Chelation-assisted transition metal-catalysed C-H chalcogenylations

被引:78
作者
Ma, Wenbo [1 ]
Kaplaneris, Nikolaos [2 ]
Fang, Xinyue [1 ]
Gu, Linghui [1 ]
Mei, Ruhuai [3 ]
Ackermann, Lutz [2 ]
机构
[1] Chengdu Univ, Sichuan Ind Inst Antibiot, Antibiot Res & Re Evaluat Key Lab Sichuan Prov, Chengdu 610052, Peoples R China
[2] Georg August Univ Goettingen, Inst fuer Organ & Biomol Chem, Tammannstr 2, D-37077 Gottingen, Germany
[3] Chengdu Univ, Coll Pharm & Biol Engn, Chengdu 610106, Peoples R China
关键词
CROSS-COUPLING REACTIONS; LATE-STAGE DIVERSIFICATION; SITE-SELECTIVE ACCESS; DIRECT THIOLATION; BOND FORMATION; C(SP(2))-H BONDS; BENZOIC-ACIDS; EFFICIENT SYNTHESIS; C(SP(3))-H BONDS; DIRECTING GROUPS;
D O I
10.1039/c9qo01497g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The development of convenient and mild chalcogenylation reactions for the preparation of unsymmetrical diaryl sulfides and diaryl selenides has received significant attention in recent years due to their prevalence in natural products, organic molecular syntheses, catalysis, drug candidates and functional materials. In contrast with conventional organic transformations which largely rely on the inherent reactivity of functional groups, transition metal-catalysed direct C-H functionalizations have emerged as a powerful strategy that eliminates prefunctionalised starting materials and thus leads to more atom- and step-economical processes. This review summarizes the recent advances in C-S and C-Se formations via transition metal-catalyzed C-H functionalization utilizing directing groups to control the site-selectivity until autumn 2019. Typical examples are listed and mechanistic aspects are discussed in detail.
引用
收藏
页码:1022 / 1060
页数:39
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