About: Synthesis, structure, and reductive elimination chemistry of three-coordinate arylpalladium amido complexes

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scientific article published on 01 May 2004

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 2004 (uk) artículu científicu espublizáu en mayu de 2004 (ast) scientific article published on 01 May 2004 (en)
publication date	wds:Q80005402-113413F0-88D2-4ADE-96AB-A7CDBF03DFEB
publication date	2004-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q80005402-7B6AFF9F-5CD7-4052-8D9C-61A17B674BE6
language of work or name	English
cites work	wds:Q80005402-651DCEF7-7AE6-4440-82F1-1A2EEA701292
cites work	Mechanism of thermal decomposition of trans-diethylbis(tertiary phosphine)palladium(II). Steric effects of tertiary phosphine ligands on the stability of diethylpalladium complexes
author name string	wds:Q80005402-B083F994-C23A-41D0-AB1A-350AA5F0C855
author name string	John F Hartwig
rdfs:label	Synthesis, structure, and reductive elimination chemistry of three-coordinate arylpalladium amido complexes (en) Synthesis, structure, and reductive elimination chemistry of three-coordinate arylpalladium amido complexes (nl)
skos:prefLabel	Synthesis, structure, and reductive elimination chemistry of three-coordinate arylpalladium amido complexes (en) Synthesis, structure, and reductive elimination chemistry of three-coordinate arylpalladium amido complexes (nl)
name	Synthesis, structure, and reductive elimination chemistry of three-coordinate arylpalladium amido complexes (en) Synthesis, structure, and reductive elimination chemistry of three-coordinate arylpalladium amido complexes (nl)
author	wds:Q80005402-009B2647-0686-4835-A834-5ECF0365792E
author	Makoto Yamashita
title	wds:Q80005402-EA81D509-0636-4C85-B498-93E8081576F3
title	Synthesis, structure, and reductive elimination chemistry of three-coordinate arylpalladium amido complexes (en)
page(s)	wds:Q80005402-78E1D136-038A-4C8C-BE24-8BAC800D3576
page(s)	5344-5345
instance of	wds:Q80005402-50E5454D-E096-4C65-8F80-43E3EBB83617
instance of	scholarly article
PubMed ID	wds:Q80005402-53B59EDD-63FF-4D1F-AC89-D5AEC953C3A2
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15113190
PubMed ID	15113190
published in	wds:Q80005402-ED846989-D541-4000-9468-979A2C7688BB
published in	Journal of the American Chemical Society
issue	wds:Q80005402-76243C87-3D84-443D-8636-6526534BEA80
volume	wds:Q80005402-44177052-A487-4B83-9752-1DA37AA40921
issue	17
volume	126
DOI	wds:Q80005402-338A5BD0-F7AE-438F-84BD-27D2F9332312
DOI	http://dx.doi.org/10.1021/JA0315107
DOI	10.1021/JA0315107
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q80005402
is cites work of	Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides Lewis acid acceleration of C-N bond-forming reductive elimination from heteroarylpalladium complexes and catalytic amidation of heteroaryl bromides Probing the Electronic Demands of Transmetalation in the Palladium-Catalyzed Cross-Coupling of Arylsilanolates Stable cyclic carbenes and related species beyond diaminocarbenes Rational ligand design for the arylation of hindered primary amines guided by reaction progress kinetic analysis New strategy for the synthesis of substituted morpholines A rigid cyclic (alkyl)(amino)carbene ligand leads to isolation of low-coordinate transition-metal complexes Reductive elimination of ether from T-shaped, monomeric arylpalladium alkoxides Nickel-catalyzed amination of aryl carbamates and sequential site-selective cross-couplings. Palladium-catalyzed alkene carboamination reactions for the synthesis of substituted piperazines Assessment of the intermediacy of arylpalladium carboxylate complexes in the direct arylation of benzene: evidence for C-H bond cleavage by "ligandless" species Biaryl Phosphine Based Pd(II) Amido Complexes: The Effect of Ligand Structure on Reductive Elimination True and masked three-coordinate T-shaped platinum(II) intermediates Oxygen Activated, Palladium Nanoparticle Catalyzed, Ultrafast Cross-Coupling of Organolithium Reagents Olefin-accelerated solid-state C-N cross-coupling reactions using mechanochemistry Mechanochemistry allows carrying out sensitive organometallic reactions in air: glove-box-and-Schlenk-line-free synthesis of oxidative addition complexes from aryl halides and palladium(0) Oxygen Activated, Palladium Nanoparticle Catalyzed, Ultrafast Cross-Coupling of Organolithium Reagents. Palladium-Catalyzed C-O Cross-Coupling of Primary Alcohols.
is cites work of	wds:Q35076603-3E2D2416-42B2-4748-80E5-853635D27EC3 wds:Q64028386-E64C57F4-1819-4703-B2FB-E2F09870C081 wds:Q60912734-054B7862-6F73-4100-9CF9-A75B922A9039 wds:Q42919982-9A7F9F52-3670-4ED4-86B8-FFCDBE6B08D2 wds:Q43094737-7E1D7C7B-829A-4ADB-9E1E-9E7DC0189C4B wds:Q38129059-0C435A22-BB86-4427-BA5B-B83DB3B3B2D0 wds:Q48241470-A18250A3-8218-44DC-8DB6-D2201E6788E1 wds:Q37788080-DCBC79D1-2810-4E04-8502-A5DD54E90E46 wds:Q41901146-062CA795-5BA0-42F8-846E-F665B168BF87 wds:Q91784350-2340195A-FD5A-4164-8814-90AFA2B385FE wds:Q59707125-090DBFC6-ABD9-4473-9E38-858DECC966F3 wds:Q39141061-CF2AF451-9A5C-4061-8F36-5B926EB07E12 wds:Q42140088-522163AD-A6DA-4D22-90E1-D07DF0F85880 wds:Q29302487-589D4FE2-DC8E-4B74-A0B8-07835F3BEBA9 wds:Q35233786-48CCF58C-371B-4277-9650-7B1ED8832C6B wds:Q41950081-2D027F1F-703B-4753-82ED-241E3850138F wds:Q41870553-B0921D5F-8A18-4CB4-AE9C-0134476B9FA0 wds:Q52688495-82F5AA88-4ED1-4622-BF6C-54DE5BAEA4F9

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