Total synthesis of lepadins B, D, E, and H; determination of the configuration of the latter three alkaloids

Angewandte Chemie - International Edition

Volumn 43, Issue 32, 2004, Pages 4222-4225

  Pu, Xiaotao ^a   Ma, Dawei ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

Alkaloids; Configuration determination; Hydrogenation; Olefination; Total synthesis

Indexed keywords

SYNTHESIS (CHEMICAL);

ALKALOIDS; BIOLOGICAL ACTIVITY; LEPADINS;

ORGANIC COMPOUNDS;

ALKALOID; KETONE; LEPADIN B; LEPADIN D; LEPADIN E; LEPADIN H; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL BOND; CRYSTAL STRUCTURE; CYCLIZATION; DRUG DETERMINATION; DRUG SYNTHESIS; EPOXIDATION; HORNER WADSWORTH EMMONS REACTION; HYDROLYSIS KINETICS; OLEFINATION; OXIDATION KINETICS; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION KINETICS; RING OPENING; STEREOCHEMISTRY; WITTIG REACTION;

ALKALOIDS; HYDROGENATION; MOLECULAR CONFORMATION; QUINOLINES;

EID: 4544253397     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200460128     Document Type: Article

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