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Issue 24, 2008
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Asymmetric sulfur ylide based enantioselective synthesis of D-erythro-sphingosine

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Abstract

An asymmetric sulfur ylide reaction was employed to prepare an epoxide intermediate in a convergent manner. This epoxide was efficiently transformed into D-erythro-sphingosine.

Graphical abstract: Asymmetric sulfur ylide based enantioselective synthesis of D-erythro-sphingosine

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Article information


Submitted
26 Aug 2008
Accepted
01 Oct 2008
First published
17 Oct 2008

Org. Biomol. Chem., 2008,6, 4502-4504
Article type
Communication

Asymmetric sulfur ylide based enantioselective synthesis of D-erythro-sphingosine

J. A. Morales-Serna, J. Llaveria, Y. Díaz, M. I. Matheu and S. Castillón, Org. Biomol. Chem., 2008, 6, 4502
DOI: 10.1039/B814882A

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