Visible-Light-Promoted Intramolecular Annulation of 2-Alkynylbiphenyl Compounds to Synthesize 9-Sulfenylphenanthrenes Under Metal-Free and Additive-Free Conditions

Tao Ma, Mixue Bian, Xinxin Lin, Zhao Yang, Xiaobing Yang, Jindian Duan, Ning Zhu, Chengkou Liu, Zheng Fang, Kai Guo

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

A convenient and environmentally friendly visible-light-promoted annulation reaction of 2-alkynylbiphenyls with diaryldisulfide for the synthesis of 9-sulfenylphenanthrenes bearing a sulfur-containing functional group has been developed. This mild and efficient approach was achieved through continuous irradiation with visible light under metal-free and additive-free conditions. A range of 9-sulfenylphenanthrene products were prepared in moderate to good yields with a broad scope and functional group tolerance.

Original languageEnglish
Article numbere202200208
JournalChemPhotoChem
Volume6
Issue number11
DOIs
StatePublished - Nov 2022

Keywords

  • annulation
  • green synthesis
  • intramolecular cyclization
  • phenanthrenes
  • visible light

Fingerprint

Dive into the research topics of 'Visible-Light-Promoted Intramolecular Annulation of 2-Alkynylbiphenyl Compounds to Synthesize 9-Sulfenylphenanthrenes Under Metal-Free and Additive-Free Conditions'. Together they form a unique fingerprint.

Cite this