Red-light-mediated BartonMcCombie reaction

Akihiro Ogura, Naoki Ichii, Kouhei Shibata, Ken Ichi Takao

研究成果: Article査読

抄録

A red-light-mediated BartonMcCombie reaction is described, in which chlorophyll a is used as a photocatalyst and tris(trimethylsilyl)silane or Hantzsch ester is used as the hydrogen source. The reaction can be performed with a set of easily available equipment and reagents, and a variety of linear and cyclic xanthates could be applied. In contrast to the traditional conditions, the reaction does not involve toxic organotin or an explosive radical initiator. The reaction mechanism was analyzed both by experiments and computation, and it was suggested that the radical chain mechanism initiated by excitation of complex followed by charge transfer is likely to be operative.

本文言語English
ページ(範囲)936-941
ページ数6
ジャーナルBulletin of the Chemical Society of Japan
93
7
DOI
出版ステータスPublished - 2020 7

ASJC Scopus subject areas

  • Chemistry(all)

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