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Angewandte Chemie - International Edition

Volumn 41, Issue 12, 2002, Pages 2188-2191

A stereoselective route to guanacastepene A through a surprising epoxidation

(4) Lin, Songnian c Dudley, Gregory B c Tan, Derek S c Danishefsky, Samuel J a,b

a MEMORIAL SLOAN KETTERING CANCER CENTER (United States)

b Och Spine at New York Presbyterian Hospitals (United States)

c NONE

Author keywords

Antibiotics; Diastereoselectivity; Epoxidation; Natural products; Total synthesis

Indexed keywords

EPOXIDATION;

OXIDATION; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

AROMATIC COMPOUNDS;

DITERPENE; GUANACASTEPENE A; UNCLASSIFIED DRUG;

ACETYLATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DIASTEREOISOMER; EPOXIDATION; HYDROXYLATION; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; PYROLYSIS; STEREOCHEMISTRY; SYNTHESIS;

DITERPENES; EPOXY COMPOUNDS; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 0037124683 PISSN: 14337851 EISSN: None Source Type: Journal
DOI: 10.1002/1521-3773(20020617)41:12<2188::AID-ANIE2188>3.0.CO;2-J Document Type: Article

Times cited : (72)

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