Photoinduced alkylation of diazines with N-(acyloxy)phthalimides in the presence of triethylamine

Itziar Guerrero, Eugene Yew Kun Tan, Yuliang Liu, Lee J. Edwards, Shunsuke Chiba*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

A photochemical protocol for the alkylation of diazines (pyrimidines, pyrazines and pyridazines) with N-(acyloxy)phthalimides has been developed. The process is facilitated in the presence of triethylamine (Et3N) under irradiation with 427-390 nm light, enabling rapid cross-coupling reactions to construct a wide range of alkylated diazines.

Original languageEnglish
JournalSynthesis
DOIs
Publication statusAccepted/In press - 2023
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2023 Georg Thieme Verlag. All rights reserved.

ASJC Scopus Subject Areas

  • Catalysis
  • Organic Chemistry

Keywords

  • diazines
  • electron-donoracceptor (EDA) complexes
  • Minisci-type alkylation
  • N-(acyloxy)phthalimides
  • radicals

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