Reactions of 3-(3-chloroprop-2-en-1-ylsulfanyl)- and 3-(prop-2-yn-1-ylsulfanyl)-5 H -[1,2,4]triazino[5,6- b ]indoles with halogens

Verfasser / Beitragende:
[A. Rybakova, D. Kim, M. Ezhikova, M. Kodess]
Ort, Verlag, Jahr:
2015
Enthalten in:
Russian Journal of Organic Chemistry, 51/7(2015-07-01), 1016-1019
Format:
Artikel (online)
ID: 605529396
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024 7 0 |a 10.1134/S1070428015070209  |2 doi 
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245 0 0 |a Reactions of 3-(3-chloroprop-2-en-1-ylsulfanyl)- and 3-(prop-2-yn-1-ylsulfanyl)-5 H -[1,2,4]triazino[5,6- b ]indoles with halogens  |h [Elektronische Daten]  |c [A. Rybakova, D. Kim, M. Ezhikova, M. Kodess] 
520 3 |a 3-(3-Chloroprop-2-en-1-ylsulfanyl)- and 3-(prop-2-yn-1-ylsulfanyl)-5H-[1,2,4]triazino[5,6-b]indoles reacted with iodine and bromine to give derivatives of 2,3-dihydro-10H-[1,3]thiazolo[3′,2′: 2,3][1,2,4]-triazino[5,6-b]indolium halides whose structure was determined by 1H and 13C NMR spectroscopy using twodimensional 1H-1H COSY, 1H-13C HSQC, and 1H-13C HMBC techniques. 
540 |a Pleiades Publishing, Ltd., 2015 
700 1 |a Rybakova  |D A.  |u National Research South Ural State University, pr. imeni V.I. Lenina 76, 454080, Chelyabinsk, Russia  |4 aut 
700 1 |a Kim  |D D.  |u National Research South Ural State University, pr. imeni V.I. Lenina 76, 454080, Chelyabinsk, Russia  |4 aut 
700 1 |a Ezhikova  |D M.  |u Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, ul. S. Kovalevskoi/Akademicheskaya 22/20, 620990, Yekaterinburg, Russia  |4 aut 
700 1 |a Kodess  |D M.  |u Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, ul. S. Kovalevskoi/Akademicheskaya 22/20, 620990, Yekaterinburg, Russia  |4 aut 
773 0 |t Russian Journal of Organic Chemistry  |d Pleiades Publishing  |g 51/7(2015-07-01), 1016-1019  |x 1070-4280  |q 51:7<1016  |1 2015  |2 51  |o 11178 
856 4 0 |u https://doi.org/10.1134/S1070428015070209  |q text/html  |z Onlinezugriff via DOI 
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900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
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950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1134/S1070428015070209  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Rybakova  |D A.  |u National Research South Ural State University, pr. imeni V.I. Lenina 76, 454080, Chelyabinsk, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kim  |D D.  |u National Research South Ural State University, pr. imeni V.I. Lenina 76, 454080, Chelyabinsk, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ezhikova  |D M.  |u Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, ul. S. Kovalevskoi/Akademicheskaya 22/20, 620990, Yekaterinburg, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kodess  |D M.  |u Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, ul. S. Kovalevskoi/Akademicheskaya 22/20, 620990, Yekaterinburg, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Russian Journal of Organic Chemistry  |d Pleiades Publishing  |g 51/7(2015-07-01), 1016-1019  |x 1070-4280  |q 51:7<1016  |1 2015  |2 51  |o 11178