Issue 1, 1989
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Enantioselective synthesis of the C1,6-C21,16 segment of macbecins I and II

Raymond Baker  and  Jose L. Castro  

Abstract

A highly efficient and stereocontrolled enantioselective synthesis of the C1,6-C21,16segment of macbecins I and II has been performed in 19 steps and 28.5% overall yield.

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Article information

DOI
https://doi.org/10.1039/P19890000190
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 190-192

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Enantioselective synthesis of the C1,6-C21,16 segment of macbecins I and II

R. Baker and J. L. Castro, J. Chem. Soc., Perkin Trans. 1, 1989, 190 DOI: 10.1039/P19890000190

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