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Volumn 57, Issue 40, 2001, Pages 8425-8442
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Common synthetic strategy for optically active cyclic terpenoids having a 1,1,5-trimethyl-trans-decalin nucleus: Syntheses of (+)-acuminolide, (-)-spongianolide A, and (+)-scalarenedial
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Author keywords
1,1,5 trimethyl trans decalin nucleus; Biologically active compounds; Common synthetic strategy; Terpenes and terpenoiods
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Indexed keywords
ACETAL;
ACID;
ACUMINOLIDE;
ALKENE;
BETA KETOESTER DERIVATIVE;
ESTER DERIVATIVE;
NEOUVARIA ACUMINATISSIMA EXTRACT;
PLANT EXTRACT;
SCALARENEDIAL;
SPONGIANOLIDE A;
TERPENOID DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL REACTION;
CHIRALITY;
CONTROLLED STUDY;
CYCLIZATION;
DRUG ACTIVITY;
DRUG PURITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENANTIOMER;
NONHUMAN;
OPTICAL ROTATION;
PLANT;
PRIORITY JOURNAL;
REACTION ANALYSIS;
STEREOCHEMISTRY;
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EID: 0035478120
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(01)00825-0 Document Type: Article |
Times cited : (35)
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References (44)
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