About: Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study

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About: Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study Goto Sponge NotDistinct Permalink

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description	wetenschappelijk artikel (nl) article scientifique publié en 2016 (fr) наукова стаття, опублікована в листопаді 2016 (uk) im November 2016 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q63413889-11F885CE-0543-4893-81A6-2F05AB0F6456
publication date	2016-11-18 00:00:00Z (xsd:dateTime)
cites work	wds:Q63413889-00A71EFB-1286-4A22-A984-C255FF4421AF wds:Q63413889-017D1220-2873-4B35-A844-D7583745917B wds:Q63413889-08C738B0-2627-4B05-9C4E-F4B2F56C3EDC wds:Q63413889-14C5CFA3-47F0-4DF1-A440-36CF7F961B80 wds:Q63413889-21260050-8BD1-45B5-AAB3-D2588860A3AA wds:Q63413889-29AC0ED2-3E69-40EE-8727-77F340DE0A7E wds:Q63413889-373C569B-19F0-4D58-9D03-7C64FBD4F788 wds:Q63413889-39AC12C2-9F81-4DC0-BE25-BDB0BF2F9A50 wds:Q63413889-492CAAA3-4378-4F00-B91F-901E4E244CC8 wds:Q63413889-4C25E776-F6C7-4ED6-9985-6FEE8D6F3E38 wds:Q63413889-56DB32F4-CBFF-4DFF-A819-861285573C31 wds:Q63413889-5708A078-64E8-49C2-978E-9D5BA4812EA6 wds:Q63413889-661C4DCC-631B-4EF7-91FC-784D7C78E104 wds:Q63413889-6A19D8C1-7C78-4DB3-92E4-726F29743983 wds:Q63413889-6AAEED22-BD8E-478E-B33F-32ECC0D2554A wds:Q63413889-6B15ADEC-AC5C-44C6-8330-7001F4F7F90C wds:Q63413889-6BAEACAD-28F4-43AC-A1BC-DE6A6BF79D09 wds:Q63413889-7270B33B-CDC5-4235-9FFF-D16533EBEF21 wds:Q63413889-7487A96A-CB78-48D3-B818-2C9DE619EB71 wds:Q63413889-7BDB138F-E2DA-45F8-A3F3-4595A9013E39 wds:Q63413889-9BB2C3A8-2028-4686-82E2-5A8AECF087D5 wds:Q63413889-9EC6AA7B-8D28-426A-AFAA-43A313B8600F wds:Q63413889-9FE8155B-C93C-4B05-ACA7-CB353634392E wds:Q63413889-B495E5DE-3EF1-41D1-AB86-A054D0A297EA wds:Q63413889-BE43AB24-2952-48F3-B79A-5E369FAD9773 wds:Q63413889-D16F6BAA-1FFD-44C4-8ED9-EF2753DA2E22 wds:Q63413889-D9C6B68A-0F82-46C0-9B69-0188709D3F99 wds:Q63413889-D9F7AA59-B26F-4798-86FD-D998C485B2E9 wds:Q63413889-DA13C27C-61B3-4396-A25F-30D765AF3144 wds:Q63413889-E88D3157-7E5F-49AA-9705-5D223963DD88 wds:Q63413889-E96A2683-A874-4E9E-880B-D37729861585 wds:Q63413889-EAE9D939-622F-4EEE-9F98-9EA7384E4671 wds:Q63413889-EE3AA414-648C-45B1-A04B-6036FC3BECA2 wds:Q63413889-EFB647B8-5C26-4065-B68E-9EB6F851F398 wds:Q63413889-F1166F3B-3A78-41D7-A2E1-A631D5EFE4EB wds:Q63413889-F2B273FA-0691-4441-9F99-C23E6C2451F3
cites work	Copper-mediated coupling reactions and their applications in natural products and designed biomolecules synthesis Catalytic CC, CN, and CO Ullmann-Type Coupling Reactions Ueber Phenylirungen bei Gegenwart von Kupfer als Katalysator Selected patented cross-coupling reaction technologies Quantum mechanical continuum solvation models. Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions Computational explorations of mechanisms and ligand-directed selectivities of copper-catalyzed Ullmann-type reactions Alternative mechanistic explanation for ligand-dependent selectivities in copper-catalyzed N- and O-arylation reactions. CuI/Oxalic Diamide Catalyzed Coupling Reaction of (Hetero)Aryl Chlorides and Amines The mechanism of the modified Ullmann reaction Triazenes: a versatile tool in organic synthesis Removal of amino groups from anilines through diazonium salt-based reactions Recent applications of arene diazonium salts in organic synthesis Silver-mediated trifluoromethylation of aryldiazonium salts: conversion of amino group into trifluoromethyl group. Sustainable Heck-Matsuda reaction with catalytic amounts of diazonium salts: an experimental and theoretical study. A highly efficient Cu-catalyzed S-transfer reaction: from amine to sulfide. The virtue of the multifunctional triazene linkers in the efficient solid-phase synthesis of heterocycle libraries Alkyl nitrite-metal halide deamination reactions. 6. Direct synthesis of arenediazonium tetrafluoroborate salts from aromatic amines, tert-butyl nitrite, and boron trifluoride etherate in anhydrous media Radical reactions of arenediazonium ions: An easy entry into the chemistry of the aryl radical Cp*Ir(III)-Catalyzed Mild and Broad C-H Arylation of Arenes and Alkenes with Aryldiazonium Salts Leading to the External Oxidant-Free Approach. The First Stable Diazonium Ion on Solid Support-Investigations on Stability and Usage as Linker and Scavenger in Solid-Phase Organic Synthesis Nitrogen-Based Linkers, Part 8. This work was supported by the Fonds der Chemischen Industrie (Liebig-Stip A family of low molecular-weight, organic catalysts for reductive C-C bond formation Ligand-Assisted Gold-Catalyzed Cross-Coupling with Aryldiazonium Salts: Redox Gold Catalysis without an External Oxidant. Ueber die Ersetzung der Amidgruppe durch Chlor in den aromatischen Substanzen Sandmeyer trifluoromethylation of arenediazonium tetrafluoroborates. Heck-Matsuda Arylation of Olefins Through a Bicatalytic Approach: Improved Procedures and Rationalization CuI/Oxalamide Catalyzed Couplings of (Hetero)aryl Chlorides and Phenols for Diaryl Ether Formation Convenient and General Palladium-Catalyzed Carbonylative Sonogashira Coupling of Aryl Amines Vorläufige Notiz über die Einwirkung von salpetriger Säure auf Amidinitro- und Aminitrophenylsäure Copper-promoted sandmeyer difluoromethylthiolation of aryl and heteroaryl diazonium salts Copper(I) Acetate Copper-catalyzed arylation of nitrogen heterocycles from anilines under ligand-free conditions Catalytic Sandmeyer Bromination THEORETICAL STUDY ON CUI-CATALYZED LIGAND-FREE N-ARYLATION OF IMIDAZOLE WITH BROMOBENZENE Detection of Aryl Radicals in Hydrodediazoniations Copper- or iron-catalyzed arylation of phenols from respectively aryl chlorides and aryl iodides
author name string	wds:Q63413889-0C78409A-D328-4A1C-A2CB-B12CFF94470D wds:Q63413889-285C0E16-8024-4D9B-B4BB-4CBF01973020 wds:Q63413889-333BA652-69F3-4A35-ABA9-932012787015 wds:Q63413889-4140A1A6-3F3F-467B-AE57-0BA8274B7095 wds:Q63413889-7DC5A4F1-9A42-40C0-B552-C36C29646998 wds:Q63413889-CA910AE9-1EE1-4E1E-AFF5-E4D8A1E395C6
author name string	Ilaria Ciofini Marc Taillefer Laurence Grimaud Indira Fabre Julien Bergès Luca Alessandro Perego
rdfs:label	Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study (en) Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study (nl)
skos:prefLabel	Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study (en) Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study (nl)
name	Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study (en) Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study (nl)
title	wds:Q63413889-7EF75DB1-F60E-4FB6-BF4E-6C2DAD8BC150
title	Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study (en)
page(s)	wds:Q63413889-46F4CB29-B271-421D-8743-120C0069D570

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