About: Copper-Catalyzed Cross-Coupling of Nonactivated Secondary Alkyl Halides and Tosylates with Secondary Alkyl Grignard Reagents

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scholarly article by Chu-Ting Yang et al published 26 June 2012 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2012 (fr) наукова стаття, опублікована в червні 2012 (uk) im Juni 2012 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Chu-Ting Yang et al published 26 June 2012 in Journal of the American Chemical Society (en)
publication date	wds:Q57256633-8834E3E1-CFA2-4F9C-827D-D1AF4477A043
publication date	2012-06-26 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57256633-FD51DF4C-BF1D-40E1-A70C-3FD069020CAA
language of work or name	English
author name string	wds:Q57256633-0709FD3D-4844-4EA1-BCDE-2FE5CA821776 wds:Q57256633-3CF1BDE0-A6AB-4A9A-8B63-5A4F0C11505F wds:Q57256633-86FFA1B1-210D-4847-AA84-403BFA3CF246 wds:Q57256633-A8F587ED-C02D-49BA-A1D1-3C7986E9277B wds:Q57256633-B5C498B5-6330-4E11-9F1C-ED17D0AFA401 wds:Q57256633-EFBCADBC-B28D-4836-9597-136F2F38CA57 wds:Q57256633-FF938B41-F573-438D-9807-C961F9CA596C
author name string	Lei Liu Jun Liang Xiao-Yu Lu Chu-Ting Yang Huan-Huan Chen Jing-Hui Liu Zhen-Qi Zhang
rdfs:label	Copper-Catalyzed Cross-Coupling of Nonactivated Secondary Alkyl Halides and Tosylates with Secondary Alkyl Grignard Reagents (en) Copper-Catalyzed Cross-Coupling of Nonactivated Secondary Alkyl Halides and Tosylates with Secondary Alkyl Grignard Reagents (nl)
skos:prefLabel	Copper-Catalyzed Cross-Coupling of Nonactivated Secondary Alkyl Halides and Tosylates with Secondary Alkyl Grignard Reagents (en) Copper-Catalyzed Cross-Coupling of Nonactivated Secondary Alkyl Halides and Tosylates with Secondary Alkyl Grignard Reagents (nl)
name	Copper-Catalyzed Cross-Coupling of Nonactivated Secondary Alkyl Halides and Tosylates with Secondary Alkyl Grignard Reagents (en) Copper-Catalyzed Cross-Coupling of Nonactivated Secondary Alkyl Halides and Tosylates with Secondary Alkyl Grignard Reagents (nl)
title	wds:Q57256633-6F37DCEF-A5CA-4040-A196-4D6706A5268A
title	Copper-Catalyzed Cross-Coupling of Nonactivated Secondary Alkyl Halides and Tosylates with Secondary Alkyl Grignard Reagents (en)
page(s)	wds:Q57256633-DA11927A-A640-4819-B8E6-75D6D0860D3B
page(s)	11124-11127
instance of	wds:Q57256633-1B89F939-F6E5-401D-BD1F-D67714502329
instance of	scholarly article
main subject	wds:Q57256633-5633D245-9BE5-4E7F-9BC9-225515BB1861
main subject	copper
PubMed ID	wds:Q57256633-4329ADE2-A255-4A24-AADF-E024256B4AE3
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22734716
PubMed ID	22734716
published in	wds:Q57256633-886C7145-112E-4110-BFF6-BD3F8B968090
published in	Journal of the American Chemical Society
issue	wds:Q57256633-A9941447-C3FB-4AA9-895E-E60555E8A4EA
volume	wds:Q57256633-6C4C693E-31DA-4E96-8370-78635DD0862E
issue	27
volume	134
DOI	wds:Q57256633-4C5FCAF1-0C58-4A1A-A409-AA3AB935C33C
DOI	http://dx.doi.org/10.1021/JA304848N
DOI	10.1021/JA304848N
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57256633
is cites work of	Copper-catalyzed regioselective fluorination of allylic halides Highly Efficient, Convergent, and Enantioselective Synthesis of Phthioceranic Acid. sp3-sp3 Coupling reactions in the synthesis of natural products and biologically active molecules Ligand-Controlled Regiodivergent Copper-Catalyzed Alkylboration of Alkenes. Total synthesis of the anti-inflammatory and pro-resolving lipid mediator MaR1n-3 DPA utilizing an sp(3) -sp(3) Negishi cross-coupling reaction. Catalytic enantioselective cross-couplings of secondary alkyl electrophiles with secondary alkylmetal nucleophiles: Negishi reactions of racemic benzylic bromides with achiral alkylzinc reagents Copper-catalysed cross-coupling: an untapped potential Cobalt-Catalyzed Carbonylative Cross-Coupling of Alkyl Tosylates and Dienes: Stereospecific Synthesis of Dienones at Low Pressure. Nickel-Catalyzed Asymmetric Kumada Cross-Coupling of Symmetric Cyclic Sulfates Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (-)-Deschloromytilipin A and (-)-Danicalipin A. Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C-C Bonds Harnessing Alkyl Amines as Electrophiles for Nickel-Catalyzed Cross Couplings via C-N Bond Activation. Copper-catalyzed cross-coupling reactions of epoxides with gem-diborylmethane: access to γ-hydroxyl boronic esters. Nickel-Catalyzed Reductive Allylation of Tertiary Alkyl Halides with Allylic Carbonates. Ni/Co-Catalyzed Homo-Coupling of Alkyl Tosylates Metallaphotoredox-Catalyzed Cross-Electrophile Csp3-Csp3 Coupling of Aliphatic Bromides Iron-catalyzed cross-coupling of unactivated secondary alkyl thio ethers and sulfones with aryl Grignard reagents. Formation of C(sp(3) )-C(sp(3) ) Bonds through Nickel-Catalyzed Decarboxylative Olefin Hydroalkylation Reactions Evidence of Cu(I)/Cu(II) Redox Process by X-ray Absorption and EPR Spectroscopy: Direct Synthesis of Dihydrofurans from β-Ketocarbonyl Derivatives and Olefins. Copper-catalyzed arylation of alkyl halides with arylaluminum reagents Copper-catalysed cross-coupling of arylzirconium reagents with aryl and heteroaryl iodides Copper-Catalyzed Coupling of Triaryl- and Trialkylindium Reagents with Aryl Iodides and Bromides through Consecutive Transmetalations Control of Vicinal Stereocenters through Nickel-Catalyzed Alkyl-Alkyl Cross-Coupling. Catalytic enantioselective synthesis of chiral organic compounds of ultra-high purity of >99% ee N-Heterocyclic carbene copper-catalyzed direct alkylation of terminal alkynes with non-activated alkyl triflates. A Structure-Activity Study of Nickel NNN Pincer Complexes for Alkyl-AlkylKumadaandSuzuki-MiyauraCoupling Reactions Catalyst-controlled doubly enantioconvergent coupling of racemic alkyl nucleophiles and electrophiles
is cites work of	wds:Q64253186-7FCC6F50-E32F-4925-A7BD-D12F436451CD wds:Q44295386-003748D3-1EFD-4B4E-9C76-3DF4000D0AF9 wds:Q41205931-F880BC69-DE0B-4BEA-BC7B-333A7F83FD96 wds:Q40378618-B0825F01-6700-41D4-B7EB-5409ACFB17A7 wds:Q43121795-E7047146-7C72-4C68-A4A7-8DF1D6C7CC3E wds:Q42554304-D5340807-F68F-4794-BDE4-3DAFEB08FB2F wds:Q50962098-ADE5366B-C2EE-45C4-9207-E735E1A09324 wds:Q26783903-DA99B90A-B1FD-4658-97A0-695947C037A0 wds:Q34516169-0B951FAC-3561-4C04-82E6-A2F5416EC4EC wds:Q36049587-181B0F89-F5F7-44A4-82EB-E4B037593345 wds:Q37042095-F3FDEA11-CBA1-499D-849C-F5C4A0E965C5 wds:Q38191444-3C0D8B09-4419-40F0-A027-3EB5D37777BB wds:Q37552203-21B2F4CE-FA3D-4C89-820D-F6D35EDFCE46 wds:Q40359517-C090FD64-0C7F-4C95-8487-6686D39370FF wds:Q44113982-D57D380F-BA72-4364-9ED4-704877D1013D wds:Q51666919-6BD04E34-79BF-4C5C-9F12-E5D170D35AD6 wds:Q90275025-D31DB8AC-A7A3-4101-A067-769964647CA0 wds:Q46394752-1F6FC521-EF0C-46D3-A4F6-60D4C98FBF50 wds:Q46776540-E55A52D2-D7A9-460F-8C1B-F54646C47311 wds:Q36328506-DBDC1CB2-A242-4544-848B-ADDF9E2D8B73 wds:Q40310644-5D831621-F3D0-4E24-AD0F-B9EB52678E8B

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