Tuning radical reactivity for selective radical/radical cross-coupling

被引:73
|
作者
Wang, Shengchun [1 ]
Tang, Shan [1 ]
Lei, Aiwen [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, IAS, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Radical/radical cross-coupling; Tuning radical reactivity; Oxidative cross-coupling; Transient radical; BENZYLIC C-H; ENANTIOSELECTIVE CYANATION; PHOTOREDOX CATALYSIS; BOND FORMATION; STRATEGY; IODINE; DIFUNCTIONALIZATION; FUNCTIONALIZATION; POLYMERIZATION; ANTIOXIDANTS;
D O I
10.1016/j.scib.2018.06.004
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Radical/radical cross-coupling represents a straightforward way for the construction of new chemical bonds in theory and has received more and more attention over the past several years. Until now, it is challenging to achieve the selective bond formation between two transient radicals since selective radical cross-coupling usually happens between persistent radical and transient radical. However, the number of persistent radicals is much less than that of transient radicals. These issues limit the application of radical/radical cross-coupling in the construction of new chemical bonds. To solve this, we proposed a novel strategy "tuning radical reactivity" that could tune transient radical into persistent radical. This paper will introduce the concept and recent developments of "tuning radical reactivity". (C) 2018 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.
引用
收藏
页码:1006 / 1009
页数:4
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