Total synthesis of exigurin: The Ugi reaction in a hypothetical biosynthesis of natural products

Seijiro Hosokawa*, Keisuke Nakanishi, Yutaro Udagawa, Mitsutoshi Maeda, Seiya Sato, Keiji Nakano, Toshiya Masuda, Yoshiyasu Ichikawa

*この研究の対応する著者

研究成果: Article査読

2 被引用数 (Scopus)

抄録

The first total synthesis of a marine natural product, exigurin, has been accomplished in 13 steps starting from (+)-menthone. The key intermediate (-)-10-epi-axisonitrile-3 was prepared by stereoselective intramolecular cyclopropanation followed by a cyclopropane ring opening reaction by the azide anion. The bioinspired Ugi reaction of (-)-10-epi-axisonitrile-3, formaldehyde, sarcosine and methanol successfully constructed the target exigurin in which its terpene and amino acid units were linked through an amide bond.

本文言語English
ページ(範囲)687-693
ページ数7
ジャーナルOrganic and Biomolecular Chemistry
18
4
DOI
出版ステータスPublished - 2020

ASJC Scopus subject areas

  • 生化学
  • 物理化学および理論化学
  • 有機化学

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