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可见光催化下α-氨基酸与偕二氟烯烃的脱羧单氟烯基化反应

Visible light photocatalytic decarboxylative monofluoroalkenylation of α-amino acids with gem-difluoroalkenes.

作者信息

Li Jingjing, Lefebvre Quentin, Yang Haijun, Zhao Yufen, Fu Hua

机构信息

Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing 100084, P. R. China.

出版信息

Chem Commun (Camb). 2017 Sep 14;53(74):10299-10302. doi: 10.1039/c7cc05758j.

Abstract

α-Amino acids are among the most common biologically active molecules in nature, and their functionalization has attracted much attention. In this communication, a novel, efficient and general visible-light photocatalytic decarboxylative monofluoroalkenylation of N-protected α-amino acids with gem-difluoroalkenes is reported, affording the corresponding α-amino monofluoroalkenes which might find applications in medical chemistry and materials science. The reaction proceeded at room temperature with high efficiency and tolerance of various functional groups.

摘要

α-氨基酸是自然界中最常见的生物活性分子之一,其官能团化备受关注。在此通讯中,报道了一种新型、高效且通用的可见光光催化N-保护的α-氨基酸与偕二氟烯烃的脱羧单氟烯基化反应,得到相应的α-氨基单氟烯烃,这些产物可能在药物化学和材料科学中得到应用。该反应在室温下高效进行,对各种官能团具有耐受性。

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