Total synthesis of (±)-epimagnolin A

The first total synthesis of (±)-epimagnolin A was achieved employing a C–H insertion reaction to generate selectively the bicyclic framework with the exo, endo-stereochemistry. Graphic

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Bibliographic Details
Published in:Tetrahedron letters 2001-01, Vol.42 (3), p.473-475
Main Authors: Brown, Richard C.D, Bataille, Carole J.R, Hinks, Jeremy D
Format: Article
Language:English
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Description
Summary:The first total synthesis of (±)-epimagnolin A was achieved employing a C–H insertion reaction to generate selectively the bicyclic framework with the exo, endo-stereochemistry. Graphic
ISSN:0040-4039
1873-3581
DOI:10.1016/S0040-4039(00)01958-4