2017
DOI: 10.1007/s11164-017-3221-z
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Synthesis of 2-(ethynyloxy)naphthaene-1-carbaldehyde using 2-hydroxy benzyl alcohol and propargyl bromide in aqueous micellar media

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Cited by 8 publications
(2 citation statements)
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“…The primary method for creating 1,2,3-triazoles is the azide–alkyne cyclo-addition reaction. 24,25 As a result, the alkylation reaction of the starting materials 1a and 1b using propargyl bromide, 26 2 produced the derivatives 3a and 3b of O -alkynyl oxadiazole. Moreover, compounds 3a and 3b were used as starting materials to create a library of target compounds as quinoxaline triazole hybrids using the click reaction with ethyl 4-azidobenzoate, Cu(OAc) 2 , and ascorbate 27 ( Scheme 1 ).…”
Section: Resultsmentioning
confidence: 99%
“…The primary method for creating 1,2,3-triazoles is the azide–alkyne cyclo-addition reaction. 24,25 As a result, the alkylation reaction of the starting materials 1a and 1b using propargyl bromide, 26 2 produced the derivatives 3a and 3b of O -alkynyl oxadiazole. Moreover, compounds 3a and 3b were used as starting materials to create a library of target compounds as quinoxaline triazole hybrids using the click reaction with ethyl 4-azidobenzoate, Cu(OAc) 2 , and ascorbate 27 ( Scheme 1 ).…”
Section: Resultsmentioning
confidence: 99%
“…The analysis of surfactant aggregation along with its potential application is a hot topic in association with the studies on the effect of organized assemblies during a number of chemical transformation [21][22][23]. The applicability of a particular surfactant in a reaction is mainly determined by the nature of forming aggregates [24].…”
Section: Introductionmentioning
confidence: 99%