Aerobic Copper-Promoted Radical-Type Cleavage of Coordinated Cyanide Anion: Nitrogen Transfer to Aldehydes To Form Nitriles.
about
AgNO3 as nitrogen source for rhodium(iii)-catalyzed synthesis of 2-aryl-2H-benzotriazoles from azobenzenes.Mechanistic Insight Facilitates Discovery of a Mild and Efficient Copper-Catalyzed Dehydration of Primary Amides to Nitriles Using Hydrosilanes.Cu(ii)-Mediated keto C(sp3)-H bond α-acyloxylation of N,N-dialkylamides with aromatic carboxylic acids.tert-Butyl nitrite (TBN) as the N atom source for the synthesis of substituted cinnolines with 2-vinylanilines and a relevant mechanism was studied.Redox reaction between benzyl azides and aryl azides: concerted synthesis of aryl nitriles and anilines.
P2860
Aerobic Copper-Promoted Radical-Type Cleavage of Coordinated Cyanide Anion: Nitrogen Transfer to Aldehydes To Form Nitriles.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
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2016年學術文章
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name
Aerobic Copper-Promoted Radica ...... to Aldehydes To Form Nitriles.
@en
Aerobic Copper-Promoted Radica ...... to Aldehydes To Form Nitriles.
@nl
type
label
Aerobic Copper-Promoted Radica ...... to Aldehydes To Form Nitriles.
@en
Aerobic Copper-Promoted Radica ...... to Aldehydes To Form Nitriles.
@nl
prefLabel
Aerobic Copper-Promoted Radica ...... to Aldehydes To Form Nitriles.
@en
Aerobic Copper-Promoted Radica ...... to Aldehydes To Form Nitriles.
@nl
P2093
P356
P1476
Aerobic Copper-Promoted Radica ...... to Aldehydes To Form Nitriles.
@en
P2093
P304
P356
10.1021/JACS.5B10945
P407
P50
P577
2016-02-23T00:00:00Z