Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Alexander Yu. Makarov"'
Autor:
Leonid A. Shundrin, Irina G. Irtegova, Pavel A. Avrorov, Tatiana F. Mikhailovskaya, Arkady G. Makarov, Alexander Yu. Makarov, Andrey V. Zibarev
Publikováno v:
ARKIVOC, Vol 2017, Iss 3, Pp 166-180 (2017)
Externí odkaz:
https://doaj.org/article/67ffeb9670264d0090b7449c9ad74afc
Autor:
Alexander Yu. Makarov, Yulia M. Volkova, Samat B. Zikirin, Irina G. Irtegova, Irina Yu. Bagryanskaya, Yuri V. Gatilov, Andrey A. Nefedov, Andrey V. Zibarev
Publikováno v:
New Journal of Chemistry. 46:3687-3696
3,1,2,4-Benzothiaselenadiazines, 1,3,2,4-benzodithiadiazines and 1,2,4,3,5-benzotrithiadiazepines are synthesized from Ar–NSN–SiMe3 and chalcogen chlorides, and converted into Herz salts, radicals and molecular complexes, and S- and Se-Bunt
Publikováno v:
Applied Magnetic Resonance. 41:449-466
This paper gives a brief overview of a new approach to chalcogen–nitrogen heterocyclic π-radicals, particularly 1,2,3- and 1,3,2-benzodithiazolyls, based on thermolysis or photolysis of closed-shell precursors (such as 1,3,2,4-benzodithiadiazines
Autor:
A. S. Knyazev, Andrey V. Zibarev, Irina Yu. Bagryanskaya, Alexander Yu. Makarov, Yuri G. Slizhov, Arkady G. Makarov, Natalia Yu. Selikhova, Yuri V. Gatilov, V.S. Malkov
Publikováno v:
ChemInform. 46
Useful synthetic approaches for the preparation of fluorinated 1,2-diaminoarenes, quinoxalines, 2,1,3-arenothia(selena)diazoles and related compounds starting from corresponding fluorinated anilines (I) are elaborated.
Autor:
Andrey V. Zibarev, Natalia Yu. Selikhova, Yuri G. Slizhov, Yuri V. Gatilov, Irina Yu. Bagryanskaya, A. S. Knyazev, V.S. Malkov, Arkady G. Makarov, Alexander Yu. Makarov
Publikováno v:
Journal of fluorine chemistry. 2014. Vol. 165. P. 123-131
5,6,7,8-Tetrafluoroquinoxaline (1) and its previously unknown derivatives (2–8) were synthesized from glyoxal and polyfluorinated 1,2-diaminoarenes (10–17) obtained by reduction of corresponding 2,1,3-arenothiadiazoles (including new ones 21 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6f27663645cc1aeb2bffe0ede80503d
http://vital.lib.tsu.ru/vital/access/manager/Repository/vtls:000490269
http://vital.lib.tsu.ru/vital/access/manager/Repository/vtls:000490269
Autor:
Yuri V. Gatilov, Irina Yu. Bagryanskaya, Makhmut M. Shakirov, Alexander Yu. Makarov, Andrey V. Zibarev
Publikováno v:
Mendeleev Communications. 13:19-21
Fluoro-containing 1,3λ4δ2,2,4-benzodithiadiazines 2–4 unexpectedly add water to give previously unknown 2-amino-N-sulfinylbenzenesulfenamides 5–7 as the first derivatives of still undescribed 2-aminobenzenesulfenamide 10.
Publikováno v:
ChemInform. 43
This paper gives a brief overview of a new approach to chalcogen–nitrogen heterocyclic π-radicals, particularly 1,2,3- and 1,3,2-benzodithiazolyls, based on thermolysis or photolysis of closed-shell precursors (such as 1,3,2,4-benzodithiadiazines
Publikováno v:
ChemInform. 39
This review highlights the most important advances in the heteroatom chemistry of 1,3,2,4-benzodithiadiazines (π-excessive and formally antiaromatic heterocycles), covering methods for synthesis, nontrivial features of the molecular and π-electroni
Autor:
Nina P. Gritsan, Elena A. Pritchina, Thomas Bally, Andrey V. Zibarev, and Alexander Yu. Makarov
Photolysis of 1,3,2,4-benzodithiadiazine (1) at ambient temperature yields stable 1,2,3-benzodithiazolyl radicals. In order to reveal the mechanism of this unusual transformation, the photochemistry of 1 was studied in argon matrices using IR and UV-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09fcdd5ba2067e51fba438a9a481682c
http://doc.rero.ch/record/8846/files/bally_mic.pdf
http://doc.rero.ch/record/8846/files/bally_mic.pdf
Publikováno v:
European journal of inorganic chemistry
This review highlights the most important advances in the heteroatom chemistry of 1,3,2,4-benzodithiadiazines (π-excessive and formally antiaromatic heterocycles), covering methods for synthesis, nontrivial features of the molecular and π-electroni