About: The Mechanism of the Stereospecific Intramolecular Arylation of Lithiated Ureas: The Role of Li+ Probed by Electronic Structure Calculations, and by NMR and IR Spectroscopy

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About: The Mechanism of the Stereospecific Intramolecular Arylation of Lithiated Ureas: The Role of Li+ Probed by Electronic Structure Calculations, and by NMR and IR Spectroscopy Goto Sponge NotDistinct Permalink

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description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 2011 (uk) im Dezember 2011 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q59606085-D50CC84A-B843-40C9-BB9F-5D749F3B8A01
publication date	2011-12-06 00:00:00Z (xsd:dateTime)
cites work	wds:Q59606085-1AD711D3-FFD8-42A2-BA01-14FBC3267B7C wds:Q59606085-5B294DCB-3B95-4382-B5DC-1F4CB0C9FE15 wds:Q59606085-686C9FFF-1F32-47E5-A7CD-714AD22D41D0 wds:Q59606085-7C89E96F-6F62-4CDB-B1FD-75A35755FC7F wds:Q59606085-89334489-013F-40D8-98B9-84F5D66DBA1F wds:Q59606085-8C355709-F0F4-4B77-B91A-B0622580D826 wds:Q59606085-944DBC69-4982-4F79-9239-B30688797941 wds:Q59606085-99A500B9-FFAA-4579-B39A-4DE4195D0BDD wds:Q59606085-A16845E9-998E-4E0F-AE34-8126F241960B wds:Q59606085-A477E3CB-432D-4BD1-9849-094CF06501BD wds:Q59606085-ABE9EF2F-6B3A-4592-8953-3E8B153D146D wds:Q59606085-AE934687-B66C-4455-B06E-484D1FC325D1 wds:Q59606085-BEC1A091-9F6E-4026-A83B-D90028A4A184 wds:Q59606085-C8665E79-DA3E-43F9-9628-891F1FEEB5DD wds:Q59606085-E088CBA2-533B-4A2A-8DE6-DDB648697780 wds:Q59606085-E5496BDB-E180-4B1C-A203-411EA605BEA8 wds:Q59606085-F34E88D8-76E5-4D7A-9644-3B4A1EC8B5D2 wds:Q59606085-FD31E275-7D15-44E1-A9C2-8975EF86F2A0
cites work	The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other fun Asymmetric deprotonation of N-boc piperidine: react IR monitoring and mechanistic aspects Tandem beta-alkylation-alpha-arylation of amines by carbolithiation and rearrangement of N-carbamoyl enamines (vinyl ureas). Additions of Organometallic Reagents to C=N Bonds: Reactivity and Selectivity Asymmetric synthesis of tertiary alcohols and alpha-tertiary amines via Cu-catalyzed C-C bond formation to ketones and ketimines Enantiodivergent conversion of chiral secondary alcohols into tertiary alcohols. Synthesis of highly enantioenriched C-tertiary amines from boronic esters: application to the synthesis of igmesine Quaternary centres bearing nitrogen (α-tertiary amines) as products of molecular rearrangements. Pathways for decomposition of THF by organolithiums: the role of HMPA Ab initio modeling of organolithium equilibria N to C aryl migration in lithiated carbamates: alpha-arylation of benzylic alcohols. Synthesis, isolation, and structure of an LDA-THF complex Substituted Diarylmethylamines by Stereospecific Intramolecular Electrophilic Arylation of Lithiated Ureas Sequential double α-arylation of N-allylureas by asymmetric deprotonation and N→C aryl migration. α-Pyridylation of Chiral Amines via Urea Coupling, Lithiation and Rearrangement Synthesis of (-)-(S,S)-clemastine by invertive N --> C aryl migration in a lithiated carbamate Enantioselective synthesis of tertiary thiols by intramolecular arylation of lithiated thiocarbamates Variations in the solid-state, solution and theoretical structures of a laterally deprotonated aromatic tertiary amide
author name string	wds:Q59606085-07056400-355C-4226-A20A-5736A54DB132 wds:Q59606085-09DEB857-CACE-451B-8D75-B029D8E54C73 wds:Q59606085-1982B93E-F049-4AD7-A8BA-AACE3FDD8299 wds:Q59606085-75E50D3B-731A-47FE-B5F2-FA1FECE7910B wds:Q59606085-95C8DA2E-17B0-4C3E-A531-35E1C55ACC79
author name string	Andrew E. H. Wheatley Mark A. Vincent Ian H. Hillier Alison Campbell Smith Damian M. Grainger
rdfs:label	The Mechanism of the Stereospecific Intramolecular Arylation of Lithiated Ureas: The Role of Li+ Probed by Electronic Structure Calculations, and by NMR and IR Spectroscopy (en) The Mechanism of the Stereospecific Intramolecular Arylation of Lithiated Ureas: The Role of Li+ Probed by Electronic Structure Calculations, and by NMR and IR Spectroscopy (nl)
skos:prefLabel	The Mechanism of the Stereospecific Intramolecular Arylation of Lithiated Ureas: The Role of Li+ Probed by Electronic Structure Calculations, and by NMR and IR Spectroscopy (en) The Mechanism of the Stereospecific Intramolecular Arylation of Lithiated Ureas: The Role of Li+ Probed by Electronic Structure Calculations, and by NMR and IR Spectroscopy (nl)
name	The Mechanism of the Stereospecific Intramolecular Arylation of Lithiated Ureas: The Role of Li+ Probed by Electronic Structure Calculations, and by NMR and IR Spectroscopy (en) The Mechanism of the Stereospecific Intramolecular Arylation of Lithiated Ureas: The Role of Li+ Probed by Electronic Structure Calculations, and by NMR and IR Spectroscopy (nl)
author	wds:Q59606085-643AA0AD-9C06-4666-8EFC-1712AEDBAF90
author	Jonathan Clayden
title	wds:Q59606085-EBE476D2-E21D-496E-8728-F2A609E035CB
title	The Mechanism of the Stereospecific Intramolecular Arylation of Lithiated Ureas: The Role of Li+ Probed by Electronic Structure Calculations, and by NMR and IR Spectroscopy (en)
page(s)	wds:Q59606085-63354ED4-67C8-492B-A7B3-1B3725D99D84
page(s)	731-743
instance of	wds:Q59606085-5B439D44-156B-47E4-B1D3-D0554160C6BE
instance of	scholarly article
published in	wds:Q59606085-B6E0BCC2-AFE9-4EEE-8EB8-59E84E61C182
published in	European Journal of Organic Chemistry
issue	wds:Q59606085-DE219168-413D-42BC-A858-C6CC0073A500
volume	wds:Q59606085-590FAD30-5B91-4670-9398-53AA9020C99D
issue	4
volume	2012
DOI	wds:Q59606085-0EB13692-CFA2-45EE-8427-2BFB604BE741
DOI	http://dx.doi.org/10.1002/EJOC.201101475
DOI	10.1002/EJOC.201101475
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59606085
is cites work of	Asymmetric α-arylation of amino acids Lithium Choreography Determines Contrasting Stereochemical Outcomes of Aryl Migrations in Benzylic Carbamates, Ureas and Thiocarbamates
is cites work of	wds:Q57051023-528149F9-ACA2-4E5C-BDE1-0D90217857CB wds:Q59605872-EA79E912-4953-4B43-8B56-666FBE70C932

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