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Three New Resveratrol Oligomers from the Stem Bark of Vatica p auciflora
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0031-9422(82)85262-xopenalex-snapshot
Polyphenols from Stemonoporus species
inferredcites →https://doi.org/10.1016/s0031-9422(00)00026-1openalex-snapshot
Oligostilbenoids in stem bark of Vatica rassak
inferredcites →https://doi.org/10.1016/s0031-9422(00)81845-2openalex-snapshot
Further evidence for the structure of vaticaffinol and a revision of its stereochemistry
inferredcites →https://doi.org/10.1016/s0031-9422(00)95070-2openalex-snapshot
Distribution of resveratrol oligomers in plants
inferredcites →https://doi.org/10.1248/cpb.46.663openalex-snapshot
Phenolic Compounds Isolated from the Roots of Sophora stenophylla.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Stilbenes: Source plants, chemistry, biosynthesis, pharmacology, application and problems related to their clinical Application-A comprehensive review
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inferred← citeshttps://doi.org/10.1002/anie.201107730openalex-snapshot
Total Syntheses of Hopeanol and Hopeahainol A Empowered by a Chiral Brønsted Acid Induced Pinacol Rearrangement
inferred← citeshttps://doi.org/10.1002/anie.201813071openalex-snapshot
Pd‐Catalyzed Enantioselective Ring Opening/Cross‐Coupling and Cyclopropanation of Cyclobutanones
inferred← citeshttps://doi.org/10.1002/anie.201813699openalex-snapshot
Palladium/Norbornene‐Catalyzed Indenone Synthesis from Simple Aryl Iodides: Concise Syntheses of Pauciflorol F and Acredinone A
inferred← citeshttps://doi.org/10.1002/anie.202013792openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202103465openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202317433openalex-snapshot
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Nickel‐Catalyzed Ring Expansion of Cyclobutanones towards Indanones
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inferred← citeshttps://doi.org/10.1016/j.fbio.2021.101004openalex-snapshot
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Nickel-Catalyzed Asymmetric Domino Ring Opening/Cross-Coupling Reaction of Cyclobutanones via a Reductive Strategy
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inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02130openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.3c01986openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jm300390fopenalex-snapshot
6-(Methylamino)hexane-1,2,3,4,5-pentanol 4-(((1S,2S)-1-Hydroxy-2,3-dihydro-1H,1′H-[2,2-biinden]-2-yl)methyl)benzoate (PH46A): A Novel Small Molecule With Efficacy In Murine Models Of Colitis
inferred← citeshttps://doi.org/10.1021/jo102298popenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo2009164openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np1002675openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol102756mopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol401752uopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol402980vopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol902141zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c4ob02103gopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c4ra03371jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c4ra04763jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c5cc03040dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c5ob00859jopenalex-snapshot
Enantioselective N-heterocyclic carbene-catalyzed synthesis of indenopyrones
inferred← citeshttps://doi.org/10.1039/c5ra12234aopenalex-snapshot
Superacid mediated intramolecular condensation: facile synthesis of indenones and indanones
inferred← citeshttps://doi.org/10.1039/c6cc08032dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c6ra16462eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c8ra07325bopenalex-snapshot
Applications of Friedel–Crafts reactions in total synthesis of natural products
inferred← citeshttps://doi.org/10.1039/c9qo00765bopenalex-snapshot
Diastereoselective access to 2-aminoindanones via the rhodium( ii )-catalyzed tandem reaction involving O–H insertion and Michael addition
inferred← citeshttps://doi.org/10.1039/c9sc02431jopenalex-snapshot
Enantioselective palladium/copper-catalyzed C–C σ-bond activation synergized with Sonogashira-type C(sp 3 )–C(sp) cross-coupling alkynylation
inferred← citeshttps://doi.org/10.1039/d0gc00771dopenalex-snapshot
Electrocatalytic three-component annulation-halosulfonylation of 1,6-enynes toward 1-indanones using sodium halides as both halogen sources and electrolytes
inferred← citeshttps://doi.org/10.1039/d0gc03572fopenalex-snapshot
A metal-free method for the facile synthesis of indanones via the intramolecular hydroacylation of 2-vinylbenzaldehyde
inferred← citeshttps://doi.org/10.1039/d0np00005aopenalex-snapshot
An invocation for computational evaluation of isomerization transforms: cationic skeletal reorganizations as a case study
inferred← citeshttps://doi.org/10.1039/d0np00030bopenalex-snapshot
Phytostilbenes as agrochemicals: biosynthesis, bioactivity, metabolic engineering and biotechnology
inferred← citeshttps://doi.org/10.1039/d1cc02973hopenalex-snapshot
Copper/silver co -mediated three-component bicyclization for accessing indeno[1,2- c ]azepine-3,6-diones
inferred← citeshttps://doi.org/10.1039/d1cc04167copenalex-snapshot
Cu-catalyzed coupling of indanone oxime acetates with thiols to 2,3-difunctionalized indenones
inferred← citeshttps://doi.org/10.1039/d1cc05286aopenalex-snapshot
Palladium-catalysed alkenyl and carbonylative C–C bond activation of cyclobutanones
inferred← citeshttps://doi.org/10.1039/d1ob00071copenalex-snapshot
Synthesis of methanesulfone-containing tetrasubstituted carbon stereocenters
inferred← citeshttps://doi.org/10.1039/d1qo00467kopenalex-snapshot
Palladium-catalyzed gaseous CO-free carbonylative C–C bond activation of cyclobutanones
inferred← citeshttps://doi.org/10.1039/d1qo00487eopenalex-snapshot
Regioselective synthesis of indenones via nickel-catalyzed Larock annulations
inferred← citeshttps://doi.org/10.1039/d2cc00149gopenalex-snapshot
Merging C–C σ-bond activation of cyclobutanones with CO 2 fixation via Ni-catalysis
inferred← citeshttps://doi.org/10.1039/d2cc01324jopenalex-snapshot
Transition-metal-free approaches to 2,3-diarylated indenones from 2-alkynylbenzaldehydes and phenols with tunable selectivity
inferred← citeshttps://doi.org/10.1039/d2ob00595fopenalex-snapshot
Solvent controlled synthesis of 2,3-diarylepoxy indenones and α-hydroxy diarylindanones and their evaluation as inhibitors of DNA alkylation repair
inferred← citeshttps://doi.org/10.1039/d3ob01787gopenalex-snapshot
Synthesis of 2-amidoindenone derivatives through an ynamide carbosilylation/Houben–Hoesch cyclization 2-step sequence
inferred← citeshttps://doi.org/10.1039/d3qo01790gopenalex-snapshot
Annulation of benzaldehydes with norbornenes toward indanones assisted by monodentate transient directing groups via double C–H activation
inferred← citeshttps://doi.org/10.1039/d4ob01810aopenalex-snapshot
Metal-free radical cascade cyclization/haloazidation of enynones to access functionalized 1-indanones
inferred← citeshttps://doi.org/10.1039/d5ra05436bopenalex-snapshot
Synthesis of indenones via photo-induced radical cascade cyclization of alkynes with alkyl halides
inferred← citeshttps://doi.org/10.1039/d6cc03320bopenalex-snapshot
Visible-light-induced synthesis of indanones via the annulation of α-hydroxy ketones and alkynes
inferred← citeshttps://doi.org/10.1055/a-2924-5139openalex-snapshot
Transition-Metal-Catalyzed C–H Activation-Enabled [3+2] Annulations for the Synthesis of Functionalized Indanones
inferred← citeshttps://doi.org/10.1080/00397911.2013.820835openalex-snapshot
Advances in the First Total Synthesis of Natural Flavonoids
inferred← citeshttps://doi.org/10.1080/00397911.2017.1303510openalex-snapshot
Synthetic strategies toward the synthesis of polyphenolic natural products: Pauciflorol F and isopaucifloral F: A review
inferred← citeshttps://doi.org/10.1088/1742-6596/423/1/012045openalex-snapshot
Oligostilbenoids from Vatica pauciflora and the Oxidative Effect on Chang Cells
inferred← citeshttps://doi.org/10.1107/s1600536813018990openalex-snapshot
2-(Diphenylmethylidene)-2,3-dihydro-1H-inden-1-one
inferred← citeshttps://doi.org/10.11113/jt.v77.5989openalex-snapshot
MONOMER STILBENOID GLUCOSIDES FROM Vatica pauciflora AND Vatica lowii (DIPTEROCARPACEAE)
inferred← citeshttps://doi.org/10.1246/cl.200837openalex-snapshot
Flash Chemistry Makes Impossible Organolithium Chemistry Possible
inferred← citeshttps://doi.org/10.1248/cpb.55.1535openalex-snapshot
Resveratrol Tetramers with a C6-C3 or a C1 Unit from Upuna borneensis
inferred← citeshttps://doi.org/10.1248/cpb.59.452openalex-snapshot
Resveratrol Derivatives from Vatica albiramis
inferred← citeshttps://doi.org/10.1248/yakushi.131.93openalex-snapshot
Structures of Oligostilbenoids in Dipterocarpaceaeous Plants and Their Biological Activities
inferred← citeshttps://doi.org/10.12720/jolst.1.4.205-209openalex-snapshot
Antioxidant Properties of Vatica pauciflora and Vatica lowii Crude Extracts
inferred← citeshttps://doi.org/10.2174/0118756298307930240531072440openalex-snapshot
A Comprehensive Review on History, Sources, Biosynthesis, Chemical Synthesis and Applications of Stilbenes
inferred← citeshttps://doi.org/10.3389/fchem.2020.00234openalex-snapshot
Copper-Catalyzed Annulation–Cyanotrifluoromethylation of 1,6-Enynes Toward 1-Indanones via a Radical Process
inferred← citeshttps://doi.org/10.3390/md21120640openalex-snapshot
Streptinone, a New Indanone Derivative from a Marine-Derived Streptomyces massiliensis, Inhibits Particulate Matter-Induced Inflammation
inferred← citeshttps://doi.org/10.3390/molecules22122050openalex-snapshot
Update on Phytochemistry and Pharmacology of Naturally Occurring Resveratrol Oligomers
inferred← citeshttps://doi.org/10.3390/molecules30143019openalex-snapshot
Advances in α-Arylation of Carbonyl Compounds: Diaryliodonium Salts as Arylating Agents
inferred← citeshttps://doi.org/10.3987/com-10-12116openalex-snapshot
Resveratrol Dimers with an Oxabicyclo Ring in Vatica albiramis
inferred← citeshttps://doi.org/10.6023/cjoc202106014openalex-snapshot
Visible-Light-Driven Photocatalytic Kharasch-Type Addition of 1,6-Enynes
inferred← citeshttps://doi.org/10.70675/0530eba3z4f4fz4ad3z889bz0213651d162eopenalex-snapshot
Synthèse et application de synthons originaux de type 2-aminoacrylonitriles
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