Copper-catalyzed enantioselective cyanation of benzylic C-H bonds via radical relay
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摘要:
Direct methods that enable stereoselective functionalization of C(sp3)-H bonds could facilitate efficient preparation of therapeutics and agrochemicals,and shall have a major effect on the discovery and development of new pharmaceuticals.Although the transformations through C(sp2)-H bond cleavage have been significantly developed in the past decades,the direct C(sp3)-H functionalization,especially the asymmetric transformation is still a big challenge.