Results 321 to 330 of about 44,050 (359)
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Journal of Organic Chemistry, 2017
An efficient chemoselective practical route to fully substituted thiazoles and 2,3-dihydrothiazoles has been devised by [4 + 1] heterocyclization of α-(N-hydroxy/aryl)imino-β-oxodithioesters with in situ generated Cu-carbenoids of diazocarbonyls.
Abhijeet Srivastava+3 more
semanticscholar +1 more source
An efficient chemoselective practical route to fully substituted thiazoles and 2,3-dihydrothiazoles has been devised by [4 + 1] heterocyclization of α-(N-hydroxy/aryl)imino-β-oxodithioesters with in situ generated Cu-carbenoids of diazocarbonyls.
Abhijeet Srivastava+3 more
semanticscholar +1 more source
, 2016
Heating of commercially available styrenes with NBS in water followed by reaction with 2-aminopyridines or thioamides afforded important heterocyclic scaffolds in a one pot procedure.
M. Shinde, Umesh A. Kshirsagar
semanticscholar +1 more source
Heating of commercially available styrenes with NBS in water followed by reaction with 2-aminopyridines or thioamides afforded important heterocyclic scaffolds in a one pot procedure.
M. Shinde, Umesh A. Kshirsagar
semanticscholar +1 more source
Synthesis of Condensed Thiazoles
ChemInform, 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.
N. G. Smirnova+2 more
openaire +2 more sources
, 2016
The development of a visible light promoted, mild and greener approach for the synthesis of highly functionalized thiazoles and imidazo[2,1-b]thiazoles under photochemical activation in EtOH : H2O green medium is demonstrated.
A. Mishra+6 more
semanticscholar +1 more source
The development of a visible light promoted, mild and greener approach for the synthesis of highly functionalized thiazoles and imidazo[2,1-b]thiazoles under photochemical activation in EtOH : H2O green medium is demonstrated.
A. Mishra+6 more
semanticscholar +1 more source
Journal für Praktische Chemie, 1967
AbstractDas aus Xanthanwasserstoff bzw. Cyanamid und Schwefelkohlenstoff erhältliche Cyanamido‐dithiocarbonat reagiert mit Halogenessigsäurederivaten sowie mit Chlormethylketonen unter S‐Alkylierung und gleichzeitiger Cyclisierung zu 4‐Aminothiazolderivaten.
P. Blauschmidt, K. Gewald, R. Mayer
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AbstractDas aus Xanthanwasserstoff bzw. Cyanamid und Schwefelkohlenstoff erhältliche Cyanamido‐dithiocarbonat reagiert mit Halogenessigsäurederivaten sowie mit Chlormethylketonen unter S‐Alkylierung und gleichzeitiger Cyclisierung zu 4‐Aminothiazolderivaten.
P. Blauschmidt, K. Gewald, R. Mayer
openaire +2 more sources
K2S2O8-Promoted Direct C–H Phosphorylation of (Benzo)thiazoles
, 2017The direct phosphorylation of (benzo)thiazoles with various H-phosphine oxides was realized by using K2S2O8 as the oxidant. A series of 2-phosphoryl (benzo)thiazoles were obtained in moderate to good yields.
Weidong Lin+3 more
semanticscholar +1 more source
Design, Synthesis, and Characterization of Some New bis‐thiazoles
, 2017The essential idea of the work in this article is mainly dependent on the use of bis-hydrazonoyl halides for heterocyclic synthesis. The present work describes preparation and characterization of new bis-thiazoles from reaction of bis-hydrazonoyl ...
Sobhi M. Gomha, T. Farghaly, A. R. Sayed
semanticscholar +1 more source
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
openaire +2 more sources
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
openaire +2 more sources
2008
[79265-30-8] C6H11NSSi (MW 157.34) InChI = 1S/C6H11NSSi/c1-9(2,3)6-7-4-5-8-6/h4-5H,1-3H3 InChIKey = VJCHUDDPWPQOLH-UHFFFAOYSA-N (useful formyl anion equivalent;1 effective one-carbon homologating reagent of alkoxy aldehydes, amino aldehydes, and dialdoses2) Physical Data: bp 51–53 °C/10 mmHg; d 0.992 g mL−1; nD 1.4980.
María M. Zarzuelo+4 more
openaire +2 more sources
[79265-30-8] C6H11NSSi (MW 157.34) InChI = 1S/C6H11NSSi/c1-9(2,3)6-7-4-5-8-6/h4-5H,1-3H3 InChIKey = VJCHUDDPWPQOLH-UHFFFAOYSA-N (useful formyl anion equivalent;1 effective one-carbon homologating reagent of alkoxy aldehydes, amino aldehydes, and dialdoses2) Physical Data: bp 51–53 °C/10 mmHg; d 0.992 g mL−1; nD 1.4980.
María M. Zarzuelo+4 more
openaire +2 more sources