Straightforward synthesis of indolizidine alkaloid 167B

Tetrahedron Letters

Volumn 51, Issue 48, 2010, Pages 6290-6293

  Gracia, Stéphanie ^a   Jerpan, Rudolf ^a   Pellet Rostaing, Stéphane ^a   Popowycz, Florence ^a   Lemaire, Marc ^a  

^a UNIVERSITÉ LYON 1   (France)

Author keywords

Alkaloids; Indolizidines; Michael addition; Multi step synthesis

Indexed keywords

INDOLIZIDINE ALKALOID;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; MICHAEL ADDITION; STEREOCHEMISTRY; SYNTHESIS;

EID: 78049360991     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.09.105     Document Type: Article

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68. 4, and evaporated to afford indolizidines 6a-c.
69. 5-Propylindolizidine 6c (Indolizidine 167B) was obtained as a colorless oil (yield 91%; dr = 85% measured by NMR) and analytical data were found to correspond with data reported in the literature.