Total synthesis of (+)-sundiversifolide

Hiromasa Yokoe, Hiroyuki Sasaki, Tomoyuki Yoshimura, Mitsuru Shindo, Masahiro Yoshida, Kozo Shishido

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

(Chemical Equation Presented) The first, enantiocontrolled total synthesis of (+)-sundiversifolide has been accomplished using the sequential ring-closing metathesis, [3,3]-sigmatropic rearrangement, and iodolactonization for the key assembly of the cis-fused oxabicyclo[5.3.0]decene framework of the natural product.

Original languageEnglish
Pages (from-to)969-971
Number of pages3
JournalOrganic letters
Volume9
Issue number6
DOIs
Publication statusPublished - Mar 15 2007

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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  • Cite this

    Yokoe, H., Sasaki, H., Yoshimura, T., Shindo, M., Yoshida, M., & Shishido, K. (2007). Total synthesis of (+)-sundiversifolide. Organic letters, 9(6), 969-971. https://doi.org/10.1021/ol062960h