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Short Asymmetric Synthesis of (+)-α-Curcumene and (+)-Xanthorrhizol
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cber.19781110807openalex-snapshot
Brom/Lithium‐Austausch an Vinylbromiden mit 2 Moläquivv. tert‐Butyllithium. Umsetzungen von Vinyllithiumverbindungen mit Hetero‐ und Kohlenstoff‐Elektrophilen
inferredcites →https://doi.org/10.1016/0040-4020(68)88174-8openalex-snapshot
Studies in sesquiterpenes—XXXVII
inferredcites →https://doi.org/10.1016/0040-4020(78)80198-7openalex-snapshot
Structures and synthesis of some new antibacterial sesquiterpenoids from the gorgonian coral Pseudopterogorgia rigida
inferredcites →https://doi.org/10.1016/s0040-4020(01)86178-0openalex-snapshot
Synthesis of (+)-α-curcumene, (+)-curcumone, and (-)-methyl citronellate starting from optically pure 5-trimethylsilyl-2-cyclohexenone
inferredcites →https://doi.org/10.1016/s0040-4020(01)90579-4openalex-snapshot
Applications of the intramolecular diels-alder reactions of heterodienes to the syntheses of indole alkaloids
inferredcites →https://doi.org/10.1016/s0040-4039(00)61579-4openalex-snapshot
An asymmetric synthesis of a C2 symmetric tetrasubstituted biaryl: 2,2′-Dihydroxy-6,6′-dimethyl-1,1′-biphenyl, a stable chiral system
inferredcites →https://doi.org/10.1016/s0040-4039(01)80984-9openalex-snapshot
1,2-bis(diphenylphosphino)ethane tetrahalide: A convenient reagent for the conversion of alcohols to the corresponding halides
inferredcites →https://doi.org/10.1016/s0040-4039(01)86288-2openalex-snapshot
Asymmetric total synthesis of optically active α-curcumene
inferredcites →https://doi.org/10.1016/s0040-4039(01)86405-4openalex-snapshot
A total asymmetric synthesis of (+)-ar-turmerone
inferredcites →https://doi.org/10.1021/ja00178a037openalex-snapshot
Asymmetric total synthesis of dibenzocyclooctadiene lignans (-)-schizandrin and (-)-isoschizandrin. Structure revision of (+)-isoschizandrin
inferredcites →https://doi.org/10.1021/ja00245a031openalex-snapshot
Eudistomins A-Q, .beta.-carbolines from the antiviral Caribbean tunicate Eudistoma olivaceum
inferredcites →https://doi.org/10.1021/ja01129a002openalex-snapshot
Studies in Stereochemistry. VI. The Mechanisms of the E1 and Hydrogen Migration Reactions in the 3-Phenyl-2-butanol System
inferredcites →https://doi.org/10.1021/jo00025a027openalex-snapshot
Asymmetric Michael additions to .alpha.,.beta.-unsaturated oxazolines. An efficient preparation of chiral .beta.,.beta.-disubstituted propionaldehydes
inferredcites →https://doi.org/10.1021/jo01327a046openalex-snapshot
Highly stereoselective addition of organolithium reagents to chiral oxazolines. Asymmetric synthesis of 3-substituted alkanoic acids and 3-substituted lactones
inferredcites →https://doi.org/10.1021/np50054a007openalex-snapshot
Perezone and Related Sesquiterpenes from Parvifoline
inferredcites →https://doi.org/10.1246/cl.1985.1153openalex-snapshot
A NOVEL SYNTHETIC METHOD OF OPTICALLY PURE α-SUBSTITUTED ALDEHYDE ACETALS BY THE USE OF REDUCTIVE 1,2-REARRANGEMENT
inferredcites →https://doi.org/10.1246/cl.1989.1781openalex-snapshot
Enantiodivergent Route to the Aromatic Bisabolane Sesquiterpenes via a Chiral Acetylene Alcohol
inferredcites →https://doi.org/10.1515/znb-1970-0917openalex-snapshot
Xanthorrhizol, ein neues Sesquiterpen aus Curcuma xanthorrhiza
inferredcites →https://doi.org/10.3987/com-96-7445openalex-snapshot
A Formal Total Synthesis of Xanthorrhizol Based on Nucleophilic Openig of Vinyloxirane by Arylcopper Reagent
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Secondary Metabolites with Anti-Inflammatory Activity from Marine-Derived Fungus Biscogniauxia Sp. 8703
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19990601)111:11<1721::aid-ange1721>3.0.co;2-copenalex-snapshot
Chiralitätstransfer bei der Elektronentransfer-getriebenen benzylischen Umpolung von Aren-Cr(CO)3-Komplexen
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The Catalytic, Enantioselective Michael Reaction
inferred← citeshttps://doi.org/10.1002/ange.200390220openalex-snapshot
Phospholane–Oxazoline Ligands for Ir‐Catalyzed Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/ange.200604810openalex-snapshot
Rh‐Catalyzed Highly Enantioselective Synthesis of 3‐Arylbutanoic Acids
inferred← citeshttps://doi.org/10.1002/ange.201107802openalex-snapshot
Enantioselective Iridium‐Catalyzed Hydrogenation of β,γ‐Unsaturated Carboxylic Acids: An Efficient Approach to Chiral 4‐Alkyl‐4‐aryl Butanoic Acids
inferred← citeshttps://doi.org/10.1002/anie.200390251openalex-snapshot
Phospholane–Oxazoline Ligands for Ir‐Catalyzed Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1002/anie.200604810openalex-snapshot
Rh‐Catalyzed Highly Enantioselective Synthesis of 3‐Arylbutanoic Acids
inferred← citeshttps://doi.org/10.1002/anie.201107802openalex-snapshot
Enantioselective Iridium‐Catalyzed Hydrogenation of β,γ‐Unsaturated Carboxylic Acids: An Efficient Approach to Chiral 4‐Alkyl‐4‐aryl Butanoic Acids
inferred← citeshttps://doi.org/10.1002/asia.201400049openalex-snapshot
Asymmetric Decarboxylative 1,4‐Addition of Malonic Acid Half Thioesters to Vinyl Sulfones: Highly Enantioselective Synthesis of 3‐Monofluoromethyl‐3‐Arylpropanoic Esters
inferred← citeshttps://doi.org/10.1002/chem.201705463openalex-snapshot
Cobalt‐Catalyzed Enantioselective Negishi Cross‐Coupling of Racemic α‐Bromo Esters with Arylzincs
inferred← citeshttps://doi.org/10.1002/chem.202101863openalex-snapshot
Total Synthesis of (+)‐Erogorgiaene and the Pseudopterosin A−F Aglycone via Enantioselective Cobalt‐Catalyzed Hydrovinylation
inferred← citeshttps://doi.org/10.1002/chin.199749205openalex-snapshot
ChemInform Abstract: Short Asymmetric Synthesis of (+)‐α‐Curcumene and (+)‐ Xanthorrhizol.
inferred← citeshttps://doi.org/10.1002/ejoc.202200058openalex-snapshot
Total Synthesis and Antibiotic Properties of Amino‐Functionalized Aromatic Terpenoids Related to Erogorgiaene and the Pseudopterosins
inferred← citeshttps://doi.org/10.1002/hlca.201000111openalex-snapshot
Efficient Total Synthesis of Racemic Bisabolane Sesquiterpenes Curcuphenol and Xanthorrhizol Starting from Substituted Acetophenones
inferred← citeshttps://doi.org/10.1016/b978-0-12-417034-6.00008-6openalex-snapshot
Conjugate Addition II
inferred← citeshttps://doi.org/10.1016/j.cclet.2025.111023openalex-snapshot
SOP-ligand enabled palladium-catalyzed enantioselective anti-Markovnikov hydrothioesterification of α-substituted styrenes
inferred← citeshttps://doi.org/10.1016/j.tet.2003.09.065openalex-snapshot
Recent synthetic uses of functionalised aromatic and heteroaromatic organolithium reagents prepared by non-deprotonating methods
inferred← citeshttps://doi.org/10.1016/j.tet.2005.03.111openalex-snapshot
A new class of readily available and conformationally rigid phosphino-oxazoline ligands for asymmetric catalysis
inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.10.041openalex-snapshot
Asymmetric synthesis of 5,6-dehydrosenedigitalene using lipase-catalyzed highly enantioselective transesterification of a primary alcohol with vinyl 3-(4-trifluoromethylphenyl)propanoate
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.10.019openalex-snapshot
Enantioselective synthesis of (R)- and (S)-curcumene and curcuphenol: an efficient chemoenzymatic route
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.11.051openalex-snapshot
Chemistry of xanthorrhizol: synthesis of several bisabolane sesquiterpenoids from xanthorrhizol
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.117openalex-snapshot
An expeditious protocol for sesquiterpene-cored functionalized arenes from S-(−)-citronellal
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.12.017openalex-snapshot
Diastereoselective hydrogenation of α,β-unsaturated but-2-enamides to access the chiral 3-(p-tolyl) butanoic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155656openalex-snapshot
Asymmetric approach to aromatic bisabolanes via allylic diazene rearrangement (ADR): Total syntheses of (−)-curcumene, (−)-dihydrocurcumene, (−)-nuciferol, and (−)-nuciferal
inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00081-3openalex-snapshot
(+)-Bisabola-2,10-diene[1,9]oxide, a constituent of the liverwort Calypogeia suecica
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)01151-6openalex-snapshot
Asymmetric conjugate additions to chiral α,β-unsaturated oxazolines with sulfonyl carbanions
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)01882-3openalex-snapshot
Benzothiazines in synthesis. Formal syntheses of (+)-curcumene and (+)-curcuphenol
inferred← citeshttps://doi.org/10.1016/s0957-4166(02)00759-0openalex-snapshot
Total asymmetric synthesis of (7S,9R)-(+)-bisacumol
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02104openalex-snapshot
Palladium-Catalyzed Diastereoselective Synthesis of 3-Arylbutanoic Acid Derivatives
inferred← citeshttps://doi.org/10.1021/jo0351318openalex-snapshot
Stereospecific Pd(0)-Catalyzed Arylation of an Allylic Hydroxy Phosphonate Derivative: Formal Synthesis of (S)-(+)-ar-Turmerone
inferred← citeshttps://doi.org/10.1021/jo902066yopenalex-snapshot
trans-Directing Ability of the Amide Group: Enabling the Enantiocontrol in the Synthesis of 1,1-Dicarboxy Cyclopropanes. Reaction Development, Scope, and Synthetic Applications
inferred← citeshttps://doi.org/10.1021/jo981341mopenalex-snapshot
Stereocontrol between Remote Atom Centers in Acyclic Substrates. Anti Addition of Hydride to 1,5-, 1,6-, and 1,7-Hydroxy Ketones
inferred← citeshttps://doi.org/10.1021/ol0259847openalex-snapshot
Pseudoephedrine as a Chiral Auxiliary for Asymmetric Michael Reactions: Synthesis of 3-Aryl-δ-lactones
inferred← citeshttps://doi.org/10.1021/ol0362717openalex-snapshot
Synthesis of a New Class of Conformationally Rigid Phosphino-oxazolines: Highly Enantioselective Ligands for Ir-Catalyzed Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1021/ol048790vopenalex-snapshot
Chiral Benzyl Centers through Asymmetric Catalysis. A Three-Step Synthesis of (R)-(−)-α-Curcumene via Asymmetric Hydrovinylation
inferred← citeshttps://doi.org/10.1039/a802867bopenalex-snapshot
Main group organometallics in organic synthesis
inferred← citeshttps://doi.org/10.1039/a808772eopenalex-snapshot
Baker’s yeast mediated enantioselective synthesis of the bisabolane sesquiterpenes curcumene, turmerone, dehydrocurcumene and nuciferal
inferred← citeshttps://doi.org/10.1039/b000155oopenalex-snapshot
The control of remote asymmetric centres via reduction of acyclic carbonyl functions
inferred← citeshttps://doi.org/10.1039/b006141gopenalex-snapshot
Baker’s yeast-mediated enantioselective synthesis of the bisabolane sesquiterpenes (+)-curcuphenol, (+)-xanthorrhizol, (−)-curcuquinone and (+)-curcuhydroquinone
inferred← citeshttps://doi.org/10.1039/c3qo00042gopenalex-snapshot
Asymmetric hydrogenation of α-arylacrylic and β-arylbut-3-enoic acids catalyzed by a Rh(i) complex of a monodentate secondary phosphine oxide ligand
inferred← citeshttps://doi.org/10.1039/d1fo01212fopenalex-snapshot
Bisabolane-type sesquiterpenoids from Curcuma longa L. exert anti-influenza and anti-inflammatory activities through NF-κB/MAPK and RIG-1/STAT1/2 signaling pathways
inferred← citeshttps://doi.org/10.1080/10286020.2025.2576000openalex-snapshot
Secondary metabolites with anti-inflammatory activity isolated from a marine-derived fungus Biscogniauxia sp. 8703
inferred← citeshttps://doi.org/10.1080/14786419.2023.2222219openalex-snapshot
Potent nitric oxide inhibitory sesquiterpenoids from the rhizome of Curcuma aromatica Salisb.
inferred← citeshttps://doi.org/10.1177/1934578x1100600203openalex-snapshot
Facile Total Synthesis of Xanthorrhizol
inferred← citeshttps://doi.org/10.1248/cpb.55.1361openalex-snapshot
Synthesis of (R)-Curcumene and (R)-Xanthorrizol Based on 1,2-Aryl Migration via Phenonium Ion
inferred← citeshttps://doi.org/10.3358/shokueishi.48.106openalex-snapshot
Antimicrobial Activity and Constituents in Rumput Roman Extract as a Natural Food Preservative
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A Short Synthesis of Bisabolane Sesquiterpenes
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Preparation of a furfural-derived enantioenriched vinyloxazoline building block and exploring its reactivity
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Activation et transformation catalytique de SO₂ par des composés organométalliques et organiques
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