2012
DOI: 10.1016/j.tetlet.2012.05.062
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Catalysis by zeolite leading to the construction of thiazole ring: an improved synthesis of 4-alkynyl substituted thiazoles

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Cited by 10 publications
(3 citation statements)
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“…The main advantages of this methodology are the absence of solvents to perform the reaction, an inexpensive catalyst, and mild reaction conditions. Zeolites are microporous crystalline aluminosilicates built from inifinitely extending a three-dimensional network of SiO 4 and AlO 4 tetrahedra that are linked together through oxygen bridges. By virtue of their structure, crystallinity, and variable stiochiometry, zeolite catalysts have well-defined pore size distributions, adjustable acidity, very high surface area, and good thermal stability .…”
Section: Introductionmentioning
confidence: 99%
“…The main advantages of this methodology are the absence of solvents to perform the reaction, an inexpensive catalyst, and mild reaction conditions. Zeolites are microporous crystalline aluminosilicates built from inifinitely extending a three-dimensional network of SiO 4 and AlO 4 tetrahedra that are linked together through oxygen bridges. By virtue of their structure, crystallinity, and variable stiochiometry, zeolite catalysts have well-defined pore size distributions, adjustable acidity, very high surface area, and good thermal stability .…”
Section: Introductionmentioning
confidence: 99%
“…Scalacci et al [28] developed a microwave-assisted protocol for the preparation of thiazoles (39) and thiazolines (40) in high yields using catalytic PTSA (p-Toluenesulfonic acid). At higher temperatures, a mixture of compounds (39 and 40) was observed in the presence of base (Scheme 12).…”
Section: Isothiocyanatesmentioning
confidence: 99%
“…Arunkumar and coworkers [40] developed the Zeolite H-beta mediated preparation of 2-methyl-4-[(trimethylsilyl)ethynyl] thiazole (80). This product served as a vital synthon and was used in Sonogashira coupling [41] to yield 4-alkynyl substituted thiazole derivatives (Scheme 25).…”
Section: Thioamidesmentioning
confidence: 99%