2013
DOI: 10.13005/ojc/290448
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Microwave-Assisted One-Step Synthesis of 2,5-Disubstituted-1,3,4-Oxadiazoles Using 1,4- Bis(triphenylphosphonium)-2-Butene Peroxodisulfate

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Cited by 5 publications
(2 citation statements)
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“…Gorjizadeh et al reported the efficient synthesis of a series of 1,3,4-oxadiazoles ( 3 ) from the cyclization–oxidation reaction of acyl hydrazones ( 1 ) with substituted aldehydes ( 2 ) by using 1,4-bis(triphenylphosphonium)-2-butene peroxodisulfate (BTPPDS) as an oxidant in a solvent-free medium under microwave irradiation ( Scheme 3 ). The reaction was found to proceed smoothly under microwave irradiation within 25 min, whereas 12 h were required to complete the reaction under reflux conditions [ 21 ].…”
Section: Chemistry Of Oxadiazolemoietymentioning
confidence: 99%
“…Gorjizadeh et al reported the efficient synthesis of a series of 1,3,4-oxadiazoles ( 3 ) from the cyclization–oxidation reaction of acyl hydrazones ( 1 ) with substituted aldehydes ( 2 ) by using 1,4-bis(triphenylphosphonium)-2-butene peroxodisulfate (BTPPDS) as an oxidant in a solvent-free medium under microwave irradiation ( Scheme 3 ). The reaction was found to proceed smoothly under microwave irradiation within 25 min, whereas 12 h were required to complete the reaction under reflux conditions [ 21 ].…”
Section: Chemistry Of Oxadiazolemoietymentioning
confidence: 99%
“…Among the different organophos-phorics, trialkyl phosphates, PO(OR) 3 , that are produced in important amount, are noticeably relevant and are widely employed in different technological areas as extractors of rare and radioactive elements, inhibitors of metal corrosion and polymer burning, additives to combustible and lubricating materials, brake-liquids, etc 4-6 . Other secondary reactions are possible, know the condensation reaction which from monophosphates forms pyrophosphates (Scheme 3).…”
mentioning
confidence: 99%