Issue 18, 2003
From the journal:

Organic & Biomolecular Chemistry

An enantioselective synthesis of the C(33)–C(37) fragment of Amphotericin B†

Kaisa Karisalmi,a   Kari Rissanenb  and  Ari M. P. Koskinen*a  

* Corresponding authors

a Laboratory of Organic Chemistry, Helsinki University of Technology, Kemistintie 1, P.O. Box 6100, Fin-02015 HUT Espoo, Finland

b X-Ray crystallography: Laboratory of Organic Chemistry, Department of Chemistry, University of Jyväskylä, P.O. Box 35, Fin-40014, Finland

Abstract

An enantioselective synthesis of the C(33)–C(37) tripropionate fragment of Amphotericin B has been developed in only 6 steps.

Graphical abstract: An enantioselective synthesis of the C(33)–C(37) fragment of Amphotericin B

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Article information

DOI
https://doi.org/10.1039/B305845J
Article type
Paper
Submitted
27 May 2003
Accepted
13 Aug 2003
First published
20 Aug 2003

Org. Biomol. Chem., 2003,1, 3193-3196

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An enantioselective synthesis of the C(33)–C(37) fragment of Amphotericin B

K. Karisalmi, K. Rissanen and A. M. P. Koskinen, Org. Biomol. Chem., 2003, 1, 3193 DOI: 10.1039/B305845J

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