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Tandem Vinylogous Aldol and Intramolecular [2 + 2] Cycloaddition toward Benzocyclobutenes by UV Light Photocatalysis.

Hong-Bo TanYing-Shan LiuJia-Ying ZhouMan CaoTong LeiSi-Ying RenChang-Qiu LinYi-Fan YangZhang-Liang HuZhi-Gang XuDian-Yong TangZhong-Zhu ChenXian-You Qu
Published in: Organic letters (2024)
A facile and efficient radical tandem vinylogous aldol and intramolecular [2 + 2] cycloaddition reaction for direct synthesis of cyclobutane-containing benzocyclobutenes (BCBs) under extremely mild conditions without using any photocatalysts is reported. This approach exhibited definite compatibility with functional groups and afforded new BCBs with excellent regioselectivity and high yields. Moreover, detailed mechanism studies were carried out both experimentally and theoretically. The readily accessible, low-cost, and ecofriendly nature of the developed strategy will endow it with attractive applications in organic and medicinal chemistry.
Keyphrases
  • low cost
  • visible light
  • energy transfer
  • quantum dots
  • case control
  • water soluble
  • reduced graphene oxide
  • gold nanoparticles
  • electron transfer