SYNTHETIC STUDY OF MARINE MACROLIDE SWINHOLIDE A. STEREOCONTROLLED SYNTHESIS OF THE C11-C32 SEGMENT

Abstract

The C24-C32 segment 4 of swinholide A (1) was stereoselectively synthesized starting from (S)-methyl 3-hydroxybutyrate, and the convergent synthesis of the C11-C32 segment 5 was accomplished via stereoselective aldol condensation of 3 and 4

Journal

Chemical & pharmaceutical bulletin   [List of Volumes]

Chemical & pharmaceutical bulletin 42(11), 2403-2405, 1994-11-15  [Table of Contents]

The Pharmaceutical Society of Japan

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Codes

  • NII Article ID (NAID) :
    110003630860
  • NII NACSIS-CAT ID (NCID) :
    AA00602100
  • Text Lang :
    ENG
  • ISSN :
    00092363
  • Databases :
    NII-ELS 

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