Applications of catalysis in hydroboration of imines, nitriles, and carbodiimides

被引:34
作者
Bazkiaei, Adineh Rezaei [1 ]
Findlater, Michael [2 ]
Gorden, Anne E., V [1 ]
机构
[1] Texas Tech Univ, Dept Chem & Biochem, Lubbock, TX 79409 USA
[2] Univ Calif Merced, Dept Chem & Biochem, Merced, CA 95343 USA
基金
美国国家科学基金会;
关键词
TRANSITION-METAL; SELECTIVE HYDROBORATION; MAGNESIUM CATALYSIS; OXIDATIVE-ADDITION; CARBONYL-COMPOUNDS; HYDROGENATION; ALDEHYDES; COMPLEXES; REACTIVITY; REDUCTION;
D O I
10.1039/d2ob00162d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The catalytic hydroboration of imines, nitriles, and carbodiimides is a powerful method of preparing amines which are key synthetic intermediates in the synthesis of many value-added products. Imine hydroboration has perennially featured in notable reports while nitrile and carbodiimide hydroboration have gained attention recently. Initial developments in catalytic hydroboration of imines and nitriles employed precious metals and typically required harsh reaction conditions. More recent advances have shifted toward the use of base metal and main group element catalysis and milder reaction conditions. In this survey, we review metal and nonmetal catalyzed hydroboration of these unsaturated organic molecules and group them into three distinct categories: precious metals, base metals, and main group catalysts. The TON and TOF of imine hydroboration catalysts are reported and summarized with a brief overview of recent advances in the field. Mechanistic and kinetic studies of some of these protocols are also presented.
引用
收藏
页码:3675 / 3702
页数:28
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