Results 161 to 170 of about 9,794 (211)
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The Thiazole Aldehyde Synthesis
Synthesis, 1998Aldehydes with diverse structural arrays are prepared by construction of carbon chains at C-2 of the thiazole ring and conversion of the heterocycle into the formyl group. Various methods are described that differ depending on the type of thiazole-based reagent employed in the initial carbon-carbon bond forming reaction leading to 2-substituted ...
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Direct Arylation of Thiazoles on Water
Angewandte Chemie, 2007Wetter is better: The direct arylation of thiazoles on water is quicker, cleaner, and higher-yielding than arylation in organic solvents. The reaction works under mild conditions for an array of aryl iodides, producing 2,5-diaryl thiazoles in excellent yields.
Turner, Gemma L. +2 more
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Imidazole, oxazole and thiazole alkaloids
Natural Product Reports, 2006AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
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Synthesis of Oligonucleotides Containing Thiazole and Thiazole N-Oxide Nucleobases
Organic Letters, 2002[reaction: see text] The thiazole C-nucleoside analogue was synthesized by the Hantzsch cyclization method to form the thiazole ring and was then converted to the thiazole N-oxide C-nucleoside analogue by peracid oxidation of the heterocycle nitrogen.
Tod J, Miller +6 more
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Journal of Pharmaceutical Sciences, 1978
The homolytic arylation of thiazole with phenylazotriphenylmethane (as a free radical source) was carried out to explore the potential chemotherapeutic activity of the resulting triphenylmethyl derivatives. The experimental data differed from similar results on other isosteric heterocycles: one compound only was obtained, having both phenyl and ...
G, Fenech, A, Chimirri, R, Ficarra
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The homolytic arylation of thiazole with phenylazotriphenylmethane (as a free radical source) was carried out to explore the potential chemotherapeutic activity of the resulting triphenylmethyl derivatives. The experimental data differed from similar results on other isosteric heterocycles: one compound only was obtained, having both phenyl and ...
G, Fenech, A, Chimirri, R, Ficarra
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2012
This chapter highlights the recent developments in the metalation of thiazoles and benzothiazoles as well as the reactions of the resulting metalated species (2000 to present). Metalation reactions consist of lithiation (including halogen dance reactions), magnesation, zincation, caldation, boronation, and silylation, while application of the metalated
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This chapter highlights the recent developments in the metalation of thiazoles and benzothiazoles as well as the reactions of the resulting metalated species (2000 to present). Metalation reactions consist of lithiation (including halogen dance reactions), magnesation, zincation, caldation, boronation, and silylation, while application of the metalated
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Future Medicinal Chemistry
Aim: Novel thiazole hybrids were synthesized via thiazolation of 4-phenylthiosemicarbazone (4). Materials & methods: The anticancer activity against the NCI 60 cancer cell line panel. Results: Methyl 2-(2-((1-(naphthalen-2-yl)ethylidene)hydrazineylidene)-4-oxo-3-phenylthiazolidin-5-ylidene)acetate (6a) showed significant anticancer activity at 10 μM ...
Walid E Elgammal +8 more
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Aim: Novel thiazole hybrids were synthesized via thiazolation of 4-phenylthiosemicarbazone (4). Materials & methods: The anticancer activity against the NCI 60 cancer cell line panel. Results: Methyl 2-(2-((1-(naphthalen-2-yl)ethylidene)hydrazineylidene)-4-oxo-3-phenylthiazolidin-5-ylidene)acetate (6a) showed significant anticancer activity at 10 μM ...
Walid E Elgammal +8 more
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Synthesis of Thiazoles from Metalated Thiazoles
2010P. A. Koutentis, H. A. Ioannidou
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