作为一种战略反应的C-H激活:对4-置换的醇进行enantioselective合成

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Updated: Jul 17, 2026

Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)
06:34

Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)

Published on: June 20, 2014

Huw M L Davies1, James R Manning

  • 1Department of Chemistry, University at Buffalo, The State University of New York, 14260-3000, USA. hdavies@buffalo.edu

Journal of the American Chemical Society
|January 26, 2006
PubMed
概括

这项研究引入了一种新的方法,用于使用催化剂制造4-置换的内醇. 该过程实现了高产量和出色的立体选择性,推进了不对称合成技术.

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