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Journal of the American Chemical Society

Volumn 131, Issue 39, 2009, Pages 13928-13929

A short enantioselective total synthesis of the fundamental pentacyclic triterpene lupeol

(2) Surendra, Karavadhi a Corey, E J a

a HARVARD UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; ENANTIOSELECTIVE SYNTHESIS; ENANTIOSELECTIVE TOTAL SYNTHESIS; NATURAL PRODUCT SYNTHESIS; STEREOCONTROL; TRITERPENES;

CHEMICAL REACTIONS;

18 EPI BETA AMYRIN; ALPHA AMYRIN; DELTA AMYRIN; GERMANICOL; LUPEOL; PENTACYCLIC TRITERPENE; PSI TARAXASTEROL; TARAXASTEROL; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; ENANTIOSELECTIVITY; PROTON NUCLEAR MAGNETIC RESONANCE;

CYCLIZATION; MOLECULAR STRUCTURE; PENTACYCLIC TRITERPENES; STEREOISOMERISM;

EID: 70349623190 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja906335u Document Type: Article

Times cited : (78)

References (13)

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- note
- 1H NMR data and time course studies of the acidcatalyzed rearrangement of lupeol, see: Supporting Information.

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