About: Enantioselective nitrone cycloadditions of alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes

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About: Enantioselective nitrone cycloadditions of alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes Goto Sponge NotDistinct Permalink

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scientific article published on 01 July 2006

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2006 (fr) наукова стаття, опублікована в липні 2006 (uk) im Juli 2006 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunetu de 2006 (ast) scientific article published on 01 July 2006 (en)
publication date	wds:Q79888830-6A1F625F-32D1-41ED-BEB0-0BE7185FA5DD
publication date	2006-07-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q79888830-25597E7B-DAAA-461D-997D-774F2BBFF7C0 wds:Q79888830-C3807D01-4690-428B-89B8-439CC13B7BFC
author name string	Keith R Fandrick David A Evans
rdfs:label	Enantioselective nitrone cycloadditions of alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes (en) Enantioselective nitrone cycloadditions of alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes (nl)
skos:prefLabel	Enantioselective nitrone cycloadditions of alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes (en) Enantioselective nitrone cycloadditions of alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes (nl)
name	Enantioselective nitrone cycloadditions of alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes (en) Enantioselective nitrone cycloadditions of alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes (nl)
author	wds:Q79888830-7D4AAF45-A7BE-488D-B0DC-651B13E08F89
author	Hyun-Ji Song
title	wds:Q79888830-9F24AF25-F9B7-422A-BFA9-D1518CF60243
title	Enantioselective nitrone cycloadditions of alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes (en)
page(s)	wds:Q79888830-D80A0632-062C-49B7-924B-95EAA8BC9EB8
page(s)	3351-3354
instance of	wds:Q79888830-CC5E0F39-D3F5-4D6F-8023-01BB3F3546A5
instance of	scholarly article
main subject	wds:Q79888830-1274058F-0CFB-45F3-8EA9-D5AECDBC30E2 wds:Q79888830-C74D7795-6E99-4F4C-81DA-5D414244356E
main subject	cycloaddition enantioselectivity
PubMed ID	wds:Q79888830-9EFDC96F-FE5C-43EB-AFD3-2D0607CEA118
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16836403
PubMed ID	16836403
published in	wds:Q79888830-199F2E8F-522C-4868-A403-63A5705C5024
published in	Organic Letters
issue	wds:Q79888830-BD99C2BD-BCDA-49A3-BB30-63D5C7F02173
volume	wds:Q79888830-83DDDC0F-EBAB-49F3-9447-E91709DC940B
issue	15
volume	8
DOI	wds:Q79888830-DE4311D9-F63B-4DFB-8E1B-0E7B2E0D215F
DOI	http://dx.doi.org/10.1021/OL061223I
DOI	10.1021/OL061223I
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q79888830
is cites work of	DNA-based catalytic enantioselective michael reactions in water. Recent advances in the catalytic asymmetric synthesis of beta-amino acids Stereoselective isoxazolidine synthesis via copper-catalyzed alkene aminooxygenation Solvent enhancement of reaction selectivity: a unique property of cationic chiral dirhodium carboxamidates Enantioselective addition of boronates to chromene acetals catalyzed by a chiral Brønsted acid/Lewis acid system. Enantioselective catalytic β-amination through proton-coupled electron transfer followed by stereocontrolled radical-radical coupling Photocatalytic [2 + 2] cycloadditions of enones with cleavable redox auxiliaries Enantioselective Photocatalytic [3 + 2] Cycloadditions of Aryl Cyclopropyl Ketones. Interfacial electronic effects control the reaction selectivity of platinum catalysts. Copper-catalyzed asymmetric conjugate addition of organometallic reagents to extended Michael acceptors Palladium-catalyzed asymmetric allylic alkylation of 2-acylimidazoles as ester enolate equivalents Highly enantioselective catalytic synthesis of functionalized chiral diazoacetoacetates Lewis acid-catalyzed asymmetric reactions of β,γ-unsaturated 2-acyl imidazoles
is cites work of	wds:Q36302536-84E343B8-0072-408B-BF56-37AB6286A2C6 wds:Q42367444-5D1CD47F-5FEC-4EBA-8062-F8E785715D6E wds:Q48044488-C28D92FB-6E35-44B0-AFE8-F8CCBAAC9A47 wds:Q35048170-33AAD224-2D5F-4CA0-9286-409BEA2B85EF wds:Q37737099-FFBB42D9-ABED-45D4-999F-1D47BB87A3EC wds:Q30987408-128AEEF6-A1DC-4805-BAA7-654E1D2327EE wds:Q46926329-78236708-D65D-414B-8C41-4D195CE796E4 wds:Q98196735-C5E2520F-49EE-49AE-BE5C-0EBBD0E02CBC wds:Q24629636-C8A4F466-4068-416F-8081-2C9BBE0B6828 wds:Q26770628-CECD9C0C-4C64-48F5-83A1-9C40A72B52C5 wds:Q41504899-710E1E61-80CC-4856-8341-916721051904 wds:Q34011631-BF2DA8E1-D142-4FDB-B7BF-ACBC3D5BFCC1 wds:Q36008506-31E5029A-86E4-4887-8770-E9BD8C899761

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