A short synthetic route to (+)-austamide, (+)-deoxyisoaustamide, and (+)-hydratoaustamide from a common precursor by a novel palladium-mediated indole→dihydroindoloazocine cyclization

Journal of the American Chemical Society

Volumn 124, Issue 27, 2002, Pages 7904-7905

  Baran, Phil S ^a   Corey, E J ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; AUSTAMIDE; AZOCINE DERIVATIVE; DEOXYISOAUSTAMIDE; DIHYDROINDOLOAZOCINE; HYDRATOAUSTAMIDE; INDOLE DERIVATIVE; PALLADIUM; TRYPTOPHAN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL STRUCTURE; CHROMATOGRAPHY; CYCLIZATION; ENANTIOSELECTIVITY; HYDROXYLATION; REACTION ANALYSIS; REDUCTION; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

AZOCINES; INDOLES; PALLADIUM; STEREOISOMERISM; TRYPTOPHAN;

EID: 0037055075     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja026663t     Document Type: Article

References (16)

1. Biosynthesis of prenylated alkaloids derived from tryptophan