Issue 17, 2003

Total asymmetric synthesis of sperabillins B and D

Abstract

A consise route to the core fragment of sperabillins B and D, methyl (3R,5R,6R)-3,6-diamino-5-hydroxyheptanoate, has been developed with a subsequent novel protection strategy allowing the total asymmetric synthesis of sperabillins B and D.

Graphical abstract: Total asymmetric synthesis of sperabillins B and D

Supplementary files

Article information

Article type
Communication
Submitted
22 May 2003
Accepted
08 Jul 2003
First published
21 Jul 2003

Chem. Commun., 2003, 2132-2133

Total asymmetric synthesis of sperabillins B and D

S. G. Davies, R. J. Kelly and A. J. Price Mortimer, Chem. Commun., 2003, 2132 DOI: 10.1039/B305740B

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