Unusual influence of the structures of transition metal complexes on catalytic C-S and C-Se bond formation under homogeneous and heterogeneous conditions

被引:211
作者
Beletskaya, Irina P. [1 ]
Ananikov, Valentine P.
机构
[1] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119899, Russia
[2] Russian Acad Sci, Zelinsky Inst Organ Chem, Moscow 119991, Russia
关键词
synthetic methods; homogeneous catalysis; heterogeneous catalysis; selectivity; nanosized catalysts; FREE-RADICAL ADDITION; VINYL SULFIDES; OXIDATIVE ADDITION; TERMINAL ALKYNES; STEREOSELECTIVE-SYNTHESIS; ZEROVALENT PALLADIUM; DIPHENYL DISELENIDE; 1ST EXAMPLE; CARBONYLATIVE LACTONIZATION; REGIOSELECTIVE-SYNTHESIS;
D O I
10.1002/ejoc.200700119
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In the presence of transition metal catalysts, hydrothiolation and hydroselenation reactions, as well as bisthiolation and bisselenation reactions, have been successfully carried out with high selectivities and yields. New transition metal-catalyzed synthetic methods have been developed for the preparation of vinyl sulfides and vinyl selenides of various types. Mechanistic study has revealed that a homogeneous catalytic system based on phosphine complexes of palladium is the best choice for carrying out stereoselective additions of disulfides and diselenides to alkynes. A heterogeneous Ni-catalyzed reaction with a unique self-organized nanostructured catalyst was superior for carrying out regioselective additions of thiols and selenols to alkynes. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
引用
收藏
页码:3431 / 3444
页数:14
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