Azaheterocycles Based on Α, Β-Unsaturated Carbonyls
DOI: 10.1007/978-3-540-68367-4_1
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Cited by 11 publications
(15 citation statements)
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“…The Lewis acid catalyst activates the carbonyl group in salicylaldehyde ( 2 ), which is subsequently able to interact with the 4-CH nucleophilic center of the aminoisoxazole 1 and not only with the exocyclic NH 2 group [26]. The resulting adduct 10 (Scheme 4, pathway C) then reacts with carboxamide 3a forming intermediate 11 which can lose a water molecule in two different ways: either by elimination occurring at room temperature leading to dihydroisoxazolo[5,4- b ]pyridine 5a or through nucleophilic substitution involving the phenolic hydroxy group under ultrasonic activation furnishing the oxygen-bridged compound 6a .…”
Section: Resultsmentioning
confidence: 99%
“…The Lewis acid catalyst activates the carbonyl group in salicylaldehyde ( 2 ), which is subsequently able to interact with the 4-CH nucleophilic center of the aminoisoxazole 1 and not only with the exocyclic NH 2 group [26]. The resulting adduct 10 (Scheme 4, pathway C) then reacts with carboxamide 3a forming intermediate 11 which can lose a water molecule in two different ways: either by elimination occurring at room temperature leading to dihydroisoxazolo[5,4- b ]pyridine 5a or through nucleophilic substitution involving the phenolic hydroxy group under ultrasonic activation furnishing the oxygen-bridged compound 6a .…”
Section: Resultsmentioning
confidence: 99%
“…Azolopyrimidines having a nodal nitrogen are excellent objects for both, either multicomponent [2] or sequential synthesis [3] (Scheme 1); both of them presume use of diverse aminoazoles 1 (3-amino-1,2,4-triazole [4], 3-aminopyrazole [5], 5-aminotetrazole [6] Another important trend in modern synthesis is "green chemistry" [7]; among its principles use of "green" solvents like water appeared to be highly effective [8].…”
Section: Introductionmentioning
confidence: 99%
“…It should be noted that multicomponent reactions, involving simultaneous interaction of, at least, three compounds and forming one final product together with parts of all the initial components, contribute to the development of new methods to synthesize polyfunctional carbo-and hetero-cycles with useful properties. Typically, the developed multicomponent reactions proceed in one-step ("one-pot"), by using commercially available substrates and reagents, which significantly reduce the cost of final products as well as harmful environmental consequences of the synthesis occurrence [1][2][3][4][5]. A large number of multicomponent reactions have been discovered, analyzed and described.…”
Section: Introductionmentioning
confidence: 99%