Total Synthesis of Biselyngbyolide B

Eisuke Sato, Yurika Tanabe, Naoya Nakajima, Akifumi Ohkubo, Kiyotake Suenaga

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

The first total synthesis of biselyngbyolide B, an 18-membered macrolide, was achieved. The 18-membered ring structure was constructed by esterification using the Shiina reagent and an intramolecular Stille coupling reaction.

Original languageEnglish
Pages (from-to)2047-2049
Number of pages3
JournalOrganic Letters
Volume18
Issue number9
DOIs
Publication statusPublished - 2016 May 6

ASJC Scopus subject areas

  • Organic Chemistry
  • Physical and Theoretical Chemistry
  • Biochemistry

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  • Cite this

    Sato, E., Tanabe, Y., Nakajima, N., Ohkubo, A., & Suenaga, K. (2016). Total Synthesis of Biselyngbyolide B. Organic Letters, 18(9), 2047-2049. https://doi.org/10.1021/acs.orglett.6b00660