N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.
about
Pivalophenone imine as a benzonitrile surrogate for directed C-H bond functionalization.Direct Access to N-Unprotected α- and/or β-Tetrasubstituted Amino Acid Esters via Direct Catalytic Mannich-Type Reactions Using N-Unprotected Trifluoromethyl Ketimines.Cobalt-catalyzed directed C-H alkenylation of pivalophenone N-H imine with alkenyl phosphates.A comprehensive overview of directing groups applied in metal-catalysed C-H functionalisation chemistryHydroarylations by cobalt-catalyzed C-H activation
P2860
N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.
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
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2016年学术文章
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2016年學術文章
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2016年學術文章
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name
N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.
@en
N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.
@nl
type
label
N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.
@en
N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.
@nl
prefLabel
N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.
@en
N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.
@nl
P2860
P356
P1476
N-H Imine as a Powerful Directing Group for Cobalt-Catalyzed Olefin Hydroarylation.
@en
P2093
Wengang Xu
P2860
P304
12731-12735
P356
10.1002/ANIE.201605877
P407
P577
2016-09-15T00:00:00Z