about
Strain-Release Heteroatom Functionalization: Development, Scope, and Stereospecificity.Scandium-catalysed intermolecular hydroaminoalkylation of olefins with aliphatic tertiary aminesNickel-Catalyzed N-Alkylation of Acylhydrazines and Arylamines Using Alcohols and Enantioselective Examples.Nickel-Catalyzed Enantioselective Reductive Amination of Ketones with Both Arylamines and Benzhydrazide.One-Pot N-Deprotection and Catalytic Intramolecular Asymmetric Reductive Amination for the Synthesis of Tetrahydroisoquinolines.Direct Asymmetric Reductive Amination for the Synthesis of Chiral β-Arylamines.The biochemical characterization of three imine-reducing enzymes from Streptosporangium roseum DSM43021, Streptomyces turgidiscabies and Paenibacillus elgii.The mechanism of enantioselective ketone reduction with Noyori and Noyori-Ikariya bifunctional catalysts.Identification of Novel Bacterial Members of the Imine Reductase Enzyme Family that Perform Reductive Amination
P2860
Q37678579-474AD1EA-8640-4E87-81DC-ED6570F6AC0FQ42315603-2E7322E6-9F25-4ED3-B07F-F9C2FF319CBDQ47619722-13D5A9C7-5C9B-4391-98B2-EBED2285EA2FQ48090407-5802445B-31B9-498C-A07A-911405BCB57EQ51023665-A702E7DC-2F7C-478E-8626-12215973F643Q51435033-D8F69C0D-486B-4587-B78A-C969DD2A8270Q53586959-C3BBFC01-72DD-411C-8473-174DD195E5B4Q53624482-79704C0A-C3B1-47C1-8DEF-4271595EFE09Q58048458-1EF96F54-433E-4E08-830F-8C61A76E59D5
P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Asymmetric reductive amination.
@en
type
label
Asymmetric reductive amination.
@en
prefLabel
Asymmetric reductive amination.
@en
P356
P1476
Asymmetric reductive amination
@en
P2093
Jianliang Xiao
P2888
P304
P356
10.1007/128_2013_484
P50
P577
2014-01-01T00:00:00Z