A convenient and general iron-catalyzed reduction of amides to amines.
about
Iron(III) triflimide as a catalytic substitute for gold(I) in hydroaddition reactions to unsaturated carbon-carbon bonds.Rapid and efficient access to secondary arylmethylamines.Preparation of Enantiomerically Pure Perfluorobutanesulfinamide and Its Application to the Asymmetric Synthesis of α-Amino Acids.Highly chemoselective reduction of amides (primary, secondary, tertiary) to alcohols using SmI2/amine/H2O under mild conditions.Chemoselective reduction of carboxamides.Selective reduction of carboxylic acid derivatives by catalytic hydrosilylation.Homogeneous catalysis using iron complexes: recent developments in selective reductions.Platinum-Catalyzed Reduction of DMF by 1,1,3,3-Tetramethyldisiloxane, HMeSi2OSiMe2H: New Intermediates HSiMe2OSiMe2OCH2NMe2 and HSiMe2(OSiMe2)3OCH2NMe2 and Their Further Chemical ReactivityNickel-Catalyzed Reduction of Secondary and Tertiary Amides.Mild deoxygenation of aromatic ketones and aldehydes over Pd/C using polymethylhydrosiloxane as the reducing agent.Iron-catalyzed hydrogenation for the in situ regeneration of an NAD(P)H model: biomimetic reduction of α-keto-/α-iminoesters.A molecularly defined iron-catalyst for the selective hydrogenation of α,β-unsaturated aldehydes.Selective reduction of amides to amines by boronic acid catalyzed hydrosilylation.Disilametallacyclic chemistry for efficient catalysis.A Manganese Pre-Catalyst: Mild Reduction of Amides, Ketones, Aldehydes, and Esters.Chemoselective Reduction of Tertiary Amides to Amines Catalyzed by Triphenylborane.Selective reduction of esters to aldehydes under the catalysis of well-defined NHC-iron complexes.Unexpected selectivity in ruthenium-catalyzed hydrosilylation of primary amides: synthesis of secondary amines.Selective switchable iron-catalyzed hydrosilylation of carboxylic acids.Amine synthesis through mild catalytic hydrosilylation of imines using polymethylhydroxysiloxane and [RuCl2(arene)]2 catalysts.Two-step synthesis of multi-substituted amines by using an N-methoxy group as a reactivity control element.Selective Reductive Removal of Ester and Amide Groups from Arenes and Heteroarenes through Nickel-Catalyzed C-O and C-N Bond Activation.Chemoselective Reduction of Tertiary Amides under Thermal Control: Formation of either Aldehydes or Amines.Highly selective iron-catalyzed synthesis of alkenes by the reduction of alkynes.Catalyst design for iron-promoted reductions: an iron disilyl-dicarbonyl complex bearing weakly coordinating η2-(H-Si) moieties.Catalytic reduction of amides to amines by electrophilic phosphonium cations via FLP hydrosilylation.Towards a general ruthenium-catalyzed hydrogenation of secondary and tertiary amides to amines.
P2860
Q30625533-9094369A-D42B-4505-8377-39B628AD3458Q36153388-3E084E8E-FECC-449C-889A-73EEB69A4DA4Q36600283-572914E1-1C05-42B8-9F85-C7C7A518E81FQ38698790-F238B939-C99B-4610-ABE6-CC81A94202BFQ38989281-CE308006-04E3-473A-A800-2BB0E6ECAE8FQ39741910-C5539F22-5B45-4301-8974-35D00B18AA9BQ39767874-8CBDC48D-D0D4-4F37-B1F1-717132DEDA01Q41513371-64E9FAB3-4ADA-4C58-87E5-B2154BFA7654Q42187326-6249CCBD-28BA-4991-B094-FA2F730F8604Q42425749-1B29AD44-5784-4070-B222-4A1C2B8F6C35Q44281759-510B6734-8738-4AE4-9C78-F2AE4AB873A5Q44568460-A3AC36FD-F432-4819-BD5F-56178D750B99Q44982079-09482262-05F5-40A8-A6E6-412F9E794717Q46352089-5E91190C-0F9E-41EB-938A-88ACE0123003Q48131188-6D1F2ECA-58ED-4A9C-A5BD-56777F866AF2Q48344496-616DF7F5-C21F-4912-AFA3-98E44FB2B3EBQ50478524-7E7D43A6-47E8-469A-B0F8-8EE865348D8EQ50482654-CF269380-224E-406B-9B2C-6DB53BA91582Q50490468-7ED29B33-28B0-42AE-934A-9EDCB980DC65Q50503056-73AE6E07-6077-4B0D-8DCE-FF93437E39D9Q51732375-8635802F-416B-4BC7-A594-65D2FB25957FQ52780841-97FE5A24-B5A3-4CEE-9D3F-97B7D13BB55AQ52882420-BCA48F7E-3C47-40BE-A5BE-E8B687314240Q52895394-A9F5A53D-8862-4FF4-A00C-12C6440DCCFFQ53090752-3EA3DCF6-302D-4165-893F-E65F1720B678Q53567464-ACF27D6E-550C-4246-A8AC-B2A5CED8C561Q55625835-4AF03965-B77E-4DD6-AD49-7EA5EB6276D2
P2860
A convenient and general iron-catalyzed reduction of amides to amines.
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
name
A convenient and general iron-catalyzed reduction of amides to amines.
@ast
A convenient and general iron-catalyzed reduction of amides to amines.
@en
type
label
A convenient and general iron-catalyzed reduction of amides to amines.
@ast
A convenient and general iron-catalyzed reduction of amides to amines.
@en
prefLabel
A convenient and general iron-catalyzed reduction of amides to amines.
@ast
A convenient and general iron-catalyzed reduction of amides to amines.
@en
P2093
P356
P1476
A convenient and general iron-catalyzed reduction of amides to amines.
@en
P2093
Daniele Addis
Kathrin Junge
Shaolin Zhou
Shoubhik Das
P304
P356
10.1002/ANIE.200904677
P407
P577
2009-01-01T00:00:00Z