Enantioselective synthesis of curacin A. 2. Total synthesis of curacin A by condensation of C1-C7, C8-C17, and C18-C22 segments

Hisanaka Ito, Nobuyuki Imai, Ken Ichi Takao, Susumu Kobayashi

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Total synthesis of curacin A, a novel antimitotic antiproliferative antibiotic, was achieved by the connection of C1-C7, C8-C17, and C18-C22 segments by Julia coupling and iminoether condensation.

Original languageEnglish
Pages (from-to)1799-1800
Number of pages2
JournalTetrahedron Letters
Volume37
Issue number11
DOIs
Publication statusPublished - 1996 Mar 11
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Enantioselective synthesis of curacin A. 2. Total synthesis of curacin A by condensation of C1-C7, C8-C17, and C18-C22 segments'. Together they form a unique fingerprint.

  • Cite this