About: Catalytic Asymmetric Reductive Amination of α-Branched Ketones

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scholarly article by Vijay N. Wakchaure et al published 20 May 2010 in Angewandte Chemie International Edition

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 2010 (uk) im Mai 2010 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Vijay N. Wakchaure et al published 20 May 2010 in Angewandte Chemie International Edition (en)
publication date	wds:Q58173040-08B5914A-52B1-4DFE-9D28-E2BB8FB0877B
publication date	2010-05-20 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58173040-8D1F14F8-60D4-46CA-A7C4-80663E3CFC32
language of work or name	English
cites work	wds:Q58173040-101A9CA6-5C00-4339-BC66-CFD4E0598911 wds:Q58173040-27D3526F-2C31-476D-AC67-40949BD56C06 wds:Q58173040-2CD249ED-49D1-4852-A1EA-1FF95A128369 wds:Q58173040-2E8875F4-04A3-459F-B11A-A1A4010AF483 wds:Q58173040-33279EB8-DFCC-41FB-849A-EC9A33AEA9AD wds:Q58173040-36D42513-45AA-4B6D-9653-14A14CBC4DE9 wds:Q58173040-386C0CC7-5583-47F1-AFE4-FBC3C6179BB5 wds:Q58173040-412F2748-7B02-4685-BC59-6758073CB344 wds:Q58173040-43DEC987-0C5D-41A6-8F60-FDCE606F264F wds:Q58173040-463D8011-7C80-40BC-887D-DE3D8046FDD4 wds:Q58173040-5C00CC4D-A50D-4BF8-B5BF-AE38843BBB66 wds:Q58173040-625FA688-416F-4C6A-AF20-3048E553408A wds:Q58173040-6BB0BA27-7D76-47AB-B2E3-9948EB37D7EE wds:Q58173040-727622F7-27D2-4E7B-A832-E7867798B045 wds:Q58173040-7F383DDF-0272-453E-BF08-349527C1CD61 wds:Q58173040-8B389000-2A5B-4F66-905F-736703CDA7A1 wds:Q58173040-8BB0B963-31B2-434A-AFF3-857C62113104 wds:Q58173040-9ABF63FB-EA8B-4145-B639-C916A9FF7A30 wds:Q58173040-B6CE5F48-F122-4ACF-88E8-FAF74E479ACA wds:Q58173040-BB6064E6-88AF-49D8-A89B-00446FEC9236 wds:Q58173040-BE13B6C0-A3A9-4A99-9087-7C8A9948D8A1 wds:Q58173040-BE8B2740-ED45-4386-8A1D-B9791856D9F9 wds:Q58173040-C85E9068-0872-417F-9E11-CC42139E6278 wds:Q58173040-CEEC3AFE-AF53-4ECB-B9E6-B53AEB05DFC5 wds:Q58173040-CFC6191D-55EF-45C5-90BF-F98A6BAE86F1 wds:Q58173040-D0345CF1-99BF-4B64-9A67-949C02A65F17 wds:Q58173040-D524BF85-E200-4AA0-9109-E504FA8C3AC8 wds:Q58173040-D71F5005-4518-42A6-AAE7-5F4B3C46CABC wds:Q58173040-D7AC8CAF-00E7-465C-9FFD-7177AD8E2314 wds:Q58173040-DCA8B88E-E705-4A56-A33B-50D4667B4BCE wds:Q58173040-DF68604C-E2B2-4466-9F96-164F9EAA8D2D wds:Q58173040-E1DCE8BC-5C7C-4C36-9222-30FDB4CA5E0A wds:Q58173040-E49293FB-B95A-414E-A7B3-149155D894D9 wds:Q58173040-E5DC26A5-1067-4C1F-827A-4858C6490971 wds:Q58173040-EBF9812A-C6A8-4794-9757-FE79FBBE9BCD wds:Q58173040-EF4AD75A-C6EA-42F8-833D-E2D0AA0BB9B3 wds:Q58173040-FC5EF48D-9278-4BA3-8EEC-F86C973101BC
cites work	Stronger Brønsted acids Theoretical Study of the Mechanism of Hantzsch Ester Hydrogenation of Imines Catalyzed by Chiral BINOL-Phosphoric Acids Stereoselective hydrogenation via dynamic kinetic resolution Design and synthesis of 4-substituted-8-(2-phenyl-cyclohexyl)-2,8-diaza-spiro[4.5]decan-1-one as a novel class of GlyT1 inhibitors: achieving selectivity against the mu opioid and nociceptin/orphanin FQ peptide (NOP) receptors Discovery of N-(2-hydroxy-2-aryl-cyclohexyl) substituted spiropiperidines as GlyT1 antagonists with improved pharmacological profile Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation. Enantioselective Mannich-type reaction catalyzed by a chiral Brønsted acid Enantioselective organocatalytic reductive amination Asymmetric reduction of ketimines with trichlorosilane employing an imidazole derived organocatalyst Enantioselective catalytic reduction of ketoimines with trichlorosilane promoted by readily available chiral Lewis bases. A highly enantioselective organocatalytic method for reduction of aromatic N-alkyl ketimines Asymmetric organocatalytic reductions mediated by dihydropyridines. Catalytic asymmetric reductive amination of aldehydes via dynamic kinetic resolution Chiral phosphoric acids: powerful organocatalysts for asymmetric addition reactions to imines Discovery of CC chemokine receptor-3 (CCR3) antagonists with picomolar potency. A powerful Brønsted acid catalyst for the organocatalytic asymmetric transfer hydrogenation of imines Binaphthol-derived phosphoric acid as a versatile catalyst for enantioselective carbon-carbon bond forming reactions Recent developments in asymmetric transfer hydrogenation with Hantzsch esters: a biomimetic approach Highly enantioselective hydrogenation of enamides catalyzed by chiral phosphoric acids Enantioselective 1,3-dipolar cycloaddition of nitrones with ethyl vinyl ether: the difference between Brønsted and Lewis acid catalysis Benzothiazoline: highly efficient reducing agent for the enantioselective organocatalytic transfer hydrogenation of ketimines Ru-catalyzed asymmetric hydrogenation of racemic aldehydes via dynamic kinetic resolution: efficient synthesis of optically active primary alcohols A one-pot process for the enantioselective synthesis of amines via reductive amination under transfer hydrogenation conditions Highly Enantioselective Hydrogen‐Transfer Reductive Amination: Catalytic Asymmetric Synthesis of Primary Amines Chiral Brønsted Acid Catalyzed Enantioselective Friedel–Crafts Reaction of Indoles and α-Aryl Enamides: Construction of Quaternary Carbon Atoms Highly Enantioselective Reductive Amination of Simple Aryl Ketones Catalyzed by Ir−f-Binaphane in the Presence of Titanium(IV) Isopropoxide and Iodine The First Highly Enantioselective Homogeneously Catalyzed Asymmetric Reductive Amination: Synthesis of α-N-Benzylamino Acids Enantioselective Brønsted Acid Catalyzed Transfer Hydrogenation: Organocatalytic Reduction of Imines SAR studies on a novel series of human cytomegalovirus primase inhibitors Discovery of N-(2-aryl-cyclohexyl) substituted spiropiperidines as a novel class of GlyT1 inhibitors Chiral Brønsted acid-catalyzed direct asymmetric Mannich reaction A vaulted biaryl phosphoric acid-catalyzed reduction of alpha-imino esters: the highly enantioselective preparation of alpha-amino esters. Role of noncovalent interactions in the enantioselective reduction of aromatic ketimines with trichlorosilane A highly enantioselective lewis basic organocatalyst for reduction of N-aryl imines with unprecedented substrate spectrum Dynamic kinetic resolution in the asymmetric synthesis of beta-amino acids by organocatalytic reduction of enamines with trichlorosilane QSAR for anti-RNA-virus activity, synthesis, and assay of anti-RSV carbonucleosides given a unified representation of spectral moments, quadratic, and topologic indices. Catalytic asymmetric hydrogenation of aldehydes
author name string	wds:Q58173040-9CB9A061-7971-411F-8264-4E79A19C714F wds:Q58173040-DAA67ADD-5416-462E-996B-FC00DC65BAD7
author name string	Sebastian Hoffmann Vijay N. Wakchaure
rdfs:label	Catalytic Asymmetric Reductive Amination of α-Branched Ketones (en) Catalytic Asymmetric Reductive Amination of α-Branched Ketones (nl)
skos:prefLabel	Catalytic Asymmetric Reductive Amination of α-Branched Ketones (en) Catalytic Asymmetric Reductive Amination of α-Branched Ketones (nl)
name	Catalytic Asymmetric Reductive Amination of α-Branched Ketones (en) Catalytic Asymmetric Reductive Amination of α-Branched Ketones (nl)
author	wds:Q58173040-36664B88-03D6-44EC-A3FE-D5C451876A1E wds:Q58173040-E4DDDD78-C013-4774-BD59-8DADA0F5F9A1
author	Benjamin List Jian Zhou
title	wds:Q58173040-F7630348-9AB2-460C-979A-7DDA57438586
title	Catalytic Asymmetric Reductive Amination of α-Branched Ketones (en)
page(s)	wds:Q58173040-AB3DBE9B-1821-40D2-AE2C-D8DFB268FF15

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