Alternatives to Organoboron Reagents in Rhodium-Catalyzed Conjugate Additions

被引:50
作者
Hargrave, Jonathan D. [1 ]
Allen, Joseph C. [1 ]
Frost, Christopher G. [1 ]
机构
[1] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
关键词
catalysis; conjugate addition; organosilicon reagents; organozinc reagents; rhodium; ALPHA; BETA-UNSATURATED CARBONYL-COMPOUNDS; ASYMMETRIC 1,4-ADDITION; ARYLZINC REAGENTS; STEREOSELECTIVE CONSTRUCTION; STEERING LIGANDS; CHIRAL OLEFINS; ACIDS; KETONES; TANDEM; AIR;
D O I
10.1002/asia.200900512
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The rhodium-catalyzed conjugate addition of organoboron reagents to alkene acceptors has emerged as ail important methodology in organic synthesis. The process results in the formation of new carbon-carbon bonds, and in principle, can create new stereocenters at both the cc and P carbon atoms of the acceptor. Other organometallics are known to participate in the key transmetalation to rhodium and are becoming more established in stereo-selective synthesis (notably arylzinc reagents). This Focus Review will describe recent developments in the use of alternative organometallic donors to organoboron reagents in rhodium-catalyzed conjugate addition reactions and their growing applications in synthesis.
引用
收藏
页码:386 / 396
页数:11
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