About: Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation

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About: Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation Goto Sponge Distinct Permalink

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scientific article published on 01 May 2006

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 2006 (uk) artículu científicu espublizáu en mayu de 2006 (ast) scientific article published on 01 May 2006 (en)
publication date	wds:Q83354917-916FBF69-15ED-411D-9D3D-7FC0526962EC
publication date	2006-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q83354917-2864AC7C-C5B9-466A-B7A1-D308F8D16195
language of work or name	English
cites work	wds:Q83354917-8A7ABEE7-E5EF-4249-95B3-107371004FFE
cites work	Isolation and biological activity of a novel cytokine modulator, cytoxazone
author name string	wds:Q83354917-22E5790F-0ABF-4AAE-8E94-C6CB5CEC46D8 wds:Q83354917-2702E5E0-1AC1-4CE0-8673-EBB697BC6D65 wds:Q83354917-5799657A-C982-439A-984D-D08398F67EBA wds:Q83354917-B8DAAF85-DB6C-4759-B6F5-3DA072E598C1 wds:Q83354917-FC15855B-A01F-4068-BA29-416995CE2468
author name string	Lei Guo Hui Jiang Ximin Li Vladimir B Birman Eric W Uffman
rdfs:label	Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation (en) Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation (nl)
skos:prefLabel	Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation (en) Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation (nl)
name	Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation (en) Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation (nl)
title	wds:Q83354917-EDD73225-D1EE-4BFF-8F8E-326CB2F1F0EC
title	Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation (en)
page(s)	wds:Q83354917-E70BBAB8-5DF2-4730-97BD-17D251589924
page(s)	6536-6537
instance of	wds:Q83354917-1F8861C8-4413-4457-A479-5F3D2E87C8CB
instance of	scholarly article
main subject	wds:Q83354917-5C3D9CD5-4F7A-4D4F-A1A6-1B008AF70834
main subject	enantioselectivity
PubMed ID	wds:Q83354917-4A1ED6D9-F46A-40DE-B78B-825C401D3646
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16704235
PubMed ID	16704235
published in	wds:Q83354917-7A78FC7F-E0E6-4F80-A0E9-14F37B1B9CF4
published in	Journal of the American Chemical Society
issue	wds:Q83354917-69C445AF-585E-433F-BA54-167B61A5AF8D
volume	wds:Q83354917-1E0E09AA-EB48-465E-9F50-175F36E58975
issue	20
volume	128
DOI	wds:Q83354917-A9AC6093-256B-4ED6-8BBF-6F8079CFE0CB
DOI	http://dx.doi.org/10.1021/JA061560M
DOI	10.1021/JA061560M
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q83354917
is cites work of	Origin of enantioselectivity in CF3-PIP-catalyzed kinetic resolution of secondary benzylic alcohols Origin of Substituent Effects in Edge-to-Face Aryl-Aryl Interactions Stereoselective synthesis of cyclic ethers via the palladium-catalyzed intramolecular addition of alcohols to phosphono allylic carbonates Peptide-catalyzed kinetic resolution of formamides and thioformamides as an entry to nonracemic amines. Stereodivergent organocatalytic intramolecular Michael addition/lactonization for the asymmetric synthesis of substituted dihydrobenzofurans and tetrahydrofurans. Isothiourea-catalysed enantioselective pyrrolizine synthesis: synthetic and computational studies. 6-exo-trig Michael addition-lactonizations for catalytic enantioselective chromenone synthesis Effects of Methyl Substituents on the Activity and Enantioselectivity of Homobenzotetramisole-Based Catalysts in the Kinetic Resolution of Alcohols Isothiourea-mediated one-pot synthesis of functionalized pyridines. Benzotetramisole-catalyzed dynamic kinetic resolution of azlactones Non-bonding 1,5-S···O interactions govern chemo- and enantioselectivity in isothiourea-catalyzed annulations of benzazoles. Asymmetric Catalysis of the Carbonyl-Amine Condensation: Kinetic Resolution of Primary Amines. Kinetic resolutions of indolines by a nonenzymatic acylation catalyst The Cation-π Interaction in Small-Molecule Catalysis. Asymmetric Isothiourea-Catalysed Formal [3+2] Cycloadditions of Ammonium Enolates with Oxaziridines Kinetic resolution of secondary alcohols using amidine-based catalysts Iridium(I)-Catalyzed Regio- and Enantioselective Allylic Amidation Stereoselective Lewis acid mediated (3+2) cycloadditions of N-H- and N-sulfonylaziridines with heterocumulenes Determination of absolute configuration using kinetic resolution catalysts. Stereoelectronic basis for the kinetic resolution of N-heterocycles with chiral acylating reagents
is cites work of	wds:Q37278618-1D739074-E1B8-48A9-942A-B632C10436C7 wds:Q37711821-31AD0173-36BB-45EF-8C92-165628A8E62C wds:Q24650813-E5E602D8-F166-4074-9C1B-59E77B284D8F wds:Q35937993-B3A6809A-38D2-468A-9933-F0E84FC0A5A8 wds:Q48346252-456F8CFE-7C58-4B88-9B43-ED2FBA240A06 wds:Q33926142-224C2D6D-FCAC-4FD6-8B8F-CB216AC49D63 wds:Q37238421-16C2E4B6-A721-4E9C-B88B-229A5EEC3AF1 wds:Q38872688-2EC5D703-0DA9-4E01-89AA-B28B4C2F781D wds:Q41869386-181AD59C-1241-4E28-8C9F-06F71360A8EB wds:Q41761917-3F1050ED-AB39-4421-9766-96F781E4429B wds:Q35895376-6279EBCA-90EE-457F-8514-5B5BC7E7731F wds:Q33706020-7688DFE5-8D79-4D7F-A65F-51ED34569B5C wds:Q35231108-3E6373A7-14C6-4325-ADD1-E4A8D92456DE wds:Q40948816-CC7CC637-C39E-4207-92E7-1634C1B3CB02 wds:Q35792784-5852771F-EA33-45CB-BAC8-734C608F0E20 wds:Q37343146-F9A387DA-DD77-488D-9840-6B7A326568D7 wds:Q33744327-6D97862D-C4AD-419B-9071-42F511A6E635 wds:Q34015697-5A731E74-9F54-442F-83DE-74DF8FA747D2 wds:Q37649315-F46613C9-0014-4E2F-AED9-E0B05DCB17FB wds:Q42720911-6F81ADF8-1450-40D6-8894-951D77B76238

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