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Synthesis of the C7-C15 trans decalin portion of the natural antibiotic tetrodecamycin
Journal article   Peer reviewed

Synthesis of the C7-C15 trans decalin portion of the natural antibiotic tetrodecamycin

Jeffrey Warrington and Louis Barriault
Organic letters, Vol.7(21), pp.4589-4592
10/13/2005
PMID: 16209486

Abstract

Anti-Bacterial Agents - chemistry Furans - chemistry Molecular Structure Naphthalenes - chemical synthesis Naphthalenes - chemistry Stereoisomerism
[reaction: see text] The tandem oxy-Cope/ene/Claisen rearrangement has been developed in our laboratory as a powerful method for rapid construction of complex Decalin cores. Herein, we describe the use of this method to generate the Decalin core of the natural antibiotic tetrodecamycin (1) bearing six contiguous stereocenters.

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