Issue 29, 2013

Directed studies towards the total synthesis of (+)-13-deoxytedanolide: simple and convenient synthesis of the C8–C16 fragment

Abstract

A straightforward synthesis of the enantioenriched C8–C16 south part of (+)-13-deoxytedanolide has been reported. The strength of this approach relies on the preparation of similar functionalized fragments via the transformation of a unique dihydrofuran building block through a 1,2-metallate rearrangement.

Graphical abstract: Directed studies towards the total synthesis of (+)-13-deoxytedanolide: simple and convenient synthesis of the C8–C16 fragment

Supplementary files

Article information

Article type
Paper
Submitted
04 Apr 2013
Accepted
21 May 2013
First published
22 May 2013

Org. Biomol. Chem., 2013,11, 4882-4890

Directed studies towards the total synthesis of (+)-13-deoxytedanolide: simple and convenient synthesis of the C8–C16 fragment

S. Meiries, A. Bartoli, M. Decostanzi, J. Parrain and L. Commeiras, Org. Biomol. Chem., 2013, 11, 4882 DOI: 10.1039/C3OB40674A

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