Enantiospecific and stereoselective synthesis of (−)-allosedamine

A total synthesis of (−)-allosedamine (>99% ee, de) is described in 14 steps with an overall yield of 29% from benzaldehyde. Graphic

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Bibliographic Details
Published inTetrahedron letters Vol. 43; no. 2; pp. 225 - 227
Main Authors Felpin, François-Xavier, Lebreton, Jacques
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 07.01.2002
Elsevier
Subjects
Chemistry
Chemistry, Organic
Physical Sciences
Science & Technology
ALCOHOLS
CYCLOADDITION
CHIRAL SYNTHESIS
CARBONATES
ORGANOBORANES
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Summary:A total synthesis of (−)-allosedamine (>99% ee, de) is described in 14 steps with an overall yield of 29% from benzaldehyde. Graphic
ISSN:0040-4039
1873-3581
DOI:10.1016/S0040-4039(01)02105-0