4.7 Article

Visible Light-Induced Difunctionalization of Alkynes: The Synthesis of Thiazoles and 1,1-Dibromo-1-en-3-ynes

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 84, Issue 23, Pages 15283-15293

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.9b02300

Keywords

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Funding

  1. National Natural Science Foundation of China [21861006, 21861015]
  2. Natural Science Foundation of Guangxi [2018GXNSFBA138050, 2017GXNSFBA198205]
  3. Special Fund for Talents of Guangxi [AD18281028, AD18281035]

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A visible light-induced cascade cyclization of thioamides with alkynes was developed to synthesize 1,3-thiozoles. The sulfur radical generated from thioamide via the single-electron transfer (SET) pathway was promoted by photocatalysis as a key intermediate in this reaction. When bromoalkynes were used as the substrate, the self-coupling products 1,1-dibromo-1-en-3-ynes were obtained in moderate yields, and an energy transfer pathway for this transformation promoted by visible-light photocatalysis was proposed.

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