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电化学驱动,使用X(CF)X实现(杂)芳烃的钴-碳键介导的直接分子内环化和无环全氟烷基化反应

Electrochemically driven, cobalt-carbon bond-mediated direct intramolecular cyclic and acyclic perfluoroalkylation of (hetero)arenes using X(CF)X.

作者信息

Cui Luxia, Ono Toshikazu, Hossain Md Jakir, Hisaeda Yoshio

机构信息

Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University 744 Motooka Nishi-ku Fukuoka 819-0395 Japan

Center for Molecular Systems (CMS), Kyushu University 744 Motooka Nishi-ku Fukuoka 819-0395 Japan.

出版信息

RSC Adv. 2020 Jun 30;10(42):24862-24866. doi: 10.1039/d0ra05295g. eCollection 2020 Jun 29.

Abstract

A proof-of-concept for the one-step, synthetically challenging cyclic and acyclic perfluoroalkylation of (hetero)arenes driven by the valence change of a vitamin B derivative as a cobalt catalyst in the presence of fluoroalkylating reagents (X(CF)X) is presented. The consecutive formation of cobalt-carbon bonds and generation of fluoroalkyl radicals by homolysis are the key steps for the reaction to proceed.

摘要

本文展示了在氟烷基化试剂(X(CF)X)存在下,由维生素B衍生物作为钴催化剂的价态变化驱动的(杂)芳烃一步合成具有挑战性的环状和非环状全氟烷基化的概念验证。钴-碳键的连续形成和均裂产生氟烷基自由基是反应进行的关键步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d426/9055166/55d4aa9cfe2f/d0ra05295g-s1.jpg

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