Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Andrey Galustyan"'
Autor:
Daria A. Burmistrova, Andrey Galustyan, Nadezhda P. Pomortseva, Kristina D. Pashaeva, Maxim V. Arsenyev, Oleg P. Demidov, Mikhail A. Kiskin, Andrey I. Poddel’sky, Nadezhda T. Berberova, Ivan V. Smolyaninov
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 2378-2391 (2024)
A series of new RS−, RS−CH2− and R2N−CH2-functionalized сatechols with heterocyclic fragments such as 1,3,4-oxadiazole, 1,2,4-triazole, thiazole, or pyridine were synthesized by the reaction of 3,5-di-tert-butyl-o-benzoquinone or 3,5-di-tert
Externí odkaz:
https://doaj.org/article/0e7cbdabb2fe425c9582c25afa879309
Publikováno v:
Journal of The Electrochemical Society. 169:116501
Two approaches to synthesis of unsymmetrical disulfides based on different types of thiol activation, namely, an electrochemical method in the presence of a redox mediator and a microwave irradiation, were discussed. The mediated electrosynthesis pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea9003bfd58c8c738dff1ec827337ff6
https://doi.org/10.1149/1945-7111/ac9d69
https://doi.org/10.1149/1945-7111/ac9d69
Publikováno v:
Journal of The Electrochemical Society. 168:055501
A number of substituted o-aminophenols has been investigated as redox mediators of the thiol oxidation to disulfides. The electrooxidation of o-aminophenols leads to the corresponding o-iminobenzoquinones. These compounds react with thiols in the sol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21aa40c08d4aa090ce9b7b8633bdd50b
https://doi.org/10.1149/1945-7111/abfe43
https://doi.org/10.1149/1945-7111/abfe43