About: Room-Temperature Decarboxylative Alkynylation of Carboxylic Acids Using Photoredox Catalysis and EBX Reagents

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scientific article published on 24 July 2015

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в липні 2015 (uk) im Juli 2015 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 24 July 2015 (en) artículu científicu espublizáu en xunetu de 2015 (ast)
publication date	wds:Q64169033-67CE125D-5259-4C17-808A-6B9D51AE7B31
publication date	2015-07-24 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q64169033-38EE7FC2-840C-4121-A3E7-4F3E5FA0DB38
language of work or name	English
author name string	wds:Q64169033-2E233105-7487-4616-863E-3D09C53F9E7C wds:Q64169033-8BBAF258-5625-45F4-A6DD-AD2C4FCBEF8B
author name string	Franck Le Vaillant Thibaut Courant
rdfs:label	Room-Temperature Decarboxylative Alkynylation of Carboxylic Acids Using Photoredox Catalysis and EBX Reagents (en) Room-Temperature Decarboxylative Alkynylation of Carboxylic Acids Using Photoredox Catalysis and EBX Reagents (nl)
skos:prefLabel	Room-Temperature Decarboxylative Alkynylation of Carboxylic Acids Using Photoredox Catalysis and EBX Reagents (en) Room-Temperature Decarboxylative Alkynylation of Carboxylic Acids Using Photoredox Catalysis and EBX Reagents (nl)
name	Room-Temperature Decarboxylative Alkynylation of Carboxylic Acids Using Photoredox Catalysis and EBX Reagents (en) Room-Temperature Decarboxylative Alkynylation of Carboxylic Acids Using Photoredox Catalysis and EBX Reagents (nl)
author	wds:Q64169033-4ABB74BB-EA5C-4023-B916-02AC93C52057
author	Jerome Waser
title	wds:Q64169033-B5DB1CA7-6B94-47AC-99B0-9209F53BF656
title	Room-temperature decarboxylative alkynylation of carboxylic acids using photoredox catalysis and EBX reagents (en)
page(s)	wds:Q64169033-25F621B2-5840-4351-AC50-A8843931D881
page(s)	11200-11204
instance of	wds:Q64169033-DE8B623E-4602-4472-AB4E-0573B89330A4
instance of	scholarly article
PubMed ID	wds:Q64169033-E94D7D57-7226-4967-94EF-29651FA8CA13
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26212356
PubMed ID	26212356
published in	wds:Q64169033-0F8447F5-ECFB-4F8E-B897-4E8D4C14A744
published in	Angewandte Chemie International Edition
issue	wds:Q64169033-0AF34848-C6B6-4EB8-A1B0-8392F0B63EE8
volume	wds:Q64169033-8A7CFAB6-7CBE-4F71-8E34-43217F28E597
issue	38
volume	54
DOI	wds:Q64169033-892FEF52-14EB-4A93-A34A-57AECAD09D5B
DOI	http://dx.doi.org/10.1002/ANIE.201505111
DOI	10.1002/ANIE.201505111
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q64169033
is cites work of	Photoredox Catalysis in Organic Chemistry Photoredox-mediated Minisci C-H alkylation of N-heteroarenes using boronic acids and hypervalent iodine Room temperature decarboxylative cyanation of carboxylic acids using photoredox catalysis and cyanobenziodoxolones: a divergent mechanism compared to alkynylation Photoredox Imino Functionalizations of Olefins. Decarboxylative Alkynylation. Iodine(III) Reagents in Radical Chemistry Palladium-Catalyzed Enantioselective Redox-Relay Heck Alkynylation of Alkenols To Access Propargylic Stereocenters. Reductive Decarboxylative Alkynylation of N-Hydroxyphthalimide Esters with Bromoalkynes. Photoinduced Remote Functionalization of Amides and Amines Using Electrophilic Nitrogen Radicals Fine-tuned organic photoredox catalysts for fragmentation-alkynylation cascades of cyclic oxime ethers Investigations of alkynylbenziodoxole derivatives for radical alkynylations in photoredox catalysis. Light-Driven Intermolecular Charge Transfer Induced Reactivity of Ethynylbenziodoxol(on)e and Phenols Photoredox-mediated remote C(sp3)-H heteroarylation of free alcohols
is cites work of	wds:Q42291057-D302D637-3D61-439D-8FBF-41981EDB1C40 wds:Q28829372-9E3596EB-BCE1-48B9-B2E0-74FA5C8CE0D2 wds:Q55431211-A64574A4-6199-4828-901F-1C5612C88A77 wds:Q41136755-2A3EAE05-40BE-4335-9FC1-3B3D05ECC5BC wds:Q91667064-0AF9F8CB-87FD-450B-BC91-BA81DDE4DB50 wds:Q48245463-768EC569-C2F9-4073-A12F-94294C934CB5 wds:Q57046872-F6A91C41-2386-4AE6-A441-2940478BFFCB wds:Q41137826-379A80E1-1F5E-48B2-8C92-98118401DD61 wds:Q41938825-284637AA-7026-49CA-86F0-17D663F19E03 wds:Q47128255-EBB27BE8-6668-481A-A06C-E40B2C12B0CC wds:Q48282145-06C8086F-F652-46A9-8127-664AF5372C08 wds:Q61926931-04905F6A-4784-4604-A2BE-099BFC9D6C52 wds:Q60494093-E21D44E4-E861-4457-9A01-03A710C82006

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