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Alpha-Haloketone
The Experts below are selected from a list of 15 Experts worldwide ranked by ideXlab platform
Hugo Cerecetto – 1st expert on this subject based on the ideXlab platform
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A serendipitous one-step conversion of 3H-1,2-dithiole-3-thione to (E)-3-[1-(alkylthio)alkylidene]-3H-1,2-dithiole: an experimental and theoretical study
Molecular Diversity, 2014Co-Authors: Marcos Couto, Mauricio Cabrera, Gustavo A. Echeverría, Oscar E. Piro, Mercedes González, Hugo CerecettoAbstract:In the course of our studies on 3 $$H$$ H -1,2-dithiole-3-thione synthesis, a serendipitous reactivity with $$\alpha $$ α -haloketones, in the presence of excess of potassium iodide, has been observed. Instead of the expected reaction of the nucleophile in a remote point of the molecule, we have obtained a product resulted from the electrophile character of the thiocarbonyl moiety on the 3-position of the 1,2-dithiole. In order to obtain an efficient protocol in terms of energy efficiency, this methodology was studied under conventional and microwave heating with similar or better results in the latter conditions. Simplicity and great efficiency in this one-step transformation are some of the advantages of this reaction. Moreover, the results can be explained according to the Pearson’s hard and soft acid base theory.
Marcos Couto – 2nd expert on this subject based on the ideXlab platform
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A serendipitous one-step conversion of 3H-1,2-dithiole-3-thione to (E)-3-[1-(alkylthio)alkylidene]-3H-1,2-dithiole: an experimental and theoretical study
Molecular Diversity, 2014Co-Authors: Marcos Couto, Mauricio Cabrera, Gustavo A. Echeverría, Oscar E. Piro, Mercedes González, Hugo CerecettoAbstract:In the course of our studies on 3 $$H$$ H -1,2-dithiole-3-thione synthesis, a serendipitous reactivity with $$\alpha $$ α -haloketones, in the presence of excess of potassium iodide, has been observed. Instead of the expected reaction of the nucleophile in a remote point of the molecule, we have obtained a product resulted from the electrophile character of the thiocarbonyl moiety on the 3-position of the 1,2-dithiole. In order to obtain an efficient protocol in terms of energy efficiency, this methodology was studied under conventional and microwave heating with similar or better results in the latter conditions. Simplicity and great efficiency in this one-step transformation are some of the advantages of this reaction. Moreover, the results can be explained according to the Pearson’s hard and soft acid base theory.
Mercedes González – 3rd expert on this subject based on the ideXlab platform
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A serendipitous one-step conversion of 3H-1,2-dithiole-3-thione to (E)-3-[1-(alkylthio)alkylidene]-3H-1,2-dithiole: an experimental and theoretical study
Molecular Diversity, 2014Co-Authors: Marcos Couto, Mauricio Cabrera, Gustavo A. Echeverría, Oscar E. Piro, Mercedes González, Hugo CerecettoAbstract:In the course of our studies on 3 $$H$$ H -1,2-dithiole-3-thione synthesis, a serendipitous reactivity with $$\alpha $$ α -haloketones, in the presence of excess of potassium iodide, has been observed. Instead of the expected reaction of the nucleophile in a remote point of the molecule, we have obtained a product resulted from the electrophile character of the thiocarbonyl moiety on the 3-position of the 1,2-dithiole. In order to obtain an efficient protocol in terms of energy efficiency, this methodology was studied under conventional and microwave heating with similar or better results in the latter conditions. Simplicity and great efficiency in this one-step transformation are some of the advantages of this reaction. Moreover, the results can be explained according to the Pearson’s hard and soft acid base theory.