Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 17, 2003
Previous Article Next Article

Total asymmetric synthesis of sperabillins B and D

Author affiliations

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

Back to tab navigation

Supplementary files

Article information


Submitted
22 May 2003
Accepted
08 Jul 2003
First published
21 Jul 2003

Chem. Commun., 2003, 2132-2133
Article type
Communication

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

Social activity

Search articles by author

Spotlight

Advertisements