EventsThe 18th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 18th International Electronic Conference on Synthetic Organic Chemistry
Published date
31 Oct, 2014
Citation
Andrei Khlebnikov, Andrei Potapov, Nina Chernova, Tolebi Dzhienalyev, Synthesis of Pyrazole-Derived Dithioethers Using in situ Generation of Dithiolate-Ions, in Proceedings of The 18th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2014, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-18-a010
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Synthesis of Pyrazole-Derived Dithioethers Using in situ Generation of Dithiolate-Ions

Nina Chernova 1
image
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Andrei Khlebnikov 1,2
1. Altai State Technical University
2. National Research Tomsk Polytechnic University
Abstract
A number of pyrazole-derived dithioethers were prepared by the reaction of diisothiuronium salts and 2-(3,5-dimethylpyrazol-1-yl)ethanol tosylate in a basic aqueous solution. Diisothiuronium salts were prepared by the reaction of thiourea with alpha,omega-dibromoalkanes containing from three to twelve methylene groups. The use of these salts allowed in situ generation of dithiolate ions, thus eliminating the need to use hazardous dimercaptanes.
Keywords
Pyrazole
thioether ligands
thiourea
thiuronium salts
Manuscript
Poster
potapov.pdf
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