Chemoselective Silylative Reduction of Conjugated Nitriles under Metal-Free Catalytic Conditions: β-Silyl Amines and Enamines.
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Selective Hydrogenation of Nitriles to Primary Amines Catalyzed by a Polysilane/SiO2-Supported Palladium Catalyst under Continuous-Flow ConditionsLate-stage chemoselective functional-group manipulation of bioactive natural products with super-electrophilic silylium ions.B(C6 F5 )3 -Catalyzed Cascade Reduction of Pyridines.Iron-Catalyzed Mild and Selective Hydrogenative Cross-Coupling of Nitriles and Amines To Form Secondary Aldimines.
P2860
Chemoselective Silylative Reduction of Conjugated Nitriles under Metal-Free Catalytic Conditions: β-Silyl Amines and Enamines.
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name
Chemoselective Silylative Redu ...... : β-Silyl Amines and Enamines.
@en
Chemoselective Silylative Redu ...... : β-Silyl Amines and Enamines.
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type
label
Chemoselective Silylative Redu ...... : β-Silyl Amines and Enamines.
@en
Chemoselective Silylative Redu ...... : β-Silyl Amines and Enamines.
@nl
prefLabel
Chemoselective Silylative Redu ...... : β-Silyl Amines and Enamines.
@en
Chemoselective Silylative Redu ...... : β-Silyl Amines and Enamines.
@nl
P2093
P2860
P356
P1476
Chemoselective Silylative Redu ...... s: β-Silyl Amines and Enamines
@en
P2093
Jinseong Jeong
Juhyeon Park
Sehoon Park
Sukbok Chang
Sung-Woo Park
P2860
P304
P356
10.1002/ANIE.201502366
P407
P577
2015-04-23T00:00:00Z