A Boron-Nitrogen Double Transborylation Strategy for Borane-Catalyzed Hydroboration of Nitriles

被引:13
|
作者
Pradhan, Subham [1 ]
Sankar, Raman Vijaya [1 ]
Gunanathan, Chidambaram [1 ]
机构
[1] OCC Homi Bhabha Natl Inst, Natl Inst Sci Educ & Res NISER, Sch Chem Sci, Bhubaneswar 752050, India
来源
JOURNAL OF ORGANIC CHEMISTRY | 2022年 / 87卷 / 18期
关键词
MAIN-GROUP ELEMENTS; PRIMARY AMINES; SELECTIVE HYDROGENATION; REDUCTION; BOND; AMIDES; HYDROSILYLATION; PERSPECTIVE; ALCOHOLS; KINETICS;
D O I
10.1021/acs.joc.2c01655
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Organoborane-catalyzed hydroboration of nitriles provides N,N-diborylamines, which act as efficient synthons for the synthesis of primary amines and secondary amides. Known nitrile hydroboration methods are dominated by metal catalysis. Simple and metal-free hydroboration of nitriles using diborane [H-B-9-BBN](2) as a catalyst and pinacolborane as a turnover reagent is reported. The reaction of monomeric H-B-9-BBN with nitriles leads to the hydrido-bridged diborylimine intermediate; a subsequent sequential double hydroboration-transborylation pathway involving B-N/B-H sigma bond metathesis is proposed.
引用
收藏
页码:12386 / 12396
页数:11
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