2016
DOI: 10.1016/j.jcat.2016.09.022
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Copper-γ-cyclodextrin complexes immobilized on hexagonal boron nitride as an efficient catalyst in the multicomponent synthesis of 1,2,3-triazoles

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Cited by 20 publications
(10 citation statements)
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“…12b) [114], refluxing in concentrated strong acids or bases [115,116], solution-phase oxygen radical reaction [117], using urea with a ball milling process, using molten hydroxides [118], or direct hydrothermal reaction with hydrogen peroxide. The hydroxylated h-BN sheets can be diversely derivatized using a silylation reaction with various silane compounds [119,120]. Despite those efforts, the membrane applications of h-BN sheets were restricted owing to their low exfoliation and production yield.…”
Section: Surface Functionalization Of H-bnmentioning
confidence: 99%
“…12b) [114], refluxing in concentrated strong acids or bases [115,116], solution-phase oxygen radical reaction [117], using urea with a ball milling process, using molten hydroxides [118], or direct hydrothermal reaction with hydrogen peroxide. The hydroxylated h-BN sheets can be diversely derivatized using a silylation reaction with various silane compounds [119,120]. Despite those efforts, the membrane applications of h-BN sheets were restricted owing to their low exfoliation and production yield.…”
Section: Surface Functionalization Of H-bnmentioning
confidence: 99%
“…h-BN nanosheets used with βCD and Pd(OAc) 2 found to be efficient in Heck couplings (see Scheme 22) [134] were also shown to be equally effective in triazole synthesis in combination with γCD and Cu(OAc) 2 [catalyst 1.7 % Cu(OAc) 2 :61-γCD-h-BN]. [174] The presence of Cu 2 + ions was shown by XPS binding energies of 934.1 eV (Cu 2p 3/2 ) and 954.0 eV (Cu 2p 1/2 ). In this case, alkynes were reacted with arylboronic acids in a two-step protocol in one pot.…”
Section: Multicomponent Reactionsmentioning
confidence: 99%
“…However, recent publications have described the use of Cu(II) complexes as catalysts without the use of reducing agents. [113][114][115][116][117][118][119][120] Bagherzadeh et al 121 reported in 2019 the preparation of two Cu(II) complexes (Figure 6) and studied their catalytic potentials against the CuAAC reaction in the absence of reducing agents. The authors were able to prepare different 1H-1,2,3-triazole derivatives from a multicomponent reaction between benzyl chloride, sodium azide and different terminal alkynes with good yields.…”
Section: Main Sources Of Cu (Ii) Used In Cuaac Reactionsmentioning
confidence: 99%