Visible-Light Photocatalysis as an Enabling Tool for the Functionalization of Unactivated C(sp3)-Substrates

被引:73
作者
Roslin, Sara [1 ]
Odell, Luke R. [1 ]
机构
[1] Uppsala Univ, Organ Pharmaceut Chem, Uppsala Biomed Ctr, Dept Med Chem, POB 574, S-75123 Uppsala, Sweden
关键词
Photocatalysis; Photochemistry; Alkyl radicals; Radical reactions; Visible light; Cross-coupling; PHOTOREDOX/NICKEL DUAL CATALYSIS; SINGLE-ELECTRON TRANSMETALATION; BIOMOLECULE-COMPATIBLE CONDITIONS; ALIPHATIC CARBOXYLIC-ACIDS; CARBON-CENTERED RADICALS; H BOND FUNCTIONALIZATION; CROSS-COUPLING REACTIONS; BORYLATED ARYL BROMIDES; NICKEL CATALYSIS; DECARBOXYLATIVE FLUORINATION;
D O I
10.1002/ejoc.201601479
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Over the past decade, visible-light photocatalysis has emerged as one of the brightest and most dynamic fields in modern organic chemistry. By employing a transition-metal- or organic-dye-based photocatalyst in conjunction with a low-energy visible-light source, this synthetic manifold allows the facile generation of radical intermediates that can subsequently be directed through a wide range of transformations. Although initial studies focused largely on the functionalization of stabilized radical intermediates, over the past few years significant efforts have been directed towards the functionalization of challenging unactivated radical precursors. In this review we summarize the recent developments in the use of visible-light photocatalysis for the functionalization of unactivated C(sp(3))-substrates.
引用
收藏
页码:1993 / 2007
页数:15
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