolites from the endophytic fungus Phomopsis sp. PSU-D15
inferredcites →https://doi.org/10.1016/j.tet.2008.08.038openalex-snapshot
Microsphaerins A–D, four novel benzophenone dimers with activity against MRSA from the fungus Microsphaeropsis sp.
inferredcites →https://doi.org/10.1016/j.tetlet.2007.05.151openalex-snapshot
Anhydrocochlioquinone A, a new antitumor compound from Bipolaris oryzae
inferredcites →https://doi.org/10.1016/j.tetlet.2008.10.146openalex-snapshot
Acremoxanthones A and B, novel antibiotic polyketides from the fungus Acremonium sp. BCC 31806
inferredcites →https://doi.org/10.1016/j.tetlet.2009.06.008openalex-snapshot
Isolation, structure elucidation, and biological evaluation of the unusual heterodimer chrysoxanthone from the ascomycete IBWF11-95A
inferredcites →https://doi.org/10.1016/j.tox.2004.05.007openalex-snapshot
Cytotoxicity of occupationally and environmentally relevant mycotoxins
inferredcites →https://doi.org/10.1016/j.ympev.2004.04.014openalex-snapshot
Molecular phylogeny of the Pertusariaceae supports secondary chemistry as an important systematic character set in lichen-forming ascomycetes
inferredcites →https://doi.org/10.1016/s0005-2736(96)00144-7openalex-snapshot
Cercospora beticola toxins. Part XVII. The role of the beticolin/Mg2+ complexes in their biological activity Study of plasma membrane H+-ATPase, vacuolar H+-PPase, alkaline and acid phosphatases
inferredcites →https://doi.org/10.1016/s0006-3495(99)77136-5openalex-snapshot
Cluster Organization and Pore Structure of Ion Channels Formed by Beticolin 3, a Nonpeptidic Fungal Toxin
inferredcites →https://doi.org/10.1016/s0007-1536(69)80128-2openalex-snapshot
Observations on induced vacuoles in fungi
inferredcites →https://doi.org/10.1016/s0014-5793(96)01218-5openalex-snapshot
Activation of the plant plasma membrane H+‐ATPase. Is there a direct interaction between lysophosphatidylcholine and the C‐terminal part of the enzyme?
inferredcites →https://doi.org/10.1016/s0014-5793(97)00405-5openalex-snapshot
Xanthones as antimalarial agents; studies of a possible mode of action
inferredcites →https://doi.org/10.1016/s0021-9673(00)87954-6openalex-snapshot
High-performance liquid chromatographic analysis of the mycotoxin secalonic acid d and its application to biological fluids
inferredcites →https://doi.org/10.1016/s0021-9673(03)00501-6openalex-snapshot
Identification of acylated xanthone glycosides by liquid chromatography–atmospheric pressure chemical ionization mass spectrometry in positive and negative modes from the lichen Umbilicaria proboscidea
inferredcites →https://doi.org/10.1016/s0031-9422(00)00303-4openalex-snapshot
Tetraoxygenated naturally occurring xanthones
inferredcites →https://doi.org/10.1016/s0031-9422(00)86530-9openalex-snapshot
Isolation of bikaverin from Mycogone jaapii
inferredcites →https://doi.org/10.1016/s0031-9422(00)86794-1openalex-snapshot
Screening of the genus Cercospora for secondary metabolites☆
inferredcites →https://doi.org/10.1016/s0031-9422(00)88089-9openalex-snapshot
Xanthones in higher plants: Biogenetic proposals and a chemotaxonomic survey
inferredcites →https://doi.org/10.1016/s0031-9422(00)90881-1openalex-snapshot
Biogenetic proposals regarding aucuparins and xanthones
inferredcites →https://doi.org/10.1016/s0031-9422(00)94841-6openalex-snapshot
Triterpenes, lichexanthone and an acetylenic acid from Minquartia guianensis
inferredcites →https://doi.org/10.1016/s0031-9422(00)97499-5openalex-snapshot
A new phthalide and xanthones from Anthocleista djalonensis and Anthocleista vogelli
inferredcites →https://doi.org/10.1016/s0031-9422(00)97907-xopenalex-snapshot
A chromone from Zanthoxylum species
inferredcites →https://doi.org/10.1016/s0031-9422(01)00278-3openalex-snapshot
Phytotoxic naphthopyranone derivatives from the coprophilous fungus Guanomyces polythrix
inferredcites →https://doi.org/10.1016/s0031-9422(02)00539-3openalex-snapshot
Prenylated xanthone glucosides from Ural's lichen Umbilicaria proboscidea
inferredcites →https://doi.org/10.1016/s0031-9422(03)00189-4openalex-snapshot
Evariquinone, isoemericellin, and stromemycin from a sponge derived strain of the fungus Emericella variecolor
inferredcites →https://doi.org/10.1016/s0031-9422(96)00421-9openalex-snapshot
Trioxygenated naturally occurring xanthones
inferredcites →https://doi.org/10.1016/s0031-9422(98)00169-1openalex-snapshot
Neosartorin, an ergochrome biosynthesized by Neosartorya fischeri
inferredcites →https://doi.org/10.1016/s0040-4020(01)83114-8openalex-snapshot
Xanthonoids of tropical plants
inferredcites →https://doi.org/10.1016/s0040-4020(01)85666-0openalex-snapshot
Total synthesis of novel xanthone antibiotics (±)-cervinomycins A1, and A2
inferredcites →https://doi.org/10.1016/s0040-4020(01)98098-6openalex-snapshot
Biogenetic-type synthesis of polyketides. Part X
inferredcites →https://doi.org/10.1016/s0040-4039(00)60324-6openalex-snapshot
The yellow toxins produced by Cercospora beticola. Part II: Isolation and structure of beticolins 3 and 4
inferredcites →https://doi.org/10.1016/s0040-4039(00)61403-xopenalex-snapshot
The structure of xanthoquinodin A1, a novel anticoccidial antibiotic having a new xanthone-anthraquinone conjugate system
inferredcites →https://doi.org/10.1016/s0040-4039(00)78501-7openalex-snapshot
The yellow toxins produced by Cercospora Beticola. Part VIII : Chemical equilibrium between beticolins ; structures of minor compounds : beticolin 6 and beticolin 8
inferredcites →https://doi.org/10.1016/s0040-4039(00)78863-0openalex-snapshot
New total synthesis of bikaverin
inferredcites →https://doi.org/10.1016/s0040-4039(00)90148-5openalex-snapshot
Ergochrome, eine ungewöhnlich vollständige gruppe dimerer farbstoffe aus claviceps purpurea
inferredcites →https://doi.org/10.1016/s0040-4039(00)90972-9openalex-snapshot
Incorporation of shikimic acid into 1,2-dihydroxy-anthraquinone (alizarin) by L.
inferredcites →https://doi.org/10.1016/s0040-4039(00)91207-3openalex-snapshot
Biosynthesis of ravenelin from [1-13C]-acetate
inferredcites →https://doi.org/10.1016/s0040-4039(00)92295-0openalex-snapshot
Structure of a novel phospholipase C inhibitor, vinaxanthone (Ro 09-1450), produced by penicillium vinaceum
inferredcites →https://doi.org/10.1016/s0040-4039(00)93465-8openalex-snapshot
Total synthesis of cervinomycin A1-trimethyl ether and cervinomycin A2-methyl ether
inferredcites →https://doi.org/10.1016/s0040-4039(00)99436-xopenalex-snapshot
Extended scope of the grignard reaction of β-haloacetals. Use of acyclic acetals
inferredcites →https://doi.org/10.1016/s0040-4039(01)82826-4openalex-snapshot
Flechteninhaltsstoffe XXXII thiophansäure, ein neues chlorhaltiges xanthon aus (L.) zahlbr.
inferredcites →https://doi.org/10.1016/s0040-4039(01)83067-7openalex-snapshot
5,6-dimethoxysterigmatocystin, a new metabolite from aspergillus multicolor
inferredcites →https://doi.org/10.1016/s0040-4039(01)85259-xopenalex-snapshot
The structure of albofungin
inferredcites →https://doi.org/10.1016/s0040-4039(01)85690-2openalex-snapshot
A new secalonic acid. Linkage between tetrahydroxanthone units determined from deuterium isotope 13C chemical shifts
inferredcites →https://doi.org/10.1016/s0040-4039(01)87529-8openalex-snapshot
Total synthesis of (±)-dihydro-o-methylsterigmatocystin
inferredcites →https://doi.org/10.1016/s0040-4039(01)90105-4openalex-snapshot
Synthesis of cis-bicyco¦13.3.0¦oct-3-ene-2,7-dione, a highly functionalized cyclopentanoid intermediate
inferredcites →https://doi.org/10.1016/s0040-4039(01)91747-2openalex-snapshot
The stereochemistry of albofungin
inferredcites →https://doi.org/10.1016/s0040-4039(01)92200-2openalex-snapshot
Utilization of 13C-13C coupling in structural and biosynthetic studies V. The 13C ft nmr spectrum of sterigmatocystin
inferredcites →https://doi.org/10.1016/s0040-4039(01)99251-2openalex-snapshot
Principe et applications d'une nouvelle methode de determination des configurations dite “par dedoublement partiel”
inferredcites →https://doi.org/10.1016/s0040-4039(03)01318-2openalex-snapshot
Xantholipin, a novel inhibitor of HSP47 gene expression produced by Streptomyces sp.
inferredcites →https://doi.org/10.1016/s0040-4039(97)00642-4openalex-snapshot
Synthesis of arylboronates via the palladium(0)-catalyzed cross-coupling reaction of tetra(alkoxo)diborons with aryl triflates
inferredcites →https://doi.org/10.1016/s0146-6380(02)00015-3openalex-snapshot
Xanthones—novel aromatic oxygen-containing compounds in crude oils
inferredcites →https://doi.org/10.1016/s0928-0987(97)00078-xopenalex-snapshot
Antimycobacterial activity of lichen metabolites in vitro
inferredcites →https://doi.org/10.1016/s0960-894x(99)00440-0openalex-snapshot
Syntheses of novel antitumor dihydroxanthone derivatives with inhibitory activity against DNA topoisomerase II
inferredcites →https://doi.org/10.1016/s0981-9428(02)00017-7openalex-snapshot
Differences in the composition of phenolics and fatty acids of cultured mycobiont and thallus of Physconia distorta
inferredcites →https://doi.org/10.1021/cr050001fopenalex-snapshot
Chemistry and Biology of Mycotoxins and Related Fungal Metabolites
inferredcites →https://doi.org/10.1021/cr960032yopenalex-snapshot
Enzymology and Molecular Biology of Aflatoxin Biosynthesis
inferredcites →https://doi.org/10.1021/ja00030a051openalex-snapshot
Structures of the beticolins, the yellow toxins produced by Cercospora beticola
inferredcites →https://doi.org/10.1021/ja00041a009openalex-snapshot
Cercospora beticola phytotoxins: cebetins that are photoactive, magnesium ion-binding, chlorinated anthraquinone-xanthone conjugates
inferredcites →https://doi.org/10.1021/ja00072a006openalex-snapshot
Structure and biosynthesis of xanthoquinodins, anticoccidial antibiotics
inferredcites →https://doi.org/10.1021/ja00194a071openalex-snapshot
Synthesis of (.+-.)cervinomycins A1 and A2
inferredcites →https://doi.org/10.1021/ja00279a095openalex-snapshot
Structure of cervinomycin, a novel antianaerobic antibiotic
inferredcites →https://doi.org/10.1021/ja00352a044openalex-snapshot
Cyclohexanone oxygenase: stereochemistry, enantioselectivity, and regioselectivity of an enzyme-catalyzed Baeyer-Villiger reaction
inferredcites →https://doi.org/10.1021/ja00370a055openalex-snapshot
Fungal xanthone biosynthesis. Distribution of acetate-derived oxygens in ravenelin
inferredcites →https://doi.org/10.1021/ja01082a031openalex-snapshot
The Structures of Aflatoxins B and G1
inferredcites →https://doi.org/10.1021/ja01169a067openalex-snapshot
The Two-Step Reduction--Oxidation of Thiaxanthone-5-dioxide and Thiaxanthenol-5-dioxide
inferredcites →https://doi.org/10.1021/ja012185vopenalex-snapshot
Synthesis of 11-Hydroxyl O-Methylsterigmatocystin and the Role of a Cytochrome P-450 in the Final Step of Aflatoxin Biosynthesis
inferredcites →https://doi.org/10.1021/ja01578a038openalex-snapshot
Cercosporin. A Pigment of Cercosporina Kikuchii Matsumoto et Tomoyasu. I. Cultivation of Fungus, Isolation and Purification of Pigment
inferredcites →https://doi.org/10.1021/ja0202255openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reaction of Bis(pinacolato)diboron with 1-Alkenyl Halides or Triflates: Convenient Synthesis of Unsymmetrical 1,3-Dienes via the Borylation-Coupling Sequence
inferredcites →https://doi.org/10.1021/ja0455188openalex-snapshot
Ordering the Reductive and Cytochrome P450 Oxidative Steps in Demethylsterigmatocystin Formation Yields General Insights into the Biosynthesis of Aflatoxin and Related Fungal Metabolites
inferredcites →https://doi.org/10.1021/ja1015926openalex-snapshot
An “End-On” Chromium(III)-Superoxo Complex: Crystallographic and Spectroscopic Characterization and Reactivity in C−H Bond Activation of Hydrocarbons
inferredcites →https://doi.org/10.1021/ja110698nopenalex-snapshot
Vinylogous Addition of Siloxyfurans to Benzopyryliums: A Concise Approach to the Tetrahydroxanthone Natural Products
inferredcites →https://doi.org/10.1021/ja711209popenalex-snapshot
Isolation and Structure Elucidation of Parnafungins, Antifungal Natural Products that Inhibit mRNA Polyadenylation
inferredcites →https://doi.org/10.1021/ja805531wopenalex-snapshot
Application of Affinity Selection/Mass Spectrometry to Determine the Structural Isomer of Parnafungins Responsible for Binding Polyadenosine Polymerase
inferredcites →https://doi.org/10.1021/jm00233a018openalex-snapshot
Preparation and antitumor activities of some derivatives of 5-methoxysterigmatocystin
inferredcites →https://doi.org/10.1021/jm100319hopenalex-snapshot
Novel Highly Potent and Selective Nonsteroidal Aromatase Inhibitors: Synthesis, Biological Evaluation and Structure−Activity Relationships Investigation
inferredcites →https://doi.org/10.1021/jo00087a021openalex-snapshot
Biosynthetic studies on the xanthone antibiotics lysolipins X and I
inferredcites →https://doi.org/10.1021/jo00128a024openalex-snapshot
Palladium(0)-Catalyzed Cross-Coupling Reaction of Alkoxydiboron with Haloarenes: A Direct Procedure for Arylboronic Esters
inferredcites →https://doi.org/10.1021/jo00236a055openalex-snapshot
Regiospecific preparation of the benz[b]xanthen-12-one ring system. Total synthesis of bikaverin
inferredcites →https://doi.org/10.1021/jo00279a018openalex-snapshot
Biosynthetic origin of the carbon skeleton of simaomicin .alpha., a hexacyclic xanthone antibiotic
inferredcites →https://doi.org/10.1021/jo00302a011openalex-snapshot
A complex induced proximity effect in the anionic Fries rearrangement of o-iodophenyl benzoates: synthesis of dihydro-O-methylsterigmatocystin and other xanthones
inferredcites →https://doi.org/10.1021/jo00324a012openalex-snapshot
Acylation of multiple anions of poly-.beta.-ketones by hydroxy- and alkoxybenzoates. Cyclization of the resultant tetraketones to benzophenones and xanthones
inferredcites →https://doi.org/10.1021/jo00422a042openalex-snapshot
Secalonic acids D and F are toxic metabolites of Aspergillus aculeatus
inferredcites →https://doi.org/10.1021/jo01338a046openalex-snapshot
Synthesis of pinselic acid and pinselin
inferredcites →https://doi.org/10.1021/jo0490393openalex-snapshot
A New Protocol for the One-Pot Synthesis of Symmetrical Biaryls
inferredcites →https://doi.org/10.1021/jo101826popenalex-snapshot
Synthesis of Hexacyclic Parnafungin A and C Models
inferredcites →https://doi.org/10.1021/jo101873vopenalex-snapshot
CAN-Mediated Oxidations for the Synthesis of Xanthones and Related Products
inferredcites →https://doi.org/10.1021/jo961267copenalex-snapshot
Pores Formed by Bis-macrocyclic Bola-amphiphiles in Vesicle and Planar Bilayer Membranes
inferredcites →https://doi.org/10.1021/jo982182+openalex-snapshot
Unique Solvent-Dependent Atropisomerism of a Novel Cytotoxic Naphthoxanthene Antibiotic FD-594
inferredcites →https://doi.org/10.1021/jo990099wopenalex-snapshot
Total Synthesis of O -Methylsterigmatocystin Using N -Alkylnitrilium Salts and Carbonyl−Alkene Interconversion in a New Xanthone Synthesis
inferredcites →https://doi.org/10.1021/np010006hopenalex-snapshot
Phomoxanthones A and B, Novel Xanthone Dimers from the Endophytic Fungus Phomopsis Species
inferredcites →https://doi.org/10.1021/np010020uopenalex-snapshot
Dicerandrols, New Antibiotic and Cytotoxic Dimers Produced by the Fungus Phomopsis longicolla Isolated from an Endangered Mint
inferredcites →https://doi.org/10.1021/np010092lopenalex-snapshot
Rare Sesquiterpenes from the Algicolous Fungus Drechslera dematioidea
inferredcites →https://doi.org/10.1021/np0103214openalex-snapshot
Bioactive Metabolites from a Marine-Derived Strain of the Fungus Emericella variecolor
inferredcites →https://doi.org/10.1021/np020295popenalex-snapshot
Bioactive Natural Products from a Sclerotium-Colonizing Isolate of Humicola fuscoatra
inferredcites →https://doi.org/10.1021/np020518bopenalex-snapshot
Two New Xanthone Derivatives from the Algicolous Marine Fungus Wardomyces anomalus
inferredcites →https://doi.org/10.1021/np034038bopenalex-snapshot
Rugulotrosins A and B: Two New Antibacterial Metabolites from an Australian Isolate of a Penicillium sp.
inferredcites →https://doi.org/10.1021/np058028hopenalex-snapshot
A Cytotoxic Xanthone Dimer from the Entomopathogenic Fungus Aschersonia sp. BCC 8401
inferredcites →https://doi.org/10.1021/np060505oopenalex-snapshot
Potential Cancer Chemopreventive in Vitro Activities of Monomeric Xanthone Derivatives from the Marine Algicolous Fungus Monodictys putredinis
inferredcites →https://doi.org/10.1021/np070079mopenalex-snapshot
Hirtusneanoside, an Unsymmetrical Dimeric Tetrahydroxanthone from the Lichen Usnea hirta
inferredcites →https://doi.org/10.1021/np1000335openalex-snapshot
Polyketides from the Ascomycete Fungus Leptosphaeria sp.
inferredcites →https://doi.org/10.1021/np100071zopenalex-snapshot
Oxepinochromenones, Furochromenone, and their Putative Precursors from the Endolichenic Fungus Coniochaeta sp.
inferredcites →https://doi.org/10.1021/np100730bopenalex-snapshot
Diversonol and Blennolide Derivatives from the Endophytic Fungus Microdiplodia sp.: Absolute Configuration of Diversonol
inferredcites →https://doi.org/10.1021/np50061a015openalex-snapshot
Metabolites of Leptographium wageneri, the Causative Agent of Black Stain Root Disease of Conifers
inferredcites →https://doi.org/10.1021/np800020popenalex-snapshot
A Biaryl Xanthone Derivative Having Axial Chirality from Penicillium vinaceum
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112895zenodo-depositor-declared
A comprehensive review: Biological activity, modification and synthetic methodologies of prenylated flavonoids
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Xanthones from Marine‐Derived Microorganisms: Isolation, Structure Elucidation and Biological Activities
inferred← citeshttps://doi.org/10.1002/9781119593249.ch1openalex-snapshot
An Overview on Lichen's Morphology, Chemistry of Derived Products, and Current Scenario
inferred← citeshttps://doi.org/10.1002/adsc.201300750openalex-snapshot
Synthesis of 4‐Aminoxanthones by an Uncatalyzed, Multicomponent Reaction
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Enantioselective Cascade Oxa‐Michael–Michael Reactions of 2‐Hydroxynitrostyrenes with Enones Using a Prolinol Thioether Catalyst
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Stannylation and Stille Coupling of Base‐Sensitive Tetrahydroxanthones to Heteromeric Biaryls
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Allene‐Based Gold‐Catalyzed Stereodivergent Synthesis of Azapolycyclic Derivatives of Unusual Structure
inferred← citeshttps://doi.org/10.1002/adsc.201601296openalex-snapshot
Rhodium(III)‐Catalyzed Cascade Redox‐Neutral C–H Functionalization and Aromatization: Synthesis of Unsymmetrical ortho‐Biphenols
inferred← citeshttps://doi.org/10.1002/adsc.201700400openalex-snapshot
Decarboxylative Aminocatalytic Cascade for the Synthesis of Dihydroxanthones
inferred← citeshttps://doi.org/10.1002/adsc.201900119openalex-snapshot
Organocatalytic Michael/Michael Cycloaddition Enabled Asymmetric Construction of Hexahydroxanthones with Skeletal Diversity
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Dienolate‐Mediated, Regioselective C2‐Polarity Reversal of Chromone‐Based Reactants and Their Application in Nucleophilic Strategies
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Organocatalytic oxa‐Michael/Michael Addition/Deformylation Cascade Reaction of 3‐Formylchromone with p‐Quinol: Synthesis of the Furanochromanone Skeleton
inferred← citeshttps://doi.org/10.1002/adsc.202400113openalex-snapshot
The Asymmetric Synthesis of Polycyclic Tetrahydroxanthone via the Cascade Reaction of Alkene‐Substituted 1,3‐diketones and Alkenyloxindoles
inferred← citeshttps://doi.org/10.1002/adsc.202400378openalex-snapshot
In(OTf)3‐Catalyzed Diastereoselective [2+3+1] Annulation of 3‐Formylchromones with α‐Methylstyrenes for Divergent Synthesis of Tetrahydroxanthones
inferred← citeshttps://doi.org/10.1002/ajoc.201900166openalex-snapshot
Carboxylic‐Acid‐Activated Olefins in Decarboxylative Reactions
inferred← citeshttps://doi.org/10.1002/ange.201204790openalex-snapshot
Enantioselective H‐Bond‐Directing Approach for Trienamine‐mediated Reactions in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/ange.201207485openalex-snapshot
Das Acetal‐Konzept: regioselektiver Zugang zu ortho,ortho‐Diphenolen über Dibenzo‐1,3‐dioxepine
inferred← citeshttps://doi.org/10.1002/ange.201311260openalex-snapshot
Total Syntheses of Secalonic Acids A and D
inferred← citeshttps://doi.org/10.1002/ange.201402384openalex-snapshot
Doppelt genäht hält besser – die Kunst der Synthese chiraler dimerer Naturstoffe
inferred← citeshttps://doi.org/10.1002/ange.201503538openalex-snapshot
Vier‐ und sechsfache Tandem‐Dominoreaktionen zur Synthese von dimeren tetrasubstituierten Alkenen als molekulare Doppelschalter
inferred← citeshttps://doi.org/10.1002/ange.201801612openalex-snapshot
Cascade Claisen Rearrangement: Rapid Synthesis of Polysubstituted Salicylaldehydes and Total Syntheses of Hemigossypol and Gossypol
inferred← citeshttps://doi.org/10.1002/ange.201915787openalex-snapshot
Asymmetric Total Synthesis of the Complex Polycyclic Xanthone FD‐594
inferred← citeshttps://doi.org/10.1002/ange.202107884openalex-snapshot
Structural Basis for Isomerization Reactions in Fungal Tetrahydroxanthone Biosynthesis and Diversification
inferred← citeshttps://doi.org/10.1002/ange.202203128openalex-snapshot
Concise and Stereodivergent Approach to Chromanone Lactones through Copper‐Catalyzed Asymmetric Vinylogous Addition of Siloxyfurans to 2‐Ester‐Substituted Chromones
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Visible‐Light Photocatalyzed Skeletal Rearrangement Enables the Synthesis of Highly Functionalized Xanthenes with Antitumor Activity
inferred← citeshttps://doi.org/10.1002/ange.8287171openalex-snapshot
Synthesis and Property Study on Homoaromatic Thiabenzenes
inferred← citeshttps://doi.org/10.1002/anie.201204790openalex-snapshot
Enantioselective H‐Bond‐Directing Approach for Trienamine‐mediated Reactions in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201207485openalex-snapshot
The Acetal Concept: Regioselective Access to ortho,ortho‐Diphenols via Dibenzo‐1,3‐dioxepines
inferred← citeshttps://doi.org/10.1002/anie.201311260openalex-snapshot
Total Syntheses of Secalonic Acids A and D
inferred← citeshttps://doi.org/10.1002/anie.201402384openalex-snapshot
Double Trouble—The Art of Synthesis of Chiral Dimeric Natural Products
inferred← citeshttps://doi.org/10.1002/anie.201503538openalex-snapshot
Four‐ and Sixfold Tandem‐Domino Reactions Leading to Dimeric Tetrasubstituted Alkenes Suitable as Molecular Switches
inferred← citeshttps://doi.org/10.1002/anie.201801612openalex-snapshot
Cascade Claisen Rearrangement: Rapid Synthesis of Polysubstituted Salicylaldehydes and Total Syntheses of Hemigossypol and Gossypol
inferred← citeshttps://doi.org/10.1002/anie.201915787openalex-snapshot
Asymmetric Total Synthesis of the Complex Polycyclic Xanthone FD‐594
inferred← citeshttps://doi.org/10.1002/anie.202107884openalex-snapshot
Structural Basis for Isomerization Reactions in Fungal Tetrahydroxanthone Biosynthesis and Diversification
inferred← citeshttps://doi.org/10.1002/anie.202203128openalex-snapshot
Concise and Stereodivergent Approach to Chromanone Lactones through Copper‐Catalyzed Asymmetric Vinylogous Addition of Siloxyfurans to 2‐Ester‐Substituted Chromones
inferred← citeshttps://doi.org/10.1002/anie.202420671openalex-snapshot
Visible‐Light Photocatalyzed Skeletal Rearrangement Enables the Synthesis of Highly Functionalized Xanthenes with Antitumor Activity
inferred← citeshttps://doi.org/10.1002/anie.8287171openalex-snapshot
Synthesis and Property Study on Homoaromatic Thiabenzenes
inferred← citeshttps://doi.org/10.1002/ardp.202000156openalex-snapshot
Probing simple structural modification of α‐mangostin on its cholinesterase inhibition and cytotoxicity
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Enantioselective Total Synthesis of Chromanone Lactone Homo‐ and Heterodimers
inferred← citeshttps://doi.org/10.1002/bmc.3802openalex-snapshot
Quantification of 1‐(propan‐2‐ylamino)‐4‐propoxy‐9H‐thioxanthen‐9‐one (TX5), a newly synthetized P‐glycoprotein inducer/activator, in biological samples: method development and validation
inferred← citeshttps://doi.org/10.1002/cbdv.201900499openalex-snapshot
Xanthones and Cancer: from Natural Sources to Mechanisms of Action
inferred← citeshttps://doi.org/10.1002/cbdv.202200507openalex-snapshot
Natural Compounds with Oxepinochromene Scaffold. Structure, Source, Biological Activity and Synthesis
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A Review of the Chemistry and Biological Activities of Natural Colorants, Dyes, and Pigments: Challenges, and Opportunities for Food, Cosmetics, and Pharmaceutical Application
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Antioxidant and Antimicrobial Activities of 4 H ‐Chromene Based Indole‐Pyrimidine Hybrids: Synthesis and Molecular Docking Studies
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New Insights into the Biosynthesis of Prenylated Xanthones: Xptb from Aspergillus nidulans Catalyses an O‐Prenylation of Xanthones
inferred← citeshttps://doi.org/10.1002/cbic.202200586openalex-snapshot
Biosynthetic Pathways of Dimeric Natural Products Containing Bisanthraquinone and Related Xanthones
inferred← citeshttps://doi.org/10.1002/cctc.202401552openalex-snapshot
Siloxyflavylium Triflates as Organic Photocatalysts
inferred← citeshttps://doi.org/10.1002/chem.201204037openalex-snapshot
Enantioselective Total Synthesis of (−)‐Diversonol
inferred← citeshttps://doi.org/10.1002/chem.201301358openalex-snapshot
A Radical Access to Highly Functionalized Tetrahydroxanthones
inferred← citeshttps://doi.org/10.1002/chem.201301969openalex-snapshot
Tethering for Selective Synthesis of 2,2′‐Biphenols: The Acetal Method
inferred← citeshttps://doi.org/10.1002/chem.201402495openalex-snapshot
A Domino Approach to the Enantioselective Total Syntheses of Blennolide C and Gonytolide C
inferred← citeshttps://doi.org/10.1002/chem.201503593openalex-snapshot
Enantioselective Total Synthesis of Secalonic Acid E
inferred← citeshttps://doi.org/10.1002/chem.201602064openalex-snapshot
Base‐Promoted Tandem Reaction Involving Insertion into Carbon–Carbon σ‐Bonds: Synthesis of Xanthone and Chromone Derivatives
inferred← citeshttps://doi.org/10.1002/chem.201701009openalex-snapshot
Fused Multifunctionalized Chromenes from Tetraynes and α,β‐Unsaturated Aldehydes
inferred← citeshttps://doi.org/10.1002/chem.201801323openalex-snapshot
Enantioselective Total Synthesis of Blennolide H and Phomopsis‐H76 A and Determination of Their Structure
inferred← citeshttps://doi.org/10.1002/chem.201904822openalex-snapshot
Copper Bis(oxazoline)‐Catalyzed Enantioselective Alkynylation of Benzopyrylium Ions
inferred← citeshttps://doi.org/10.1002/chem.202202397openalex-snapshot
Phomoxanthone A Targets ATP Synthase
inferred← citeshttps://doi.org/10.1002/chem.202300941openalex-snapshot
A Common C2‐Symmetric 2,2’‐Biphenol Building Block and its Application in the Synthesis of (+)‐di‐epi‐Gonytolide A
inferred← citeshttps://doi.org/10.1002/chin.201238249openalex-snapshot
ChemInform Abstract: Xanthones from Fungi, Lichens, and Bacteria: The Natural Products and Their Synthesis
inferred← citeshttps://doi.org/10.1002/chir.22703openalex-snapshot
Resolution, determination of enantiomeric purity and chiral recognition mechanism of new xanthone derivatives on (S,S)‐whelk‐O1 stationary phase
inferred← citeshttps://doi.org/10.1002/chir.22706openalex-snapshot
New chiral stationary phases based on xanthone derivatives for liquid chromatography
inferred← citeshttps://doi.org/10.1002/cjoc.202100026openalex-snapshot
Antiosteoporotic Tetrahydroxanthone Dimers from Aspergillus brunneoviolaceus FB ‐2 Residing in Human Gut
inferred← citeshttps://doi.org/10.1002/ejoc.201300752openalex-snapshot
A Stereoselective Approach to Functionalized Cyclohexenones
inferred← citeshttps://doi.org/10.1002/ejoc.201301763openalex-snapshot
Naphthoquinone Diels–Alder Reactions: Approaches to the ABC Ring System of Beticolin
inferred← citeshttps://doi.org/10.1002/ejoc.201402984openalex-snapshot
Biosynthetically Distinct Cytotoxic Polyketides from Setophoma terrestris
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Synthetic Route to 4,4a‐ and 3,4‐Dihydroxanthones through [4+2] Cycloaddition and Base‐Assisted Sigmatropic Rearrangement
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One‐Pot Organocatalytic Michael Addition/I2‐Mediated Cyclization Sequence: Metal‐Free Synthesis of Spiropyrazolones from 1,3‐Diketones and Unsaturated Pyrazolones
inferred← citeshttps://doi.org/10.1002/ejoc.201801110openalex-snapshot
Utilization of Chromone‐3‐Carboxylic Acids as Acceptors in the Michael‐Type Decarboxylative Addition
inferred← citeshttps://doi.org/10.1002/ejoc.201900370openalex-snapshot
Tf2NH catalyzed 1,6‐conjugate addition of 2‐hydroxy‐p‐quinone methides with β‐Functionalized Ketones: Access to 2,3,4,9‐Tetrahydro‐1H‐xanthenones and 4H‐Chromene Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201900745openalex-snapshot
Copper‐Catalyzed One‐Pot Synthesis of Dibenzofurans, Xanthenes, and Xanthones from Cyclic Diphenyl Iodoniums
inferred← citeshttps://doi.org/10.1002/ejoc.201901026openalex-snapshot
Synthesis and Anticancer Activity of Structure Simplified Naturally Inspired Dimeric Chromenone Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202000465openalex-snapshot
Second Generation Total Synthesis of (–)‐Preussochromone D
inferred← citeshttps://doi.org/10.1002/ejoc.202000470openalex-snapshot
Organocatalytic Synthesis of Chiral Spirooxindoles with Quaternary Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/ejoc.202200201openalex-snapshot
Chromanone Lactones: A Neglected Group of Natural Products – Isolation, Structure Elucidation, Bioactivity, and Synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.202300364openalex-snapshot
Copper‐Catalyzed Intramolecular SEAr Reaction–Oxidation under Aerobic Conditions: Synthesis of Styryl‐/Alkenyl‐Substituted Xanthone Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.70529openalex-snapshot
Metal‐Free [4‐OH‐TEMPO] + [NO 3 ] − ‐Catalyzed Aerobic Oxidation of Benzylic C(sp 3 )–H Bonds in Ethers
inferred← citeshttps://doi.org/10.1002/hlca.201400296openalex-snapshot
Three New Xanthones from the Fungus Penicillium sp. NH‐7‐1
inferred← citeshttps://doi.org/10.1002/jccs.201900214openalex-snapshot
Intramolecular cross‐dehydrogenative coupling of benzaldehyde derivatives: A novel and efficient route to benzocyclic ketones
inferred← citeshttps://doi.org/10.1002/jhet.70057openalex-snapshot
Synthesis and Cellular Evaluation of Some Oxepino‐ and Pyranoxanthone Derivatives as Antitumor Agents: A Comparative Study
inferred← citeshttps://doi.org/10.1002/mrc.3903openalex-snapshot
Three new xanthone derivatives from an algicolous isolate of Aspergillus wentii
inferred← citeshttps://doi.org/10.1002/open.202400395openalex-snapshot
Electrochemically Induced, Metal Free Synthesis of 2‐substituted chroman‐4‐ones
inferred← citeshttps://doi.org/10.1002/pca.70043openalex-snapshot
Dereplicative Combination of HPLC/DAD/MS and 2D NMR to Identify Lichexanthone Isomers in Lichen Extracts
inferred← citeshttps://doi.org/10.1002/slct.201700667openalex-snapshot
Scope and Limitations of the Domino Vinylogous Aldol/oxa‐Michael Reaction
inferred← citeshttps://doi.org/10.1002/slct.201900579openalex-snapshot
The First Vinylogous, Decarboxylative Michael Reaction with 3‐Cyano‐4‐methylcoumarins as Pronucleophiles
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Synthesis of New Chiral Derivatives of Xanthones with Enantioselective Effect on Tumor Cell Growth and DNA Crosslinking
inferred← citeshttps://doi.org/10.1002/slct.202101394openalex-snapshot
One‐Pot Synthesis of Xanthone by Carbonylative Suzuki Coupling Reaction
inferred← citeshttps://doi.org/10.1002/slct.202203340openalex-snapshot
Synthesis of Chromone‐Spiroindolinone‐Cyclopentene Derivatives through Phosphine‐Catalyzed (3+2) Annulation of Morita‐Baylis‐Hillman Carbonates with Oxindole‐Chromones
inferred← citeshttps://doi.org/10.1002/slct.202302823openalex-snapshot
Highly Diastereoselective Synthesis of Multifunctionalized Dihydrofurans by a K 3 PO 4 ‐Promoted Michael Addition‐Alkylation Reaction
inferred← citeshttps://doi.org/10.1002/slct.202303643openalex-snapshot
Transition‐Metal Catalyzed [4+2]‐Cycloaddition Reactions: A Sexennial Update
inferred← citeshttps://doi.org/10.1002/slct.202403149openalex-snapshot
Design, Synthesis, Anticancer Evaluation and Molecular Docking Study of Novel 4 H ‐Chromene‐7‐Azaindole‐1,2,3‐Triazole Hybrids
inferred← citeshttps://doi.org/10.1002/slct.202506700openalex-snapshot
Synthesis, Structural Characterization, and Biological Activities of Novel 2‐((9‐Oxo‐9H‐xanthen‐3‐yl)oxy)acetohydrazide Derivatives
inferred← citeshttps://doi.org/10.1002/slct.202507465openalex-snapshot
Advances in Metal‐Catalyzed Buchwald–Hartwig Coupling for Bioactive Molecule Synthesis: A Review
inferred← citeshttps://doi.org/10.1002/vjch.202000070openalex-snapshot
A new xanthone from the lichen Parmotrema praesorediosum (Parmeliaceae)
inferred← citeshttps://doi.org/10.1007/978-3-030-30746-2_9openalex-snapshot
Fungal Polyketides: Chemical Diversity and Their Cytotoxic Effects
inferred← citeshttps://doi.org/10.1007/978-3-642-38076-1_8openalex-snapshot
Antifungal Metabolites of Endophytic Fungi
inferred← citeshttps://doi.org/10.1007/s00044-020-02544-1openalex-snapshot
Oxygenated xanthones as P-glycoprotein modulators at the intestinal barrier: in vitro and docking studies
inferred← citeshttps://doi.org/10.1007/s00204-014-1193-yopenalex-snapshot
Induction and activation of P-glycoprotein by dihydroxylated xanthones protect against the cytotoxicity of the P-glycoprotein substrate paraquat
inferred← citeshttps://doi.org/10.1007/s00214-018-2294-0openalex-snapshot
The role of chlorine substituents in lichexanthones properties: the ionic and halogen bond interactions
inferred← citeshttps://doi.org/10.1007/s00299-016-1934-xopenalex-snapshot
Acetic acid acts as an elicitor exerting a chitosan-like effect on xanthone biosynthesis in Hypericum perforatum L. root cultures
inferred← citeshttps://doi.org/10.1007/s00299-018-2317-2openalex-snapshot
Chitosan oligosaccharides affect xanthone and VOC biosynthesis in Hypericum perforatum root cultures and enhance the antifungal activity of root extracts
inferred← citeshttps://doi.org/10.1007/s10600-015-1314-8openalex-snapshot
Xanthones from the Fermentation Products of the Endophytic Fungus of Phomopsis amygdali
inferred← citeshttps://doi.org/10.1007/s10600-015-1429-yopenalex-snapshot
Two New Flavones from Hypericum chinense and Their Anti-Tobacco Mosaic Virus Activity
inferred← citeshttps://doi.org/10.1007/s10600-019-02888-0openalex-snapshot
Two New Xanthones from Comastoma pulmonarium and Their Anti-Tobacco Mosaic Virus Activity
inferred← citeshttps://doi.org/10.1007/s10600-020-02991-7openalex-snapshot
Two New Anti-Tobacco Mosaic Virus Xanthones from Comastoma Pedunculatum
inferred← citeshttps://doi.org/10.1007/s11101-018-9577-xopenalex-snapshot
Have lichenized fungi delivered promising anticancer small molecules?
inferred← citeshttps://doi.org/10.1007/s11418-023-01681-2openalex-snapshot
Eumitrins I–K: three new xanthone dimers from the lichen Usnea baileyi
inferred← citeshttps://doi.org/10.1007/s13225-014-0288-3openalex-snapshot
Chemistry and biology of Pestalotiopsis-derived natural products
inferred← citeshttps://doi.org/10.1007/s13659-021-00317-wopenalex-snapshot
Natural Products as Potential Lead Compounds for Drug Discovery Against SARS-CoV-2
inferred← citeshttps://doi.org/10.1007/s42995-023-00170-5openalex-snapshot
Polyketides with potential bioactivities from the mangrove-derived fungus Talaromyces sp. WHUF0362
inferred← citeshttps://doi.org/10.1016/b978-0-08-099406-2.00016-9openalex-snapshot
Six-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-08-100017-5.00015-7openalex-snapshot
Six-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-405927-6.00011-4openalex-snapshot
Xanthones and Anthranoids from the Medicinal Plants of Africa
inferred← citeshttps://doi.org/10.1016/b978-0-12-816455-6.00003-2openalex-snapshot
Analysis of polyphenolics
inferred← citeshttps://doi.org/10.1016/b978-0-12-816675-8.00003-8openalex-snapshot
Bioactive C-glycosides inspired from natural products towards therapeutics
inferred← citeshttps://doi.org/10.1016/b978-0-443-15269-6.00006-7openalex-snapshot
Semisynthesis of natural products at room temperature
inferred← citeshttps://doi.org/10.1016/b978-0-443-30170-4.00010-3openalex-snapshot
Xanthones identified in the medicinal plants of Africa
inferred← citeshttps://doi.org/10.1016/bs.abr.2024.02.003openalex-snapshot
Pharmaceutical xanthones from African medicinal plants to fight cancers and their recalcitrant phenotypes
inferred← citeshttps://doi.org/10.1016/bs.aihch.2015.04.002openalex-snapshot
The Literature of Heterocyclic Chemistry, Part XIII, 2012–2013
inferred← citeshttps://doi.org/10.1016/j.bcab.2022.102471openalex-snapshot
Trapezifolixanthone as a common constituent in the genus Calophyllum: An insight Review
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108310openalex-snapshot
Structurally diverse tetrahydroxanthone analogues from Paraconiothyrium sp. AC31 with pyroptosis induction through targeted inhibition of PARP1 in hepatocellular carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109160openalex-snapshot
Structure, activity and biosynthesis of xanthones in genus Swertia
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.11.059openalex-snapshot
α-Pyrone derivatives, tetra/hexahydroxanthones, and cyclodepsipeptides from two freshwater fungi
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.04.017openalex-snapshot
Syntheses of benzophenone-xanthone hybrid polyketides and their antibacterial activities
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.06.079openalex-snapshot
α-Pyrone derivatives with cytotoxic activities, from the endophytic fungus Phoma sp. YN02-P-3
inferred← citeshttps://doi.org/10.1016/j.bmcl.2025.130154openalex-snapshot
Design, synthesis and biological evaluation of sulfur-containing tetrahydroxanthones as potential anti-tumor agents
inferred← citeshttps://doi.org/10.1016/j.bpc.2016.10.007openalex-snapshot
Assessing gastric toxicity of xanthone derivatives of anti-inflammatory activity using simulation and experimental approaches
inferred← citeshttps://doi.org/10.1016/j.catcom.2017.12.006openalex-snapshot
Nitric acid-catalyzed aerobic oxidation of benzylic sp3 C H bonds of isochromans, xanthenes and 9-fluorenone under additive-free conditions
inferred← citeshttps://doi.org/10.1016/j.cclet.2017.11.046openalex-snapshot
Concise synthesis of xanthones by the tandem etherification—Acylation of diaryliodonium salts with salicylates
inferred← citeshttps://doi.org/10.1016/j.cclet.2019.06.015openalex-snapshot
Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole/benzofuran-chromanone]s through organocatalytic inter-/intramolecular Michael cycloaddition
inferred← citeshttps://doi.org/10.1016/j.cclet.2024.110377openalex-snapshot
Asymmetric conjugated addition of aryl Grignard reagents for the construction of chromanones bearing quaternary stereogenic centers in batch and flow
inferred← citeshttps://doi.org/10.1016/j.chembiol.2016.03.013openalex-snapshot
A Multifunctional Monooxygenase XanO4 Catalyzes Xanthone Formation in Xantholipin Biosynthesis via a Cryptic Demethoxylation
inferred← citeshttps://doi.org/10.1016/j.chphi.2023.100411openalex-snapshot
Synthetic dimethoxyxanthones bind similarly to human serum albumin compared with highly oxygenated xanthones
inferred← citeshttps://doi.org/10.1016/j.cplett.2024.141834openalex-snapshot
Using proton abstraction as a nonlinear optical amplifier in xanthone-based molecules: A DFT perspective
inferred← citeshttps://doi.org/10.1016/j.culher.2018.05.013openalex-snapshot
Stains versus colourants produced by fungi colonising paper cultural heritage: A review
inferred← citeshttps://doi.org/10.1016/j.dscb.2025.100256openalex-snapshot
A concise review of synthetic xanthone derivatives for Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110106openalex-snapshot
Combining cycloaddition reactions for the one-pot synthesis of novel xanthoquinone dyes
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2022.100030openalex-snapshot
Synthesis, anticancer activities and experimental-theoretical DNA interaction studies of 2-amino-4-phenyl-4H-benzo[h]chromene-3-carbonitrile
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.09.012openalex-snapshot
Pyranoxanthones: Synthesis, growth inhibitory activity on human tumor cell lines and determination of their lipophilicity in two membrane models
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.07.073openalex-snapshot
A comprehensive review on xanthone derivatives as α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.028openalex-snapshot
All that glitters is not gold: Panning cytotoxic natural products and derivatives with a fused tricyclic backbone by the estimation of their leadlikeness for cancer treatment
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.07.039openalex-snapshot
Xanthone derivatives from the leaves of Garcinia oligantha
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115330openalex-snapshot
Anti-Vibrio potential of natural products from marine microorganisms
inferred← citeshttps://doi.org/10.1016/j.fgb.2020.103481openalex-snapshot
Identification of the polyketide synthase PKS7 responsible for the production of lecanoric acid and ethyl lecanorate in Claviceps purpurea
inferred← citeshttps://doi.org/10.1016/j.fitote.2013.09.004openalex-snapshot
Xanthone derivatives from the fermentation products of an endophytic fungus Phomopsis sp.
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.08.030openalex-snapshot
Polyketide derivatives from the sponge associated fungus Aspergillus europaeus with antioxidant and NO inhibitory activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.11.004openalex-snapshot
Xanthone-derived polyketides from the Thai mangrove endophytic fungus Phomopsis sp. xy21
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104194openalex-snapshot
Dimeric tetrahydroxanthones from the lichen Usnea aciculifera
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104449openalex-snapshot
Eumitrins C-E: Structurally diverse xanthone dimers from the vietnamese lichen Usnea baileyi
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104606openalex-snapshot
Chromanones and aryl glucoside analogs from the entomopathogenic fungus Aschersonia confluens BCC53152
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.147020openalex-snapshot
Studies on the toxic effects of three regioisomeric methoxylated xanthones against Trypanosoma cruzi amastigotes and their binding with human serum albumin
inferred← citeshttps://doi.org/10.1016/j.intimp.2019.106061openalex-snapshot
Xanthone suppresses allergic contact dermatitis in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.jchromb.2017.10.018openalex-snapshot
Lipophilicity assessement in drug discovery: Experimental and theoretical methods applied to xanthone derivatives
inferred← citeshttps://doi.org/10.1016/j.jlumin.2018.02.044openalex-snapshot
Fluorescence quenching of 2,7-diaminoxanthone in alcohols by hydrogen bonding: An experimental and theoretical research
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127305openalex-snapshot
Mechanistic density functional theory study of the Claisen Rearrangement Diels-Alder Cycloaddition domino sequence for the synthesis of the caged garcinia xanthone
inferred← citeshttps://doi.org/10.1016/j.orggeochem.2013.11.001openalex-snapshot
Contrasting diagenetic pathways of higher plant triterpenoids in buried wood as a function of tree species
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2014.11.013openalex-snapshot
Modulation of P-glycoprotein efflux pump: induction and activation as a therapeutic strategy
inferred← citeshttps://doi.org/10.1016/j.phymed.2016.02.012openalex-snapshot
Secondary metabolites from cetrarioid lichens: Chemotaxonomy, biological activities and pharmaceutical potential
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112329openalex-snapshot
Cytotoxic xanthone derivatives from the twigs of Garcinia oligantha
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109524openalex-snapshot
Systematic molecular dissection of key intermediates in xanthones biosynthesis in Cudrania tricuspidata and establishment of a viable heterologous expression system
inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103421openalex-snapshot
Synthesis and characterization of novel xanthones appended with 1,2,3–triazoles: antimicrobial screening, in silico docking and ADMET predictions
inferred← citeshttps://doi.org/10.1016/j.sajb.2023.08.021openalex-snapshot
Chemistry and biological activities of naturally occurring C-glycosylxanthones
inferred← citeshttps://doi.org/10.1016/j.synbio.2022.03.007openalex-snapshot
Structure-based identification and pathway elucidation of flavonoids in Camptotheca acuminate
inferred← citeshttps://doi.org/10.1016/j.tet.2013.12.055openalex-snapshot
Synthesis of toxyloxanthone B
inferred← citeshttps://doi.org/10.1016/j.tet.2018.04.003openalex-snapshot
Expedient synthesis of xanthones and multi-functionalized chromones from 1,1-diacyl cyclopropanes
inferred← citeshttps://doi.org/10.1016/j.tet.2018.05.052openalex-snapshot
Highly efficient construction of chiral dispirocyclic oxindole/thiobutyrolactam/chromanone complexes through Michael/cyclization cascade reactions with a rosin-based squaramide catalyst
inferred← citeshttps://doi.org/10.1016/j.tet.2018.08.007openalex-snapshot
A novel entry to xanthones by an intramolecular Diels-Alder reaction involving 2-(1,2-dichlorovinyloxy) aryl dienones
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130646openalex-snapshot
Benzophenone and chromone derivatives and their dimers from the scale-insect pathogenic fungus Orbiocrella petchii BCC 51377
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132501openalex-snapshot
Recent total syntheses of anthraquinone-based natural products
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.03.129openalex-snapshot
Semi-synthesis of neomangiferin from mangiferin
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.08.062openalex-snapshot
[RuCl2(p-cymene)2]2 catalyzed cross dehydrogenative coupling (CDC) toward xanthone and fluorenone analogs through intramolecular C–H bond functionalization reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.08.121openalex-snapshot
Indirect electrochemical oxidation of substituted polycyclic aromatic hydrocarbons to corresponding para-quinones with potassium bromide in water–chloroform medium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.11.032openalex-snapshot
Regioselective synthesis of multiply halogenated azaxanthones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.12.111openalex-snapshot
Asperdichrome, an unusual dimer of tetrahydroxanthone through an ether bond, with protein tyrosine phosphatase 1B inhibitory activity, from the Okinawan freshwater Aspergillus sp. TPU1343
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.10.038openalex-snapshot
Total synthesis of (+)-blennolide C and (+)-gonytolide C via spirochromanone
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.04.010openalex-snapshot
Kinetics improvement of protease-mediated formation of pyronin dyes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.04.034openalex-snapshot
Proangiogenic penibishexahydroxanthone A from the marine-derived fungus Penicillium sp. ZZ486A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154871openalex-snapshot
Total synthesis of natural products containing bicyclo[n.2.2] ring systems
inferred← citeshttps://doi.org/10.1016/j.toxrep.2021.04.013openalex-snapshot
Aspergillus derived mycotoxins in food and the environment: Prevalence, detection, and toxicity
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c04265openalex-snapshot
Herbicidal and Antifungal Xanthone Derivatives from the Alga-Derived Fungus Aspergillus versicolor D5
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c03513openalex-snapshot
New Xanthones with Antiagricultural Fungal Pathogen Activities from the Endophytic Fungus Diaporthe goulteri L17
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c00757openalex-snapshot
Small Molecular Mimetics of Antimicrobial Peptides as a Promising Therapy To Combat Bacterial Resistance
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.6b01403openalex-snapshot
Symmetrically Substituted Xanthone Amphiphiles Combat Gram-Positive Bacterial Resistance with Enhanced Membrane Selectivity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00523openalex-snapshot
Cytotoxic Xanthone Derivatives from the Mangrove-Derived Endophytic Fungus Peniophora incarnata Z4
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00535openalex-snapshot
Staprexanthones, Xanthone-Type Stimulators of Pancreatic β-Cell Proliferation from a Mangrove Endophytic Fungus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01212openalex-snapshot
Bioactive Dimeric Tetrahydroxanthones with 2,2′- and 4,4′-Axial Linkages from the Entomopathogenic Fungus Aschersonia confluens
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00022openalex-snapshot
Heterologous Biosynthesis of Tetrahydroxanthone Dimers: Determination of Key Factors for Selective or Divergent Synthesis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00264openalex-snapshot
Insights into Ergochromes of the Plant Pathogen Claviceps purpurea
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00878openalex-snapshot
Anti-inflammatory Dimeric Tetrahydroxanthones from an Endophytic Muyocopron laterale
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00353openalex-snapshot
Cladoxanthones A and B, Xanthone-Derived Metabolites with a Spiro[cyclopentane-1,2′-[3,9a]ethanoxanthene]-2,4′,9′,11′-tetraone Skeleton from a Cladosporium sp.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00628openalex-snapshot
Subplenones A–J: Dimeric Xanthones with Antibacterial Activity from the Endophytic Fungus Subplenodomus sp. CPCC 401465
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00239openalex-snapshot
Polycyclic Polyprenylated Xanthones from Symphonia globulifera: Isolation and Biomimetic Electrosynthesis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00636openalex-snapshot
Versixanthones A–F, Cytotoxic Xanthone–Chromanone Dimers from the Marine-Derived Fungus Aspergillus versicolor HDN1009
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00376openalex-snapshot
Isolation and Identification of Xanthone, Benzofuran, and Spirolactone Derivatives from Dinemasporium parastrigosum KT4144 and Their Plausible Biosynthetic Pathways
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00251openalex-snapshot
Polyprenylated Tetraoxygenated Xanthones from the Roots ofHypericum monogynumand Their Neuroprotective Activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00417openalex-snapshot
Regiospecific Prenylation of Hydroxyxanthones by a Plant Flavonoid Prenyltransferase
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01071openalex-snapshot
Bioactive Polyhydroxanthones from Penicillium purpurogenum
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00528openalex-snapshot
Total Synthesis of Chalaniline B: An Antibiotic Aminoxanthone from Vorinostat-Treated Fungus Chalara sp. 6661
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02997openalex-snapshot
Flexible Approach for the Synthesis of Annulated 4H-Pyrans Based on a Cu(I)-Catalyzed C-Allylation/O-Vinylation Reaction of Cyclic 1-Bromoallyl Tosylates with Cyclic and Acyclic 1,3-Dicarbonyls
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00683openalex-snapshot
Visible Light-Driven Reductive Azaarylation of Coumarin-3-carboxylic Acids
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