Total synthesis of the C-37-C-45 F-ring fragment of spongistatins
Lemaire-Audoire, S; Vogel, P
1998

Abstract

The highly substituted F ring of Spongistatins was synthesized from (R)-(+)-3-benzyloxy-2-methylpropan-1-ol (5), using two sequential Sharpless dihydroxylations as key-steps. A 4-deoxy-4-methyl-D-threo-L-glucoheptopyranose derivative was obtained and could be used to generate the corresponding allyl beta-C-glycoside. (C) 1998 Elsevier Science Ltd. All rights reserved.

Details

Title Total synthesis of the C-37-C-45 F-ring fragment of spongistatins
Author(s) Lemaire-Audoire, S ; Vogel, P
Published in Tetrahedron Letters
Volume 39
Issue 11
Pages 1345-1348
Date 1998
ISSN 0040-4039
Keywords
DOI https://doi.org/10.1016/S0040-4039(97)10817-6
Laboratories LGSA
Record Appears in Scientific production and competences > SB - School of Basic Sciences > SB Archives > LGSA - Laboratory of Glycochemistry and Asymmetric Synthesis
Peer-reviewed publications
Work produced at EPFL
Journal Articles
Published
Record creation date 2005-11-09

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