About: On the Nature of the "Copper Effect" in the Stille Cross-Coupling

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scholarly article by Vittorio Farina et al published October 1994 in Journal of Organic Chemistry

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 1994 (uk) article scientifique publié en 1994 (fr) im Oktober 1994 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Vittorio Farina et al published October 1994 in Journal of Organic Chemistry (en)
publication date	wds:Q56482561-849DE951-2479-4DBB-BDCE-C0C6916301DE
publication date	1994-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56482561-25034E86-BD04-4899-875F-9A3570348CDB
language of work or name	English
author name string	wds:Q56482561-4F617161-A308-49B7-9DE3-CCD42DDA05D5 wds:Q56482561-7BA1691A-C17E-43E1-BF0A-A78A89F64933 wds:Q56482561-7CD011C8-63EF-40CB-82E5-415945D150E4 wds:Q56482561-D5FE45AC-DBFB-4DB4-AB38-3D0AD50411EE wds:Q56482561-E1977467-256C-4867-AAC6-AEEC5284CC59
author name string	Suresh Kapadia Bala Krishnan Vittorio Farina Chenjie Wang Lanny S. Liebeskind
rdfs:label	On the Nature of the "Copper Effect" in the Stille Cross-Coupling (en) On the Nature of the "Copper Effect" in the Stille Cross-Coupling (nl)
skos:prefLabel	On the Nature of the "Copper Effect" in the Stille Cross-Coupling (en) On the Nature of the "Copper Effect" in the Stille Cross-Coupling (nl)
name	On the Nature of the "Copper Effect" in the Stille Cross-Coupling (en) On the Nature of the "Copper Effect" in the Stille Cross-Coupling (nl)
title	wds:Q56482561-8882D993-DBD2-43C9-96DB-2F3BD47CA0A0
title	On the Nature of the "Copper Effect" in the Stille Cross-Coupling (en)
page(s)	wds:Q56482561-6CC06692-7B3C-4290-9C92-7EBA10305DB7
page(s)	5905-5911
instance of	wds:Q56482561-849C8CDA-BF86-4AA0-A0A4-10FA4E1A2ECB
instance of	scholarly article
main subject	wds:Q56482561-FCEDF796-F3B7-4603-B8F4-623D17E82DED
main subject	copper
published in	wds:Q56482561-E020D28E-4B87-482C-B4D4-26EFD6C6D7FE
published in	Journal of Organic Chemistry
issue	wds:Q56482561-2E1BED91-DA03-4A46-B0E0-8638CA39B6F3
volume	wds:Q56482561-8BEE7910-81BE-4CC1-A1E3-80C43DA310B2
issue	20
volume	59
DOI	wds:Q56482561-91D7DEE0-5430-40BB-8DA4-271F3412FC89
DOI	http://dx.doi.org/10.1021/JO00099A018
DOI	10.1021/JO00099A018
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56482561
is cites work of	Synthesis and reactivity of an alpha-stannyl beta-silyl enamide Highly functionalized organomagnesium reagents prepared through halogen-metal exchange The total synthesis of (-)-crispatene Synergistic Catalysis: A Powerful Synthetic Strategy for New Reaction Development Synthesis of dibenzothiophenes and related classes of heterocycles by using functionalized dithiocarbamates Coupling of isoprenoid triflates with organoboron nucleophiles: synthesis and biological evaluation of geranylgeranyl diphosphate analogues On the Triple Role of Fluoride Ions in Palladium-Catalyzed Stille Reactions Total synthesis of indole-derived allocolchicine analogues exhibiting strong apoptosis-inducing activity Highly-functionalised difluorinated (hydroxymethyl)conduritol analogues via the Diels-Alder reactions of a difluorinated dienophile Thwarting beta-Hydride Elimination: Capture of the Alkylpalladium Intermediate of an Asymmetric Intramolecular Heck Reaction This research was supported by the National Institutes of Health (grant GM-12389). M.O. thanks the Deutsche Forschungsgemein Thwarting β-Hydride Elimination: Capture of the Alkylpalladium Intermediate of an Asymmetric Intramolecular Heck Reaction Bimetallic catalysis using transition and Group 11 metals: an emerging tool for C-C coupling and other reactions Stille coupling involving bulky groups feasible with gold cocatalyst Copper-free, recoverable dendritic Pd catalysts for the Sonogashira reaction Pd-mediated rapid cross-couplings using [(11) C]methyl iodide: groundbreaking labeling methods in (11) C radiochemistry. Recent advances in heterobimetallic palladium(II)/copper(II) catalyzed domino difunctionalization of carbon-carbon multiple bonds Convergent Total Syntheses of Gambierol and 16-epi-Gambierol and Their Biological Activities Palladium-catalyzed ligand-promoted site-selective cyanomethylation of unactivated C(sp3)-H bonds with acetonitrile Two Enabling Strategies for the Stereoselective Conversion of Internal Alkynes into Trisubstituted Alkenes. Introduction of Aromatic and Heteroaromatic Groups in the 2- and 8-Positions of the Tröger’s Base Core by Suzuki, Stille and Negishi Cross-Coupling Reactions - A Comparative Study The effect of DMSO on the borohydride reduction of a cyclohexanone: A formal enantioselective synthesis of (+)-epibatidine Decarboxylative cross-coupling of mesylates catalyzed by copper/palladium systems with customized imidazolyl phosphine ligands Regioselectivity in the Stille Coupling Reactions of 3,5-Dibromo-2-pyrone The Stille Reaction Flow Chemistry Syntheses of Styrenes, Unsymmetrical Stilbenes and Branched Aldehydes New ternary ligands consisting of an N4 bridging ligand and two terpyridines, and their Co(II) and Ni(II) dinuclear complexes. Structure, redox properties, and reaction with acid Thieno[3,4-b]pyrazine-based oligothiophenes: simple models of donor-acceptor polymeric materials. A one-pot sequence of Stille and Heck couplings: synthesis of various 1,3,5-hexatrienes and their subsequent 6pi-electrocyclizations A regioselective double Stille coupling reaction of bicyclic stannolanes. Bis(benzonitrile)dichloropalladium(II)
is cites work of	wds:Q37484247-52B233B2-F5F0-46E8-9025-ECFB7D960781 wds:Q39289823-D8002D77-593A-4A62-8CB8-2CBB0991A1C4 wds:Q44602116-4A350443-7C81-4A37-A003-579698895631 wds:Q44760658-5D97D50F-BAF6-43AA-80B4-C5364891A94A wds:Q51821458-614DE5E9-0A96-43B4-B2AB-823978EBEFD5 wds:Q58118620-3B9C4EED-EB4F-4B7E-998A-D92D407BD597 wds:Q60690729-F5BA9220-6246-4D82-9AA1-F200FDB7F9E8 wds:Q38234765-154B972F-4A00-4C8D-86E8-0E4C5C728077 wds:Q56951702-D817B06F-49A3-4414-A51F-212D20A50F7B wds:Q41903560-EA77A018-D656-43D1-AAC3-9D7B89865E56 wds:Q44660296-FD6E88C6-9B85-42BA-BACC-B96786ED20D8 wds:Q48117213-058C3CFB-0E86-400B-BCDE-696C7A8422CF wds:Q46877729-5C767529-3F17-4F14-AABF-74110CB9ED5C wds:Q53076223-4D8CEFCC-D8B0-43CB-AF16-58DFCAA8915B wds:Q55885744-73D3C1B1-A51F-4BFB-8129-8A3459AEC318 wds:Q45212310-4345D610-EEED-44B4-A013-4E01B8926819 wds:Q42544411-F230B098-7280-4E05-B08C-8BCBA70C5A04 wds:Q43049371-DAFB463C-544C-4DB2-B40D-845FE3C6A30E wds:Q46873588-CFA2E15F-2EF3-4E07-829E-CC90445A4247 wds:Q43763741-BFE1FE02-9603-46BA-BAF2-721FE5739A4E wds:Q46383898-E6B7D6C3-DE83-46ED-A634-14EFF2D8AD2D wds:Q40343926-94BE6778-77E8-4FAF-9BD2-A45A1758E791 wds:Q77880124-D01E7EF3-F139-4394-A624-0E85EEC81499 wds:Q34264193-EE21DE8A-6234-4767-8BF2-C3203533F428 wds:Q43911092-EA97D78D-F569-4536-B87A-A96603728D5C wds:Q37977860-AF6879E4-A3B0-474F-A91F-C4EA383CF6D6

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