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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:
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.
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页码:12386 / 12396
页数:11
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