About: Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents

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scientific article published on 01 January 2006

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 2006 (uk) article scientifique (publié 2006) (fr) im Jahr 2006 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 2006 (ast) artikull shkencor i botuar më 01 janar 2006 (sq) scientific article published on 01 January 2006 (en)
publication date	wds:Q82628371-C0854AFC-048E-47D6-87DE-5EB18D197EF2
publication date	2006-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q82628371-00C9C174-55C3-4E39-ABD3-842AA302CB44 wds:Q82628371-03814F92-0C78-49B9-91CD-3B1B4B5450BA wds:Q82628371-170F60BD-2D8D-4A1B-81CB-1EF3E9A187DC wds:Q82628371-431A6B62-6EE5-4528-B27E-5CEA03C8C92C wds:Q82628371-45E0FC9C-B3F0-4BF3-8107-6A9C24D04C07 wds:Q82628371-57CB3367-8FA7-4F79-98E9-5496EA71F6AB wds:Q82628371-5DD6AC33-8993-4232-B19F-ED34E62522C6 wds:Q82628371-5EC8DD19-82EE-45FA-8AEA-A27E06D9156F wds:Q82628371-71D68D74-66EF-4032-91F4-0D8F7AE3718A wds:Q82628371-7DBAA5DB-1F63-4308-AE4F-0A6B6375EEA1 wds:Q82628371-7E324A0A-8F04-4A26-828D-A478157BF438 wds:Q82628371-8290C280-AA0C-4744-BC19-6ED21B15FED7 wds:Q82628371-832EE8FE-21DF-4058-9E56-17CDDB2AEC11 wds:Q82628371-89755469-B3D6-4685-B8D4-BD6940C11856 wds:Q82628371-89913FA9-8357-48F7-BFF1-4D74D0840885 wds:Q82628371-91FF23D0-3972-4E61-9082-67801778D39A wds:Q82628371-955F15EC-C8AA-4812-8EEA-7D8480E55F47 wds:Q82628371-9FD97603-6C18-426B-A886-D38D3AAC9BAE wds:Q82628371-AC8B98A0-F7D3-421C-ACB6-7BD33BEE664A wds:Q82628371-B47EF7E0-AF2A-4BE8-89F4-ED7DCA0C9C70 wds:Q82628371-B58E3D34-49E6-4BDC-A4E6-A75B24E1E41D wds:Q82628371-E914D1F6-3E6D-4689-89A8-32EAB60984A6 wds:Q82628371-EE28A8F5-CB58-4D17-8AD7-5C681529E281 wds:Q82628371-F2CB31AC-0CAD-4CA2-9B1F-642B01927330 wds:Q82628371-F7B38AD0-97E5-4042-971F-5B68DBEC98EA wds:Q82628371-FAB68761-DA71-421E-9272-2EA351909690
cites work	Enantioselective preparation of beta,beta-disubstituted alpha-methylenepropionates by MAO promotion of the zinc Schlenk equilibrium Recent progress in asymmetric allylic substitutions catalyzed by chiral copper complexes. An iterative catalytic route to enantiopure deoxypropionate subunits: asymmetric conjugate addition of grignard reagents to alpha,beta-unsaturated thioesters. Phosphoramidites: marvellous ligands in catalytic asymmetric conjugate addition Solvias Josiphos Ligands: From Discovery to Technical Applications Ferrocenyl Ligands with Two Phosphanyl Substituents in the alpha,varepsilon positions for the Transition Metal Catalyzed Asymmetric Hydrogenation of Functionalized Double Bonds A readily available chiral Ag-based N-heterocyclic carbene complex for use in efficient and highly enantioselective Ru-catalyzed olefin metathesis and Cu-catalyzed allylic alkylation reactions Identification of an Activated Catalyst in the Iridium-Catalyzed Allylic Amination and Etherification. Increased Rates, Scope, and Selectivity Bidentate NHC-based chiral ligands for efficient Cu-catalyzed enantioselective allylic alkylations: structure and activity of an air-stable chiral Cu complex Cu-catalyzed asymmetric allylic alkylations of aromatic and aliphatic phosphates with alkylzinc reagents. An effective method for enantioselective synthesis of tertiary and quaternary carbons Chiral Phosphanodihydrooxazoles in Asymmetric Catalysis: Tungsten-Catalyzed Allylic Substitution Asymmetric catalysis of planar-chiral cyclopentadienylruthenium complexes in allylic amination and alkylation Molybdenum-catalyzed asymmetric allylic alkylations A highly effective phosphoramidite ligand for asymmetric allylic substitution Enantioselective Synthesis of α-Alkyl-β,γ-unsaturated Esters through Efficient Cu-Catalyzed Allylic Alkylations Catalytic enantioselective synthesis of quaternary all-carbon stereogenic centers. Preparation of alpha,alpha'-disubstituted beta,gamma-unsaturated esters through Cu-catalyzed asymmetric allylic alkylations High enantioselectivity in rhodium-catalyzed allylic alkylation of 1-substituted 2-propenyl acetates. Copper-catalyzed asymmetric conjugate addition of Grignard reagents to cyclic enones Copper-catalyzed enantioselective conjugate addition of grignard reagents to acyclic enones A Catalytic and Enantioselective Desymmetrization of meso Cyclic Allylic Bisdiethylphosphates with Organozinc Reagents Organocopper for the craftsman cunning at his trade Copper-catalyzed enantioselective conjugate addition of Grignard reagents to alpha,beta-unsaturated esters Copper(I)-Catalyzed Enantioselective Substitution of Allyl Chlorides with Diorganozinc Compounds Regio- and enantioselective iridium-catalyzed allylic alkylation with in situ activated P,C-chelate complexes Cross-metathesis reaction. Generation of highly functionalized olefins from unsaturated alcohols Enantioselective copper-catalyzed allylic alkylation with dialkylzincs using phosphoramidite ligands
author name string	wds:Q82628371-7F8D86D5-6E41-44EF-B518-480E961A454C wds:Q82628371-CEC8FFFA-03BB-4166-B523-BFB8374191FF
author name string	Adriaan J Minnaard Anthoni W van Zijl
rdfs:label	Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (en) Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (nl) Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (sq)
skos:prefLabel	Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (en) Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (nl) Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (sq)
name	Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (en) Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (nl) Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (sq)
author	wds:Q82628371-A4057C6B-B10B-4B28-8F3B-F7EDAE2A65E4 wds:Q82628371-B39E0816-7FB5-477D-A273-8703177848F6
author	Ben Feringa Fernando López
title	wds:Q82628371-ABAFE10E-B634-421A-927C-683C0672EA30
title	Highly enantioselective Cu-catalysed allylic substitutions with Grignard reagents (en)
page(s)	wds:Q82628371-EF265772-50F5-4CF5-B5E6-FACB8BF78601
page(s)	409-411
instance of	wds:Q82628371-BEB9EAE1-2435-409E-B49D-E79A49854FD2
instance of	scholarly article
main subject	wds:Q82628371-6E8D94CC-233C-49C3-A941-D1A8299093C7
main subject	enantioselectivity
PubMed ID	wds:Q82628371-BD668EF8-BA54-4180-B2DC-92F05D1F1137
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16493816
PubMed ID	16493816
published in	wds:Q82628371-D10268DE-E035-461C-A421-63E248B643DF
published in	Chemical Communications
issue	wds:Q82628371-D7DDF1EB-BF65-4345-B301-F40F0B125221
issue	4
DOI	wds:Q82628371-CC4AA7E3-970F-4954-94C1-AAE510F25A5B
DOI	http://dx.doi.org/10.1039/B513887F
DOI	10.1039/B513887F
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q82628371
is cites work of	Catalytic asymmetric conjugate addition and allylic alkylation with Grignard reagents Copper-catalyzed enantioselective allyl-allyl cross-coupling

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