About: 1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols

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About: 1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols Goto Sponge NotDistinct Permalink

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scientific article published on 01 November 2006

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rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2006 (fr) наукова стаття, опублікована в листопаді 2006 (uk) im November 2006 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en payares de 2006 (ast) scientific article published on 01 November 2006 (en)
publication date	wds:Q62580155-BBE86A96-ECF3-4851-A9DC-8384648BE8F4
publication date	2006-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q62580155-00DC47A7-3E09-4C6D-B7F5-D16FF46366D8
language of work or name	English
author name string	wds:Q62580155-18DBFAF3-18D8-414C-8E77-8F5815E4C9D7 wds:Q62580155-F2BFB51D-59B6-49D2-8EEC-8B82810A56C7
author name string	Hsin-Hung Chen Yao-Jung Chen
rdfs:label	1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols (en) 1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols (nl)
skos:prefLabel	1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols (en) 1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols (nl)
name	1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols (en) 1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols (nl)
title	wds:Q62580155-749BF803-47F9-4FA2-8994-16019C5BB14C
title	1,1,1-tris(hydroxymethyl)ethane as a new, efficient, and versatile tripod ligand for copper-catalyzed cross-coupling reactions of aryl iodides with amides, thiols, and phenols (en)
page(s)	wds:Q62580155-C5636D42-C5ED-49CE-9F28-DCDC823FCADB
page(s)	5609-5612
instance of	wds:Q62580155-39DADFB7-A2B0-4781-B610-6C8EEF4469A4
instance of	scholarly article
PubMed ID	wds:Q62580155-ADD3E334-A384-40FC-BCC4-D520B81ACDFC
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17107084
PubMed ID	17107084
published in	wds:Q62580155-27C19302-F95D-4264-AF7F-93C431976E9F
published in	Organic Letters
issue	wds:Q62580155-52DC53AC-A629-4780-8CCC-DAF4BB940059
volume	wds:Q62580155-27CF06F6-830C-44CC-911C-68FC5DEAC9FC
issue	24
volume	8
DOI	wds:Q62580155-14A388AF-FF8F-40E1-8778-6ACDCDE77579
DOI	http://dx.doi.org/10.1021/OL062339H
DOI	10.1021/OL062339H
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q62580155
is cites work of	Computational explorations of mechanisms and ligand-directed selectivities of copper-catalyzed Ullmann-type reactions Copper complexes of anionic nitrogen ligands in the amidation and imidation of aryl halides Cu-catalyzed arylation of phenols: synthesis of sterically hindered and heteroaryl diaryl ethers Diamine Ligands in Copper-Catalyzed Reactions Transition metal catalyzed synthesis of aryl sulfides. Highly efficient and reusable copper-catalyzed N-arylation of nitrogen-containing heterocycles with aryl halides. Resting state and elementary steps of the coupling of aryl halides with thiols catalyzed by alkylbisphosphine complexes of palladium First application of an efficient and versatile ligand for copper-catalyzed cross-coupling reactions of vinyl halides with N-heterocycles and phenols Copper(I) phenoxide complexes in the etherification of aryl halides Synthesis of Copper(I) Thiolate Complexes in the Thioetherification of Aryl Halides Base-mediated stereospecific synthesis of aryloxy and amino substituted ethyl acrylates. An efficient heterogeneous catalyst (CuO@ARF) for on-water C-S coupling reaction: an application to the synthesis of phenothiazine structural scaffold Copper/N,N-dimethylglycine catalyzed goldberg reactions between aryl bromides and amides, aryl iodides and secondary acyclic amides. Copper Mediated Coupling of 2-(Piperazine)-pyrimidine Iodides with Aryl Thiols using Cu(I)Thiophene-2-carboxylate Copper-catalyzed N-arylation of amides using (S)-N-methylpyrrolidine-2-carboxylate as the ligand. Nanoflowers of Cu<sub>1.8</sub>S: Free and Decorated on Graphene Oxide (GO–Cu<sub>1.8</sub>S) as Efficient and Recyclable Catalysts for C–O Coupling Nano copper oxide catalyzed synthesis of symmetrical diaryl sulfides under ligand free conditions RECENT SYNTHETIC DEVELOPMENTS AND APPLICATIONS OF THE ULLMANN REACTION. A REVIEW Metal-Free Synthesis of Secondary Arylamines: An Aliphatic-to-Aromatic Transformation Synthesis of a Regioregular Series of Poly(aryl ether carbonates) and Their Glass Transition Temperatures
is cites work of	wds:Q42148622-E5325FAD-75E8-4BA9-83B9-47E639050389 wds:Q53485666-ACFB1DD5-30F0-43C8-AA5B-35D99BF83E7D wds:Q59320736-A87995BD-A8A9-4A49-A9B2-E6D85547A560 wds:Q53459137-89A3878D-E8C5-4E35-912C-B106A581E7C8 wds:Q90351559-BBE1BF14-95AA-46C4-B4CC-B5A1D20E6B06 wds:Q36519046-C0D0A9FD-30F9-4C4D-8E60-1AB108D03D01 wds:Q37829632-72544270-6BBE-452D-BAEE-5D1B39D175EF wds:Q42141792-67495182-3E57-406C-89FD-67552BB7CE12 wds:Q43119472-184E30C4-80E0-4AB0-AB07-18A96AEFDFDD wds:Q40250916-56BF81CD-4C26-4DA3-80B8-8BCA19AF327A wds:Q114258815-924AAF90-F8B5-4E48-A673-8E1032FE8515 wds:Q60690645-EBC78E9A-6C45-442E-81F7-EB8105DBC495 wds:Q92466049-0F23EFC7-EE66-49DE-9A12-B4564F6CD20E wds:Q34432880-F3706939-BCF4-4BE6-AB2A-7F450C872CD8 wds:Q35786838-5052CD0F-6871-4DFE-9342-F4614AB981E0 wds:Q34013661-49F9951E-3038-4889-94D9-944381C1C311 wds:Q35040494-0DA085BF-2134-41B4-9666-E997C128D841 wds:Q35124625-127F05C5-206D-4714-92B1-DBB685EBBE4F wds:Q40001481-A58152FE-FB8D-4D64-B7EA-044CA7F3570A wds:Q42027004-D2199551-8843-4CA0-B81F-1BBDAA07EDE3

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