Enantioselective synthesis of cadinanes starting from R-(−)- or S-(+)-carvone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Enantioselective Synthesis, Natural Products from Chiral Terpenes;Ho,1992
2. The conversion of (−)- and (+)-dihydrocarvone into chiral intermediates for the synthesis of (−)-polygodial, (−)-warburganal and (−)-muzigadial
3. Lewis acid catalyzed diels-alder reactions of S-(+)-carvone1 with silyloxy dienes. Total synthesis of (+)-α-cyperone.
4. The synthesis of chiral decalones, (−)-1,1,4a-trimethyl-2-decalol and (+)-geosmin from S-(+)-carvone (part 3)
5. 4,5-Dichloro-1,2,3-dithiazolium chloride (Appel's Salt): Reactions with N-nucleophiles.
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1. Discovery and bioinspired total syntheses of unprecedented sesquiterpenoid dimers unveiled bifurcating [4 + 2] cycloaddition and target differentiation of enantiomers;Chemical Science;2024
2. ChemInform Abstract: Enantioselective Synthesis of Cadinanes Starting from R-(-)- or S-(+)-Carvone.;ChemInform;2010-06-20
3. First total synthesis of 10α-hydroxy-4-muurolen-3-one and its C10-isomer;Chinese Chemical Letters;2008-11
4. THE CONQUEST OF VINIGROL. CREATIVITY, FRUSTRATIONS, AND HOPE;Organic Preparations and Procedures International;2007-08
5. Total Synthesis of 4α,5α,10β-Trihydroxycadinane and Its C4-Isomer: Structural Revision of a Natural Sesquiterpenoid;Synlett;2006-09
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