About: Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3)

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About: Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3) Goto Sponge NotDistinct Permalink

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article by Arturo L. Casado & Pablo Espinet published September 1998 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 1998 (uk) im September 1998 veröffentlichter wissenschaftlicher Artikel (de) article by Arturo L. Casado & Pablo Espinet published September 1998 in Journal of the American Chemical Society (en)
publication date	wds:Q56700089-BA8AF9FB-A1F1-475D-8AF0-187FFA555BA6
publication date	1998-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56700089-90FCD208-EE9A-4FA8-9C86-5ED470CDB134
language of work or name	English
author name string	wds:Q56700089-05A8A7E6-F105-499F-9FB9-D7204F4D4EB0
author name string	Arturo L. Casado
rdfs:label	Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3) (en) Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3) (nl)
skos:prefLabel	Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3) (en) Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3) (nl)
name	Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3) (en) Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3) (nl)
author	wds:Q56700089-4B51680E-1403-4A7C-9496-6B2970D6CF94
author	Pablo Espinet
title	wds:Q56700089-2E8584CC-AC50-49AF-80A4-DB88CF452F79
title	Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3) (en)
page(s)	wds:Q56700089-EDFD9832-D8ED-48CD-8383-C6141675839D
page(s)	8978-8985
instance of	wds:Q56700089-3467E414-D8F6-480A-85E5-5CDEB934D3C1
instance of	scholarly article
published in	wds:Q56700089-7CA8133D-22F9-4D61-9137-B16A1D6F43A1
published in	Journal of the American Chemical Society
issue	wds:Q56700089-599D4F23-754A-4F64-8E51-EF1BA4391237
volume	wds:Q56700089-217E7620-F9D4-4E5F-BBD0-BEE6D876A4A6
issue	35
volume	120
DOI	wds:Q56700089-2B9F547F-EDAF-49FD-9FD6-42534E10BFA2
DOI	http://dx.doi.org/10.1021/JA9742388
DOI	10.1021/JA9742388
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56700089
is cites work of	Theoretical aspects of palladium-catalysed carbon-carbon cross-coupling reactions The mechanism of the oxidative addition of aryl halides to Pd-catalysts: a DFT investigation Palladium Round Trip in the Negishi Coupling of trans-[PdMeCl(PMePh2)2] with ZnMeCl: An Experimental and DFT Study of the Transmetalation Step Stille coupling involving bulky groups feasible with gold cocatalyst The decisive role of ligand metathesis in Au/Pd bimetallic catalysis. Catalytic cross-coupling reactions mediated by palladium/nucleophilic carbene systems A theoretical DFT-based and experimental study of the transmetalation step in Au/Pd-mediated cross-coupling reactions. Dimeric palladium complexes with bridging aryl groups: when are they stable? Rate and mechanism of the oxidative addition of phenyl iodide to Pd0 ligated by triphenylarsine: evidence for the formation of a T-shaped complex Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to IV. 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 Stable Nickel Catalysts for Fast Norbornene Polymerization: Tuning Reactivity Mechanism of copper-free Sonogashira reaction operates through palladium-palladium transmetallation Mechanistic studies on the SCS-pincer palladium(II)-catalyzed tandem stannylation/electrophilic allylic substitution of allyl chlorides with hexamethylditin and benzaldehydes Structural and dynamic studies in solution of anionic dinuclear azolato-bridged palladium(II) complexes Polymer [Pd(CH2SO2C6H4Me)2]n, a precursor to remarkably stable Pd organometallics.
is cites work of	wds:Q46956225-7409688B-9276-41A1-80E0-E036FE029E0B wds:Q43644613-EDEAEB52-C35B-4277-995E-82460E2A0C4A wds:Q29307870-05F84040-1B70-46ED-91A5-7B725C569BF2 wds:Q57398029-7543DC1D-A96C-452E-AA06-155DAC88E156 wds:Q60165773-E9484E49-D3EA-4DAE-A8AE-31AA62E5AF00 wds:Q44660296-A65B9AC6-D484-44D8-B85D-F5AA93F1B6AF wds:Q38206709-C82A176C-6D5A-44E9-96BD-B40F8576CC99 wds:Q45212310-37D66CCD-F7AF-4549-B66D-62DB43597709 wds:Q44114805-E085FDF2-D838-4EAC-B925-F0ABA93046AB wds:Q46873588-1F6F0992-9441-40F8-B56E-3BE0DB987928 wds:Q37737101-308DEAD8-DBC0-40AF-A766-5A560E304A95 wds:Q60165787-2B47F3C9-EC13-47D0-A63E-B94061EED2FF wds:Q36399252-F1A0BFE0-FE14-4070-BA90-001BD23E6FB2 wds:Q54783679-B7D6A630-7937-41F4-825D-A1B4E2697BAF wds:Q60491610-495BC177-44A4-4B4B-9966-C616A8F27B1A wds:Q45154196-8E34FB86-9DFB-452F-BE80-F20C41ACD99C wds:Q59136626-012196C2-CB4F-42F5-AD63-EB6B5E5C259E

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