4.6 Article

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

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 6, Issue 24, Pages 4502-4504

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b814882a

Keywords

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Funding

  1. Ministerio de Educacion y Ciencia, Spain
  2. DGI [CTQ2005-03124]

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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.

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