On the public citation graph

Nitrogen-Containing Compounds from Salvia m iltiorrhiza

0 signed · 167 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf02541500openalex-snapshot
The structure of rosmariquinone — A new antioxidant isolated fromRosmarinus officinalis L.
inferredcites →https://doi.org/10.1007/bf02541501openalex-snapshot
Comparative studies of three solvent mixtures for the extraction of soybean lipids
inferredcites →https://doi.org/10.1016/0223-5234(87)90305-9openalex-snapshot
Pharmacology and applications of chinese materia medica
inferredcites →https://doi.org/10.1016/s0367-326x(01)00344-6openalex-snapshot
A new pyrrole alkaloid from seeds of Castanea sativa
inferredcites →https://doi.org/10.1021/jo00131a006openalex-snapshot
Aromatic Annulation Strategy for the Synthesis of Angularly-Fused Diterpenoid Quinones. Total Synthesis of (+)-Neocryptotanshinone, (-)-Cryptotanshinone, Tanshinone IIA, and (.+-.)-Royleanone
inferredcites →https://doi.org/10.1248/cpb.31.1670openalex-snapshot
New platelet aggregation inhibitors from Tan-Shen; Radix of Salvia miltiorrhiza Bunge.
inferredcites →https://doi.org/10.1248/yakushi.123.517openalex-snapshot
Anti-inflammatory Constituents, Aloesin and Aloemannan in Aloe Species and Effects of Tanshinon VI in Salvia miltiorrhiza on Heart

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4640447openalex-extracted
Gold Nanoparticles-Decorated Carbon Materials for Highly Efficient Cyclization of 2-Aminophenol/2-Aminothiophenol with Aromatic Aldehydes
inferred← citeshttps://doi.org/10.1002/9781118939901.ch5openalex-snapshot
Beckmann Rearrangements and Fragmentations in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/adsc.201500515openalex-snapshot
Copper‐Catalyzed Aerobic Oxidative C(aryl)OH Bond Functionalization of Catechols with Amines Affording Benzoxazoles
inferred← citeshttps://doi.org/10.1002/adsc.201901096openalex-snapshot
Amino Acids: Nontoxic and Cheap Alternatives for Amines for the Synthesis of Benzoxazoles through the Oxidative Functionalization of Catechols
inferred← citeshttps://doi.org/10.1002/adsc.202100249openalex-snapshot
Metal‐Free Oxidative Condensation of Catechols, Aldehydes and NH4OAc towards Benzoxazoles
inferred← citeshttps://doi.org/10.1002/ajoc.201600131openalex-snapshot
Copper‐Catalyzed C−H Oxygenation of Benzoxepine‐4‐carboxylates: Facile Synthesis and Photophysical Properties of Naphtho[2,1‐d]oxazoles and Benzo[c]phenoxazines
inferred← citeshttps://doi.org/10.1002/ajoc.201700147openalex-snapshot
Diphenylphosphoryl Azide (DPPA)‐Mediated One‐Pot Synthesis of Oxazolo[4,5‐c][1,8]naphthyridin‐4(5 H)‐ones, Oxazolo[4,5‐c]quinoline‐4(5 H)‐ones, and Tosyloxazol‐5‐yl Pyridines
inferred← citeshttps://doi.org/10.1002/ajoc.202100043openalex-snapshot
Intermolecular Amination of Ketoximes with Anthranils by Rh‐Catalyzed C−H Bond Activation in Air
inferred← citeshttps://doi.org/10.1002/ange.201915685openalex-snapshot
The Biosynthesis of the Benzoxazole in Nataxazole Proceeds via an Unstable Ester and has Synthetic Utility
inferred← citeshttps://doi.org/10.1002/anie.201915685openalex-snapshot
The Biosynthesis of the Benzoxazole in Nataxazole Proceeds via an Unstable Ester and has Synthetic Utility
inferred← citeshttps://doi.org/10.1002/aoc.4240openalex-snapshot
Palladium(II) Immobilized Onto the Glucose Functionalized Magnetic Nanoparticle as a New and Efficient Catalyst for the One‐pot Synthesis of Benzoxazoles
inferred← citeshttps://doi.org/10.1002/aoc.6330openalex-snapshot
Synthesis of novel benzimidazoles and benzothiazoles via furan‐2‐carboxaldehydes, o‐phenylenediamines, and 2‐aminothiophenol using Cu(II) Schiff‐base@SiO2 as a nanocatalyst
inferred← citeshttps://doi.org/10.1002/aoc.70276openalex-snapshot
New Dihydroxyacetophenone‐Based Vanadyl(IV) Complex Anchored to Fe 3 O 4 as a Catalyst for Benzoxazole Production: Investigating the Kinetic Parameters
inferred← citeshttps://doi.org/10.1002/asia.202201151openalex-snapshot
Synthesis of tetracyclic 4H‐benzo[5,6]chromeno[3,4‐d]oxazoles via palladium‐catalyzed intramolecular direct heteroarylation
inferred← citeshttps://doi.org/10.1002/asia.202400116openalex-snapshot
Progress in Electrochemically Empowered C−O Bond Formation: Unveiling the Pathway of Efficient Green Synthesis
inferred← citeshttps://doi.org/10.1002/cbdv.201200418openalex-snapshot
Phytochemical Investigation of Annulohypoxylon ilanense, an Endophytic Fungus Derived from Cinnamomum Species
inferred← citeshttps://doi.org/10.1002/chem.201503791openalex-snapshot
Relayed Regioselective Alkynylation/Olefination of Unsymmetrical Cyclic Diaryliodonium Species Catalyzed by Cu and Pd: Affording Fluorescent Cytotoxic Benzoxazoles
inferred← citeshttps://doi.org/10.1002/ejoc.201900699openalex-snapshot
A Gold‐Catalyzed Acid‐Assisted Regioselective Cyclization for the Synthesis of Polysubstituted Oxazoles
inferred← citeshttps://doi.org/10.1002/ejoc.202000999openalex-snapshot
Consecutive Oxidation/Condensation/Cyclization/Aromatization Sequences Catalyzed by Nanostructured Iron(III)‐Porphyrin Complex towards Benzoxazole Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202100942openalex-snapshot
C–H Amination Enabled [2+1+1+1] Annulation Reaction in Water: Access to Benzoxazoles
inferred← citeshttps://doi.org/10.1002/ejoc.202500293openalex-snapshot
Hypodiboric Acid–Sodium Carbonate Mediated Reductive Cyclization of Nitro(Hetero)Arenes: Synthesis of Imidazopyridines, Benz(oxa/thia)zoles, Benzoxazolones, and Benzoxathiones
inferred← citeshttps://doi.org/10.1002/hlca.201200608openalex-snapshot
New Pyrrole Alkaloids with Bulky N‐Alkyl Side Chains Containing Stereogenic Centers from Lycium chinense
inferred← citeshttps://doi.org/10.1002/jccs.201800489openalex-snapshot
Biosynthesis of Fe 3 O 4 ‐magnetic nanoparticles using clover leaf aqueous extract: Green synthesis of 1,3‐benzoxazole derivatives
inferred← citeshttps://doi.org/10.1002/jhet.3992openalex-snapshot
Novel N‐(benzo[d]oxazol‐2‐yl)alkanamides; synthesis and carbonic anhydrase II inhibition studies
inferred← citeshttps://doi.org/10.1002/slct.201900550openalex-snapshot
Facile Preparation of Benzoxazoles from S 8 ‐Promoted Cyclization of 2‐Nitrophenols with Arylmethyl Chloride
inferred← citeshttps://doi.org/10.1002/slct.202200794openalex-snapshot
Immobilized Cu‐Schiff Base Complex on MCM‐41as Catalyst in the Synthesis of Benzimidazole Derivatives
inferred← citeshttps://doi.org/10.1002/vjch.202200019openalex-snapshot
Constituents of Vernonia gratiosa Hance and their α‐glucosidase and xanthine oxidase inhibitory activities
inferred← citeshttps://doi.org/10.1007/978-3-030-24716-4_1openalex-snapshot
Salvia miltiorrhiza: An Economically and Academically Important Medicinal Plant
inferred← citeshttps://doi.org/10.1007/978-81-322-2163-0_4openalex-snapshot
Natural Sources of Anti-inflammation
inferred← citeshttps://doi.org/10.1007/978-94-017-9463-3_3openalex-snapshot
Active Constituents in Danshen and Their Pharmacological Actions
inferred← citeshttps://doi.org/10.1007/s00706-016-1685-yopenalex-snapshot
Synthesis and biological evaluation of benzoxazole fused combretastatin derivatives as anticancer agents
inferred← citeshttps://doi.org/10.1007/s10600-015-1327-3openalex-snapshot
A New Pyrrole Metabolite from the Endophytic Fungus of Xylaria papulis
inferred← citeshttps://doi.org/10.1007/s10600-017-2048-6openalex-snapshot
Chemical Constituents of Capparis spinosa
inferred← citeshttps://doi.org/10.1007/s11094-025-03350-yopenalex-snapshot
HPLC Determination of Salvianolic Acid B and Rosmarinic Acid from the Aerial Parts and Roots of Salvia miltiorrhiza Bge.
inferred← citeshttps://doi.org/10.1007/s11101-015-9427-zopenalex-snapshot
Bioactive phytochemicals from shoots and roots of Salvia species
inferred← citeshttps://doi.org/10.1007/s11164-024-05230-8openalex-snapshot
Synthesis, insecticidal activity, and in silico study of novel carboxamide compounds containing benzoxazole moiety
inferred← citeshttps://doi.org/10.1007/s12039-013-0544-1openalex-snapshot
Application of nano SnO2 as a green and recyclable catalyst for the synthesis of 2-aryl or alkylbenzoxazole derivatives under ambient temperature
inferred← citeshttps://doi.org/10.1007/s13659-015-0080-4openalex-snapshot
Diterpenoids from the Roots of Salvia yunnanensis
inferred← citeshttps://doi.org/10.1007/s13659-025-00541-8openalex-snapshot
Neuroprotective effects of chemical constituents from Nicotiana tabacum L. in Parkinson’s disease
inferred← citeshttps://doi.org/10.1007/s13738-023-02949-wopenalex-snapshot
Structure determination and DFT studies of some organoplatinum(II) complexes containing 5,7-di-tert-butyl-2-(thiophen-2-yl)benzo[d]oxazole
inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00007-3openalex-snapshot
Five-Membered Ring Systems: Furans and Benzofurans
inferred← citeshttps://doi.org/10.1016/b978-0-323-85386-6.00001-9openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1016/bs.alkal.2017.12.002openalex-snapshot
Benzoxazole Alkaloids: Occurrence, Chemistry, and Biology
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.08.109openalex-snapshot
Hydrolytic instability of the important orexin 1 receptor antagonist SB-334867: Possible confounding effects on in vivo and in vitro studies
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.10.038openalex-snapshot
Facile synthesis of 2-aryl 5-hydroxy benzo[d]oxazoles and their in vitro anti-proliferative effects on various cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.bmcl.2025.130376openalex-snapshot
Design, Ssynthesis and Ddocking study of 1,2,3-triazole incorporated benzoxazole-oxazole derivatives and evaluation as potential anticancer agents
inferred← citeshttps://doi.org/10.1016/j.bse.2026.105343openalex-snapshot
Chemical constituents of Paratinospora sagittata and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.catcom.2017.01.005openalex-snapshot
Environmental benign synthesis of novel double layered nano catalyst and their catalytic activity in synthesis of 2-substituted benzoxazoles
inferred← citeshttps://doi.org/10.1016/j.crci.2016.12.008openalex-snapshot
TiO2ZrO2 composite: Synthesis, characterization and application as a facile, expeditious and recyclable catalyst for the synthesis of 2-aryl substituted benzoxazole derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.04.053openalex-snapshot
Synthesis, molecular structure, DNA-binding, cytotoxicity, apoptosis and antioxidant activity of compounds containing aryloxazole
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113708openalex-snapshot
Design, synthesis and biological evaluation of tanshinone IIA-based analogues: Potent inhibitors of microtubule formation and angiogenesis
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106392openalex-snapshot
Three new diterpenes from the roots of Salvia miltiorrhiza and their cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.ica.2019.119222openalex-snapshot
Synthesis and X-ray crystal structures of three new nickel(II) complexes of benzoylhydrazones: Catalytic applications in the synthesis of 2-arylbenzoxazoles
inferred← citeshttps://doi.org/10.1016/j.jep.2025.120032openalex-snapshot
Ethnomedicine, phytochemistry, pharmacology, pharmacokinetics, and clinical application of Salvia miltiorrhiza Bunge (Lamiaceae): A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2014.02.013openalex-snapshot
A novel and efficient route for the synthesis of 5-nitrobenzo[d]oxazole derivatives
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2021.121881openalex-snapshot
Iron(III)-catalyzed aerobic oxidation for the synthesis of 1-benzoxazolyl-o-carboranes
inferred← citeshttps://doi.org/10.1016/j.micromeso.2019.04.034openalex-snapshot
Palladium oxide nanoparticles intercalated mesoporous silica for solvent free acceptorless dehydrogenation reactions of alcohols
inferred← citeshttps://doi.org/10.1016/j.micromeso.2019.109922openalex-snapshot
Surface-driven imidazolium-coated periodic mesoporous organosilicas for selective synthesis of electron-deficient 2-arylbenzo[d]oxazoles
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.07.023openalex-snapshot
Vibrational spectroscopic investigations and molecular docking studies of biologically active 2-[4-(4-phenylbutanamido)phenyl]-5-ethylsulphonyl-benzoxazole
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127352openalex-snapshot
Quantum-chemical modeling, spectroscopic (FT-IR, excited states, UV/Vis, polarization, and Dichroism) studies of two new benzo[d]oxazole derivatives
inferred← citeshttps://doi.org/10.1016/j.phytochem.2005.12.009openalex-snapshot
Salvidorol, a nor-abietane diterpene with a rare carbon skeleton and two abietane diterpene derivatives from Salvia dorrii
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.07.001openalex-snapshot
Cytotoxic diterpenoids from Salvia yunnanensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113673openalex-snapshot
The tanshinones from the plant of Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114300openalex-snapshot
Anti-inflammatory oxazole-, nitro- and hexahydropyrrolo[2,1-b]oxazole-containing abietane diterpenoid alkaloids from Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.04.001openalex-snapshot
Chemical constituents from Laggera pterodonta and their anti-inflammatory activities in vitro
inferred← citeshttps://doi.org/10.1016/j.rechem.2025.102359openalex-snapshot
Design, synthesis and biological evaluation of aryl chalcone derivatives of pyridine-benzoxazole-pyimidine-oxazole as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.saa.2013.09.028openalex-snapshot
Synthesis, molecular structure, DNA interaction and antioxidant activity of novel naphthoxazole compound
inferred← citeshttps://doi.org/10.1016/j.synthmet.2024.117663openalex-snapshot
Gold-decorated carbon material for enhanced catalytic performance of cyclization/oxidation of 2-aminophenol, 2-aminothiophenol, and 2-aminoaniline with aromatic aldehydes
inferred← citeshttps://doi.org/10.1016/j.tet.2010.10.082openalex-snapshot
Unexpected reaction of 2-amino-1,4-naphthoquinone with aldehydes: new synthesis of naphtho[2,1-d]oxazole compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2011.04.107openalex-snapshot
An expedient synthesis of salviadione
inferred← citeshttps://doi.org/10.1016/j.tet.2012.11.021openalex-snapshot
Site-selective Suzuki–Miyaura reactions of 2,6-dichlorobenzoxazole
inferred← citeshttps://doi.org/10.1016/j.tet.2014.11.066openalex-snapshot
Hypervalent iodine-mediated synthesis of benzoxazoles and benzimidazoles via an oxidative rearrangement
inferred← citeshttps://doi.org/10.1016/j.tet.2019.01.044openalex-snapshot
Synthesis of C3-Symmetric star-shaped molecules containing 1,3-azoles via hetero-aryl Heck coupling
inferred← citeshttps://doi.org/10.1016/j.tet.2022.133057openalex-snapshot
I2-DMSO mediated N1/C5 difunctionalization of anthranils with aryl methyl ketones: A facile access to multicarbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135038openalex-snapshot
Construction of 2-naphtho[1,2-d][1,3]oxazoles via base-promoted reaction of 1-nitroso-2-naphthol with isothiocyanates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.03.027openalex-snapshot
An efficient potassium cyanide-promoted synthesis of 2-arylbenzoxazoles from [4.3.0]boron heterobicycles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.06.039openalex-snapshot
Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.01.015openalex-snapshot
Catalyst-free synthesis of coumarin-, quinolone- and pyridine-annulated oxazole derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.150openalex-snapshot
Intermolecular coupling of 2-iodoanilides with benzoxazoles: synthesis of N-(2-Benzoxazol-2-ylphenyl)benzamides via C–H activation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.10.078openalex-snapshot
Ligand-promoted, copper nanoparticles catalyzed one-pot synthesis of substituted benzoxazoles from 2-bromoanilines and acyl chlorides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.11.046openalex-snapshot
Design, synthesis and cytotoxicity of nitrogen-containing tanshinone derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.05.073openalex-snapshot
Semisynthesis of miltirone, 1,2-dehydromiltirone, saligerone from carnosic acid and cytotoxities of their derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.12.017openalex-snapshot
Organocatalytic oxidative synthesis of C2-functionalized benzoxazoles, naphthoxazoles, benzothiazoles and benzimidazoles
inferred← citeshttps://doi.org/10.1016/s0959-6380(07)80011-0openalex-snapshot
Five–membered ring systems: furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30010-xopenalex-snapshot
Danshen: a phytochemical and pharmacological overview
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00543openalex-snapshot
Wulfenioidins D–N, Structurally Diverse Diterpenoids with Anti-Zika Virus Activity Isolated from Orthosiphon wulfenioides
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00659openalex-snapshot
Oxazole-Containing Diterpenoids from Cell Cultures of Salvia miltiorrhiza and Their Anti-HIV-1 Activities
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00560openalex-snapshot
One-Pot Multicomponent Reaction of Catechols, Ammonium Acetate, and Aldehydes for the Synthesis of Benzoxazole Derivatives Using the Fe(III)–Salen Complex
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02329openalex-snapshot
Direct Synthesis of Fluorescent Oxazolo-phenoxazines by Copper-Catalyzed/Hypervalent Iodine(III)-Mediated Dimerization/Cyclization of 2-Benzylamino-phenols
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01919openalex-snapshot
Construction of Naphtho[2,1-d]oxazoles and 1,4-Epoxyisoquinolines via Regioselectivity-Switchable Diels–Alder Reaction of 4-Alkenyloxazoles with Arynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00784openalex-snapshot
Cyanide Boosting Copper Catalysis: A Mild Approach to Fluorescent Benzazole Derivatives from Nonemissive Schiff Bases in Biological Media
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01061openalex-snapshot
Selective Aerobic C–H Amination of Phenols with Primary Amines over Copper toward Benzoxazoles
inferred← citeshttps://doi.org/10.1021/acscombsci.9b00004openalex-snapshot
Synthesis of Benz-Fused Azoles via C-Heteroatom Coupling Reactions Catalyzed by Cu(I) in the Presence of Glycosyltriazole Ligands
inferred← citeshttps://doi.org/10.1021/acsomega.1c03207openalex-snapshot
One-Pot Multicomponent Coupling Reaction of Catechols, Benzyl Alcohols/Benzyl Methyl Ethers, and Ammonium Acetate toward Synthesis of Benzoxazoles
inferred← citeshttps://doi.org/10.1021/cr200058fopenalex-snapshot
Constituents from Salvia Species and Their Biological Activities
inferred← citeshttps://doi.org/10.1021/jacs.8b08135openalex-snapshot
Direct and Regioselective C–H Oxidative Difluoromethylation of Heteroarenes
inferred← citeshttps://doi.org/10.1021/jf500802xopenalex-snapshot
Pyrrole Alkaloids with Potential Cancer Chemopreventive Activity Isolated from a Goji Berry-Contaminated Commercial Sample of African Mango
inferred← citeshttps://doi.org/10.1021/jo3022956openalex-snapshot
Reaction of 1-Nitroso-2-naphthols with α-Functionalized Ketones and Related Compounds: The Unexpected Formation of Decarbonylated 2-Substituted Naphtho[1,2- d ][1,3]oxazoles
inferred← citeshttps://doi.org/10.1021/jo500604xopenalex-snapshot
Synthesis of Benzoxazoles from 2-Aminophenols and β-Diketones Using a Combined Catalyst of Brønsted Acid and Copper Iodide
inferred← citeshttps://doi.org/10.1021/jo501216hopenalex-snapshot
Organocatalytic Syntheses of Benzoxazoles and Benzothiazoles using Aryl Iodide and Oxone via C–H Functionalization and C–O/S Bond Formation
inferred← citeshttps://doi.org/10.1021/jo702145dopenalex-snapshot
Copper-Catalyzed Domino Annulation Approaches to the Synthesis of Benzoxazoles under Microwave-Accelerated and Conventional Thermal Conditions
inferred← citeshttps://doi.org/10.1021/ol202844copenalex-snapshot
A Divergent and Selective Synthesis of Isomeric Benzoxazoles from a Single N–Cl Imine
inferred← citeshttps://doi.org/10.1021/ol5031074openalex-snapshot
Efficient Synthesis of Heterocyle-Fused β-Naphthylamines via Intramolecular Addition to a Cyano Group Initiated by Nucleopalladation of Alkynes
inferred← citeshttps://doi.org/10.1038/s41401-024-01399-1openalex-snapshot
A derivative of tanshinone IIA and salviadione, 15a, inhibits inflammation and alleviates DSS-induced colitis in mice by direct binding and inhibition of RIPK2
inferred← citeshttps://doi.org/10.1039/b516326aopenalex-snapshot
Diterpenoids
inferred← citeshttps://doi.org/10.1039/b516351jopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/b718045bopenalex-snapshot
Muscarine, imidazole, oxazole and thiazole alkaloids
inferred← citeshttps://doi.org/10.1039/c0ob00454eopenalex-snapshot
Direct transition-metal-free intramolecular C–O bond formation: synthesis of benzoxazole derivatives
inferred← citeshttps://doi.org/10.1039/c3gc40954fopenalex-snapshot
An efficient electrochemical method for the atom economical synthesis of some benzoxazole derivatives
inferred← citeshttps://doi.org/10.1039/c3gc42499eopenalex-snapshot
Palladium-catalyzed synthesis of benzoxazoles by the cleavage reaction of carbon–carbon triple bonds with o-aminophenol
inferred← citeshttps://doi.org/10.1039/c4ay00562gopenalex-snapshot
Chemical fingerprint analysis of Salvia yunnanensis roots by high-performance liquid chromatography with photodiode array detection
inferred← citeshttps://doi.org/10.1039/c4ob02224fopenalex-snapshot
Synthesis of 4-substituted oxazolo[4,5-c]quinolines by direct reaction at the C-4 position of oxazoles
inferred← citeshttps://doi.org/10.1039/c6nj02293fopenalex-snapshot
A comparative study of the catalytic activity of Co- and CoFe 2 O 4 -NPs in C–N and C–O bond formation: synthesis of benzimidazoles and benzoxazoles from o-haloanilides
inferred← citeshttps://doi.org/10.1039/c6ob00968aopenalex-snapshot
Diacetoxyiodobenzene assisted C–O bond formation via sequential acylation and deacylation process: synthesis of benzoxazole amides and their mechanistic study by DFT
inferred← citeshttps://doi.org/10.1039/c7cc00927eopenalex-snapshot
Electrochemical synthesis of benzoxazoles from anilides – a new approach to employ amidyl radical intermediates
inferred← citeshttps://doi.org/10.1039/c7cc04965jopenalex-snapshot
Iron-catalyzed synthesis of benzoxazoles by oxidative coupling/cyclization of phenol derivatives with benzoyl aldehyde oximes
inferred← citeshttps://doi.org/10.1039/c8np00051dopenalex-snapshot
2-Formylpyrrole natural products: origin, structural diversity, bioactivity and synthesis
inferred← citeshttps://doi.org/10.1039/c9ob01598aopenalex-snapshot
Benzannulated spiroketal natural products: isolation, biological activity, biosynthesis, and total synthesis
inferred← citeshttps://doi.org/10.1039/c9sc00086kopenalex-snapshot
Biomimetic synthesis of the natural product salviadione and its hybrids: discovery of tissue-specific anti-inflammatory agents for acute lung injury
inferred← citeshttps://doi.org/10.1039/d0ob00225aopenalex-snapshot
Base-promoted Lewis acid catalyzed synthesis of quinazoline derivatives
inferred← citeshttps://doi.org/10.1039/d2qo00557copenalex-snapshot
General and practical synthesis of naphtho[2,1- d ]oxazoles from naphthols and amines
inferred← citeshttps://doi.org/10.1039/d2qo01723gopenalex-snapshot
Transition-metal-free oxidative annulation reactions between N -acyl-2-aminoacetophenones and alkynes for the facile synthesis of 2-amino-1-naphthols
inferred← citeshttps://doi.org/10.1039/d3qo00409kopenalex-snapshot
Novel dual-enzyme system for synthesis of 2-alkyl and 2-arylbenzoxazoles via aerobic oxidation
inferred← citeshttps://doi.org/10.1039/d3ra03871hopenalex-snapshot
Advances in the synthetic strategies of benzoxazoles using 2-aminophenol as a precursor: an up-to-date review
inferred← citeshttps://doi.org/10.1039/d5ra09855fopenalex-snapshot
Manganese-catalyzed dehydroxyamination of catechols for the synthesis of redox-active and heterocyclic scaffolds
inferred← citeshttps://doi.org/10.1039/d6qo00276eopenalex-snapshot
Cascade reaction of 2-halo-4-alkenyloxazoles with arynes: a switchable divergent synthesis of 2-arylnaphtho[2,1- d ]oxazoles, N -acylnaphthylamines, and α-halonaphthalenes
inferred← citeshttps://doi.org/10.1080/00397911.2015.1062514openalex-snapshot
Water-Mediated Synthesis of Benzazole and Thiourea Motifs by Reacting Naturally Occurring Isothiocyanate with Amines
inferred← citeshttps://doi.org/10.1080/00397911.2019.1665183openalex-snapshot
Metal free montmorillonite KSF clay catalyzed practical synthesis of benzoxazoles and benzothiazoles under aerobic conditions
inferred← citeshttps://doi.org/10.1080/00397911.2021.1949476openalex-snapshot
TEMPO-mediated aerobic oxidative synthesis of 2-aryl benzoxazoles via ring-opening of benzoxazoles with benzylamines
inferred← citeshttps://doi.org/10.1080/00397911.2025.2535655openalex-snapshot
Design, synthesis, antimicrobial evaluation, in-silico molecular docking, and ADME-T evaluation of novel benzoxazole-piperazine hybrids with amide linkage
inferred← citeshttps://doi.org/10.1080/02678292.2023.2259849openalex-snapshot
Synthesis and mesomorphic properties of bent liquid crystals containing triazole mesogenic unit with terminal flexible alkyl chain and laterally ethoxy substituted Schiff base
inferred← citeshttps://doi.org/10.1080/07352689.2021.1935719openalex-snapshot
Biosynthesis and Regulatory Mechanisms of Bioactive Compounds in Salvia miltiorrhiza, a Model System for Medicinal Plant Biology
inferred← citeshttps://doi.org/10.1080/10286020.2011.600251openalex-snapshot
Sesquiterpenoids and other constituents from the flower buds ofTussilago farfara
inferred← citeshttps://doi.org/10.1080/10286020.2019.1645132openalex-snapshot
Two new tanshinone derivatives from the rhizomes of Salvia miltiorrhiza and their antiviral activities
inferred← citeshttps://doi.org/10.1080/14786419.2019.1596098openalex-snapshot
Diterpenoids isolated from the root of Salvia miltiorrhiza and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1080/17518253.2014.895862openalex-snapshot
Efficient one-pot synthesis of benzoxazole derivatives catalyzed by Zinc triflate
inferred← citeshttps://doi.org/10.1111/jfbc.14208openalex-snapshot
Solid‐state‐cultured mycelium of Antrodia camphorata exerts potential neuroprotective activities against 6‐hydroxydopamine‐induced toxicity in PC12 cells
inferred← citeshttps://doi.org/10.1155/2017/5985703openalex-snapshot
Cryptotanshinone Regulates Androgen Synthesis through the ERK/c‐Fos/CYP17 Pathway in Porcine Granulosa Cells
inferred← citeshttps://doi.org/10.1177/1934578x1100600501openalex-snapshot
Bioactivity-guided Study of Antiproliferative Activities of Salvia Extracts
inferred← citeshttps://doi.org/10.1186/s12906-021-03209-1openalex-snapshot
Comparative study of Danshen and Siwu decoction based on the molecular structures of the components and predicted targets
inferred← citeshttps://doi.org/10.13005/ojc/370211openalex-snapshot
Dowex 50W: A Green Mild Reusable Catalyst for the Synthesis of 2-Aryl Benzoxazole Derivatives in Aqueous Medium
inferred← citeshttps://doi.org/10.14233/ajchem.2020.22745openalex-snapshot
Microwave-assisted Synthesis of 2-Substituted Naphtho[1,2-d][1,3]oxazoles by Reacting 1-Nitroso-2-naphthol with Allyl Bromides and Benzyl Bromides using FeCl3 as Catalyst
inferred← citeshttps://doi.org/10.1515/ntrev-2017-0138openalex-snapshot
Cobalt ferrite nanoparticles (CoFe2O4 MNPs) as catalyst and support: magnetically recoverable nanocatalysts in organic synthesis
inferred← citeshttps://doi.org/10.1517/13543776.2013.736494openalex-snapshot
Tanshinone derivatives: a patent review (January 2006 – September 2012)
inferred← citeshttps://doi.org/10.2174/1568026620666200922115109openalex-snapshot
Synthesis and Biological Activity Study of Tanshinone Derivatives: A Literature and Patent Review
inferred← citeshttps://doi.org/10.2174/1570193x15666180627125007openalex-snapshot
Exploration of the Biological Potential of Benzoxazoles: An Overview
inferred← citeshttps://doi.org/10.3184/174751912x13360692916944openalex-snapshot
Synthesis of Benzoxazoles by the Copper Triflate Catalysed Reaction of Nitriles and O-Aminophenols
inferred← citeshttps://doi.org/10.32508/stdjns.v7i2.1259openalex-snapshot
Pyrrole-type compounds from the flowers of Calotropis gigantea
inferred← citeshttps://doi.org/10.3389/fmicb.2015.00856openalex-snapshot
Mangrove rare actinobacteria: taxonomy, natural compound, and discovery of bioactivity
inferred← citeshttps://doi.org/10.3390/foods14091646openalex-snapshot
Nitraria sibirica Pall.: A Halophytic Resource for Antioxidant-Rich Functional Foods and Ecological Resilience
inferred← citeshttps://doi.org/10.3390/md12010477openalex-snapshot
Alkaloids from the Mangrove-Derived Actinomycete Jishengella endophytica 161111
inferred← citeshttps://doi.org/10.3390/molecules28020821openalex-snapshot
Genomics-Driven Discovery of Benzoxazole Alkaloids from the Marine-Derived Micromonospora sp. SCSIO 07395
inferred← citeshttps://doi.org/10.3390/molecules28062599openalex-snapshot
Pyrrole-2-carboxaldehydes: Origins and Physiological Activities
inferred← citeshttps://doi.org/10.3390/pathogens11070795openalex-snapshot
Pathogenicity and Metabolites of Purpureocillium lavendulum YMF1.00683 against Meloidogyne incognita
inferred← citeshttps://doi.org/10.3390/ph16070909openalex-snapshot
Investigation of Novel Benzoxazole-Oxadiazole Derivatives as Effective Anti-Alzheimer’s Agents: In Vitro and In Silico Approaches
inferred← citeshttps://doi.org/10.37952/roi-jbc-01/19-59-8-40openalex-snapshot
Quantum-chemical simulation of the interaction of 2-methyl-5,7-dinitrobenzo[d]oxazole with tetrahydride borate ion by DFT method
inferred← citeshttps://doi.org/10.4018/979-8-3693-9112-9.ch013openalex-snapshot
Medicinal Uses of Secondary Metabolites in the Genus Salvia
inferred← citeshttps://doi.org/10.6084/m9.figshare.13633023openalex-snapshot
Additional file 1 of Comparative study of Danshen and Siwu decoction based on the molecular structures of the components and predicted targets
inferred← citeshttps://doi.org/10.6084/m9.figshare.13633026openalex-snapshot
Additional file 2 of Comparative study of Danshen and Siwu decoction based on the molecular structures of the components and predicted targets
inferred← citeshttps://doi.org/10.6084/m9.figshare.13633029openalex-snapshot
Additional file 3 of Comparative study of Danshen and Siwu decoction based on the molecular structures of the components and predicted targets
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.