about
Chemoselective reduction of carboxamides.Mild Reductive Functionalization of Amides into N-Sulfonylformamidines.Chemoselective Reduction of Tertiary Amides under Thermal Control: Formation of either Aldehydes or Amines.Mo(CO)6 catalysed chemoselective hydrosilylation of α,β-unsaturated amides for the formation of allylaminesRuthenium-catalyzed tandem-isomerization/asymmetric transfer hydrogenation of allylic alcoholsFacile preparation of pyrimidinediones and thioacrylamides via reductive functionalization of amidesStraightforward α-Amino Nitrile Synthesis Through Mo(CO)6 -Catalyzed Reductive Functionalization of Carboxamides
P50
Q38989281-F3632605-4B7A-41F9-81A9-3B10776F22EAQ41239467-A07B42F8-798B-4DAE-AD5A-190360F2EE41Q52882420-4C1E9837-485E-4C0B-A419-2D5A74CE99BBQ85759219-D643A318-15ED-46AE-BB00-4BFDB1A8B1E5Q85844037-3BA118E1-829E-4667-8A2F-E896BD22EAF9Q88658593-937A33B4-B388-4C2B-A895-E41AEAC567F4Q90801647-19047F03-8C92-4E54-A0C0-45C877DFEB9D
P50
description
investigador
@es
researcher
@en
name
Tove Slagbrand
@en
type
label
Tove Slagbrand
@en
prefLabel
Tove Slagbrand
@en
P31
P496
0000-0003-2013-8093