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Microwave-assisted synthesis of substituted fluorophenyl mono- and diazides by SNAr. A fast methodology to prepare photoaffinity labeling and crosslinking reagents
related by: authorship_20971
type: Continuant
volume: 156
type: Thing
type: Generically Dependent Continuant
origen: scopus
related by: authorship_20969
doi: 10.1016/j.jfluchem.2013.10.002
has funding vehicle: University of California, Los Angeles, UCLA
freetext keyword: Diazides; Fluoroarylazide; Microwave; Photoaffinity labeling
type: Entity
type: Information Content Entity
type: Document
page end: 169
related by: authorship_20967
has publication venue: Journal of Fluorine Chemistry
related by: authorship_20968
page start: 164
e iscopus: 2-s2.0-84886451618
most specific type: Article
estado: published
date time value: article date 3639
type: Article
abstract: The reaction of sodium azide with perfluorobenzene, containing an electron-withdrawing group, under microwave irradiation results in the fast preparation of p-substituted tetrafluorophenyl monoazides. Having an excess of sodium azide and a strong electron-withdrawing group like NO2 or CN, fluorophenyl diazides are also produced upon conventional or microwave heating. A synergic effect between the amount of sodium azide and the electron-withdrawing character of the substituents is observed giving different products. A discussion on the products and reaction mechanism is presented. © 2013 Published by Elsevier B.V.
most specific type: Document
related by: authorship_20970
crisid: 3639
has funding vehicle: Consejo Nacional de Ciencia y Tecnología, CONACYT: 290618, CB-2010-155678

Journal of Fluorine Chemistry
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type: Document
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publication venue for: Microwave-assisted synthesis of substituted fluorophenyl mono- and diazides by SNAr. A fast methodology to prepare photoaffinity labeling and crosslinking reagents
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type: Thing
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Generically Dependent Continuant
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individual
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date: 2026-08-27T13:00:28
publisher: vivo
type: Document
label: RDF description of Microwave-assisted synthesis of substituted fluorophenyl mono- and diazides by SNAr. A fast methodology to prepare photoaffinity labeling and crosslinking reagents - http://orbis.uaslp.mx/vivo/individual/scopus3638

University of California, Los Angeles, UCLA
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funding vehicle for: Microwave-assisted synthesis of substituted fluorophenyl mono- and diazides by SNAr. A fast methodology to prepare photoaffinity labeling and crosslinking reagents

Article
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Consejo Nacional de Ciencia y Tecnología, CONACYT: 290618, CB-2010-155678
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type: BFO_0000020
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type: Grant
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funding vehicle for: Microwave-assisted synthesis of substituted fluorophenyl mono- and diazides by SNAr. A fast methodology to prepare photoaffinity labeling and crosslinking reagents

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