About: Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts

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About: Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts Goto Sponge NotDistinct Permalink

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scientific article published on January 2008

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2008 (ast) наукова стаття, опублікована в січні 2008 (uk) scientific article published on January 2008 (en) مقالة علمية نشرت في يناير 2008 (ar)
publication date	wds:Q37120806-7E219BFD-BE8C-438C-AF85-0E68ACF533E3
publication date	2008-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37120806-60DFBED1-202B-4CA5-B002-82708D76F3C3
language of work or name	English
cites work	wds:Q37120806-07204ECA-7C2C-4F29-A678-5668D8847D5A wds:Q37120806-138A1B6E-FF3F-46D1-838C-14046D2F76CD wds:Q37120806-153A7C87-D35F-4161-B7E7-70621EB5550A wds:Q37120806-1C749476-1E73-45E7-9D78-3901CAEA4A5B wds:Q37120806-2B5D3861-3090-4E5F-9132-ED4C7641125C wds:Q37120806-2C44CF24-6741-46EA-8DCF-04ED5CF2A810 wds:Q37120806-2EA126EB-EA2C-403B-9A72-8354CD70146F wds:Q37120806-34B67D50-B12A-4738-A11B-C2B9C65F8C4B wds:Q37120806-3920A029-3A08-4EC8-93D1-68F1FFC280B5 wds:Q37120806-4543CED6-B4F5-4890-AAE2-E9388CCFE5A5 wds:Q37120806-49EB9BAF-1E10-4BE1-A065-668A6DE558D3 wds:Q37120806-6D289FDC-BD0D-48D4-9539-A37C86A0161A wds:Q37120806-71995472-D62C-49B0-874C-88BC3AD243F6 wds:Q37120806-7757E143-F780-470F-8CB7-0FECD9C6D4D1 wds:Q37120806-7FFB0749-8C99-42AD-B5C0-765C42E12BCB wds:Q37120806-8664D1F1-2B38-41F5-B11E-7ABCC9F45510 wds:Q37120806-8BB6AF55-3E3B-476D-B119-BDC581284D72 wds:Q37120806-8D465B05-C365-4ADD-B0CC-2EB71724F517 wds:Q37120806-94AFB537-E87D-42E1-8567-AFBD738C48D2 wds:Q37120806-BA10AB0C-DF17-431D-88E6-7BCC2A1DC0C6 wds:Q37120806-BEF42DE8-D97A-48E4-BCAA-991993716B77 wds:Q37120806-C672DDED-53D6-45FC-B6D4-38638F8EAF57 wds:Q37120806-D715016A-7EBE-4E97-8929-CF67B9A12772 wds:Q37120806-E10D162A-F91F-46D9-AB66-0E8B6AE4B11C wds:Q37120806-E4DEE53E-D1C8-4AC7-9FB2-4EAFC05C7761 wds:Q37120806-EC6696E0-457A-4BFA-BA9E-DE74C496A9CE
cites work	Highly enantioselective michael addition of cyclic 1,3-dicarbonyl compounds to alpha,beta-unsaturated ketones Catalytic enantioselective peroxidation of alpha,beta-unsaturated ketones Catalytic asymmetric epoxidation of cyclic enones Organocatalytic asymmetric Friedel-Crafts alkylation of indoles with simple alpha,beta-unsaturated ketones Highly asymmetric Michael addition to alpha,beta-unsaturated ketones catalyzed by 9-amino-9-deoxyepiquinine Readily accessible 9-epi-amino cinchona alkaloid derivatives promote efficient, highly enantioselective additions of aldehydes and ketones to nitroolefins Organocatalytic enantioselective indole alkylations of alpha,beta-unsaturated ketones Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst Iminium catalysis Organocatalytic transfer hydrogenation of cyclic enones Enantioselective organocatalytic amine conjugate addition Asymmetric azidation-cycloaddition with open-chain peptide-based catalysts. A sequential enantioselective route to triazoles. Heterobimetallic catalysis in asymmetric 1,4-addition of O-alkylhydroxylamine to enones Lewis acid-Lewis acid heterobimetallic cooperative catalysis: mechanistic studies and application in enantioselective aza-Michael reaction Enantioselective Synthesis of α,β-Disubstituted-β-amino Acids Highly enantioselective conjugate additions to alpha,beta-unsaturated ketones catalyzed by a (salen)Al complex Chiral Diphenylprolinol TES ether promoted conjugate addition-aldol-dehydration reactions between alpha,beta-unsaturated aldehydes and 2-N-protected amino benzaldehydes. Organocatalytic enantioselective aza-Michael reaction of nitrogen heterocycles and α,β-unsaturated aldehydes Highly enantioselective transfer hydrogenation of alpha,beta-unsaturated ketones Organocatalytic enantioselective aziridination of alpha,beta-unsaturated aldehydes Enantioselective organocatalytic conjugate addition of N heterocycles to alpha,beta-unsaturated aldehydes Organocatalytic asymmetric 5-hydroxyisoxazolidine synthesis: a highly enantioselective route to beta-amino acids Asymmetric aza-Michael reactions catalyzed by cinchona alkaloids Catalytic enantioselective conjugate addition of carbamates Organocatalysis in conjugate amine additions: synthesis of beta-amino acid derivatives Organocatalytic and highly enantioselective direct alpha-amination of aromatic ketones
author name string	wds:Q37120806-00DE73D4-D6E5-45CC-9CFF-8CD9223A2E76 wds:Q37120806-336BC361-AB3C-457C-8196-4BF3D79E26A2
author name string	Li Deng Xiaojie Lu
rdfs:label	Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts (en) Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts (ast) Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts. (nl)
skos:prefLabel	Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts (en) Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts (ast) Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts. (nl)
name	Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts (en) Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts (ast) Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts. (nl)
title	wds:Q37120806-F4261459-232D-4F72-A397-10DCA916B12B
title	Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts (en)
page(s)	wds:Q37120806-509E9D0E-021B-4127-8ACB-E3DF1B51BB09
page(s)	7710-7713
instance of	wds:Q37120806-68D3F477-F8ED-45B6-94DA-EAD8D4781EDF
instance of	scholarly article
PubMed ID	wds:Q37120806-EC08A042-4CE9-423F-B921-6D99EDD73BE7
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18756559
PubMed ID	18756559
published in	wds:Q37120806-4A8636AD-214E-4700-9BAD-15E9CE24C430
published in	Angewandte Chemie International Edition
issue	wds:Q37120806-BB436F42-FD14-4B50-B628-C72F2CAC4410
volume	wds:Q37120806-2A14EF28-B156-492C-9121-4BDA5DB5B8D1
issue	40

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