TaMe3Cl2-catalyzed intermolecular hydroaminoalkylation: a simple complex for enhanced reactivity and expanded substrate scope.
about
Recent advances in catalytic C-N bond formation: a comparison of cascade hydroaminomethylation and reductive amination reactions with the corresponding hydroamidomethylation and reductive amidation reactions.Scandium-catalysed intermolecular hydroaminoalkylation of olefins with aliphatic tertiary aminesPhosphoramidate tantalum complexes for room-temperature C-H functionalization: hydroaminoalkylation catalysis.Intermolecular hydroaminoalkylation of alkenes and dienes using a titanium mono(formamidinate) catalyst.One-Pot Procedure for the Synthesis of 1,5-Benzodiazepines from N-Allyl-2-bromoanilines.Hydroaminoalkylation of Allylsilanes and a One-Pot Procedure for the Synthesis of 1,5-Benzoazasilepines.
P2860
TaMe3Cl2-catalyzed intermolecular hydroaminoalkylation: a simple complex for enhanced reactivity and expanded substrate scope.
description
2013 nî lūn-bûn
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name
TaMe3Cl2-catalyzed intermolecu ...... and expanded substrate scope.
@en
TaMe3Cl2-catalyzed intermolecu ...... and expanded substrate scope.
@nl
type
label
TaMe3Cl2-catalyzed intermolecu ...... and expanded substrate scope.
@en
TaMe3Cl2-catalyzed intermolecu ...... and expanded substrate scope.
@nl
prefLabel
TaMe3Cl2-catalyzed intermolecu ...... and expanded substrate scope.
@en
TaMe3Cl2-catalyzed intermolecu ...... and expanded substrate scope.
@nl
P2093
P2860
P356
P1476
TaMe3Cl2-catalyzed intermolecu ...... and expanded substrate scope.
@en
P2093
Jean-Denys Hamel
Laurel L Schafer
Zhengxing Zhang
P2860
P304
P356
10.1002/CHEM.201300992
P407
P577
2013-05-17T00:00:00Z