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Molecular iodine-mediated reaction of 2-(2-phenylethynyl)-Morita-Baylis-Hillman adducts: An easy route to naphthyl ketones and iodo-substituted isochromenes

  • Donala Janreddy
  • , Veerababurao Kavala
  • , Trimurtulu Kotipalli
  • , R. R. Rajawinslin
  • , Chun Wei Kuo
  • , Wen Chang Huang
  • , Ching Fa Yao*
  • *此作品的通信作者

研究成果: 雜誌貢獻期刊論文同行評審

19   !!Link opens in a new tab 引文 斯高帕斯(Scopus)

摘要

The molecular iodine-promoted reaction of 2-(2-phenylethynyl)-Morita-Baylis-Hillman adducts is reported. In the presence of I2, naphthyl ketone derivatives are produced, whereas in the presence of I2/K3PO4, iodo-substituted isochromene derivatives are produced.

原文英語
頁(從 - 到)8247-8256
頁數10
期刊Organic and Biomolecular Chemistry
12
發行號41
DOIs
出版狀態已發佈 - 2014 11月 7

ASJC Scopus subject areas

  • 生物化學
  • 物理與理論化學
  • 有機化學

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