About: Catalytic coupling of haloolefins with anilides

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scientific article published on 01 March 2005

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 2005 (uk) artículu científicu espublizáu en marzu de 2005 (ast) scientific article published on 01 March 2005 (en)
publication date	wds:Q81556786-966A8564-8785-4DC0-BC0F-F7D8D785264E
publication date	2005-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q81556786-55E36095-BEEF-4FA4-8C1F-8CE1B064E584
language of work or name	English
cites work	wds:Q81556786-193BC611-C757-4CA8-AF6B-9F23D8A7F49F
cites work	RETRACTED: Oxidative C-arylation of free (NH)-heterocycles via direct (sp3) C-H bond functionalization
author name string	wds:Q81556786-27D96B8C-7D79-40D1-9D33-2386F4EF9324 wds:Q81556786-8ED94613-6AFF-4C74-941F-7C0972A55535
author name string	Olafs Daugulis Vladimir G Zaitsev
rdfs:label	Catalytic coupling of haloolefins with anilides (en) Catalytic coupling of haloolefins with anilides (nl)
skos:prefLabel	Catalytic coupling of haloolefins with anilides (en) Catalytic coupling of haloolefins with anilides (nl)
name	Catalytic coupling of haloolefins with anilides (en) Catalytic coupling of haloolefins with anilides (nl)
title	wds:Q81556786-954F5BD5-F940-4D60-BBE7-5D94F5D95F17
title	Catalytic coupling of haloolefins with anilides (en)
page(s)	wds:Q81556786-18A10E08-3771-4B86-B8D4-AB6E5D304D14
page(s)	4156-4157
instance of	wds:Q81556786-69A4A067-EEA4-4FA3-ABC8-CEE0B07F76E5
instance of	scholarly article
PubMed ID	wds:Q81556786-435D04A1-F202-4879-AFA8-93AA6E6D03E6
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15783182
PubMed ID	15783182
published in	wds:Q81556786-8E71CE16-0EFA-45BE-BF67-9B559F0055EB
published in	Journal of the American Chemical Society
issue	wds:Q81556786-74755AFB-3FC4-40C4-BA48-D9877F134E99
volume	wds:Q81556786-28416270-255A-479A-84D4-73CAA557069E
issue	12
volume	127
DOI	wds:Q81556786-F921B4F6-AE87-42CE-BE39-A0C34D7C05C4
DOI	http://dx.doi.org/10.1021/JA050366H
DOI	10.1021/JA050366H
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q81556786
is cites work of	Constructing multiply substituted arenes using sequential palladium(II)-catalyzed C-H olefination N-acylsulfonamide assisted tandem C-H olefination/annulation: synthesis of isoindolinones Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality Pd(II)-catalyzed hydroxyl-directed C-H olefination enabled by monoprotected amino acid ligands Ligand-accelerated C-H activation reactions: evidence for a switch of mechanism Direct transition metal-catalyzed functionalization of heteroaromatic compounds Insights into directing group ability in palladium-catalyzed C-H bond functionalization Synthetic and mechanistic studies of Pd-catalyzed C-H arylation with diaryliodonium salts: evidence for a bimetallic high oxidation state Pd intermediate Pd(II)-catalyzed olefination of sp3 C-H bonds Amide-Directed Arylation of sp C-H Bonds using Pd(II) and Pd(0) Catalysts Pd(II)-catalyzed olefination of electron-deficient arenes using 2,6-dialkylpyridine ligands Bystanding F+ oxidants enable selective reductive elimination from high-valent metal centers in catalysis An Improved Catalyst Architecture for Rhodium (III) Catalyzed C-H Activation and its Application to Pyridone Synthesis Enantioselective Fujiwara-Moritani Indole and Pyrrole Annulations Catalyzed by Chiral Palladium(II)-NicOx Complexes All-Carbon-Substituted Quaternary Carbon Atoms in Oxindoles by an Aerobic Palladium(II)-Catalyzed Ring Closure onto Tri- and Tetrasubstituted Double Bonds Direct palladium-catalyzed alkynylation of N-fused heterocycles Exclusive 5-exo-dig hydroarylation of o-alkynyl biaryls proceeding via C-H activation pathway Remote, Late-Stage Oxidation of Aliphatic C-H Bonds in Amide-Containing Molecules. Synthesis of phenanthridines via palladium-catalyzed picolinamide-directed sequential C-H functionalization. Palladium-Catalyzed Synthesis of Aromatic Sultones via Sulfonic Acid Group-Directed CH Activation Palladium-Catalysed Synthesis of α-(Trifluoromethyl)styrenes by Means of Directed C-H Bond Functionalization Palladium-catalyzed acid-free Fujiwara-Moritani alkenylation of 4-thiazolidinones. Palladium(II)-Catalyzed Regioselective Ortho Arylation of sp(2) C-H Bonds of N-Aryl-2-amino Pyridine Derivatives
is cites work of	wds:Q42544426-A640AAFC-63B1-41F5-8123-FBD1E6047D65 wds:Q57614613-2D35393A-7FB5-4A80-A74B-0774250E2697 wds:Q29012891-BEEE05E4-2355-4DC6-9FF9-8205D00225EA wds:Q43095444-15E477E8-B344-4BB1-B7F9-568C58379FC8 wds:Q36941982-18AD64C9-15C5-49F8-A3B1-6C9BAE35B395 wds:Q42636203-8DD5C7C7-104F-43C7-9B5A-0949E47400B6 wds:Q42537260-CFE18380-441F-44EC-8C57-9A085F239C2B wds:Q59203473-B1867506-20A4-477D-B0C7-10B8C3B4AC84 wds:Q37294999-ACCD38CF-9AFE-45B2-B341-8B04D992DE6E wds:Q33899813-82BCA3A0-57B4-4836-8D90-AD02C0A665CE wds:Q34061734-2A3A2BE9-E01A-4674-BC1B-CB19FD181CD1 wds:Q40773580-5B1AFE89-4167-475B-87AD-5A0BADF20A25 wds:Q59203498-FEEDACC8-2923-4ED0-985D-B2B02E17E98B wds:Q33738148-7F122552-177C-49B6-B2E5-9CF22985A4A1 wds:Q37154137-B0B698C6-0A5E-4A78-A6C8-F8B9479E02E6 wds:Q48330898-09545CB3-909A-4676-9C1C-E9D59745B572 wds:Q53217066-189F53D1-8981-475D-8C2A-73A58F68AB47 wds:Q59071306-D1742450-0466-4EE0-93FB-FBB8B91110EF wds:Q36852312-23097D4C-2698-465D-9C0B-352FA955739A wds:Q41647791-492FF6DF-CEEC-4C35-8AE9-A86F4C4EB3D7 wds:Q42095811-7E42EB46-1ACD-41E8-8270-3DCE9428465A wds:Q42161197-9C8CF7D9-3CE6-46B6-BDF0-DC7F5EFABC8F wds:Q37832211-8480684D-6420-4782-92D8-083C2C70ECC0 wds:Q36908149-75FF8D23-4A6A-4731-86E6-DC477C8F78F7

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