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Issue 17, 2003
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Total asymmetric synthesis of sperabillins B and D

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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

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Publication details

The article was received on 22 May 2003, accepted on 08 Jul 2003 and first published on 21 Jul 2003


Article type: Communication
DOI: 10.1039/B305740B
Citation: Chem. Commun., 2003,0, 2132-2133
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    Total asymmetric synthesis of sperabillins B and D

    S. G. Davies, R. J. Kelly and A. J. Price Mortimer, Chem. Commun., 2003, 0, 2132
    DOI: 10.1039/B305740B

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