The Stille Reaction, 38 Years Later

被引:342
作者
Cordovilla, Carlos [1 ]
Bartolome, Camino [1 ]
Martinez-Ilarduya, Jesus Ma [1 ]
Espinet, Pablo [1 ]
机构
[1] Univ Valladolid, Fac Ciencias, IU CINQUIMA Quim Inorgan, Valladolid 47071, Spain
关键词
Stille cross-coupling; reaction mechanism; transmetalation; palladium; tin; CROSS-COUPLING REACTIONS; SUPPORTED ORGANOTIN REAGENTS; DENSITY-FUNCTIONAL THEORY; ARYL HALIDES; REDUCTIVE ELIMINATION; OXIDATIVE ADDITION; TRANSMETALATION STEP; ACYL CHLORIDES; STANNYLATED POLYNORBORNENES; PALLADIUM(II) COMPLEXES;
D O I
10.1021/acscatal.5b00448
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The first now-named Stile reaction was published 38 years ago, and the last comprehensive revision of this catalysis was in 2004. Since then, the knowledge of the different steps of the three possible (and sometimes competing) reaction pathways (cyclic, open, and ionic) has been almost completed by synergistic experimental and theoretical studies: the Stille reaction is perhaps the best characterized catalytic process if we consider the number of intermediates that have been detected. This review concentrates on the mechanistic new knowledge and on important aspects such as the revolution with the use of bulky phosphines, the bimetallic alternative of the Stille reaction, the enantioselectivity in Stille and palladium-free Stille processes, the meaning of copper effect, or the possible approaches to make Stille coupling a greener process.
引用
收藏
页码:3040 / 3053
页数:14
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