Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M. G. Alapishvili"'
Autor:
E Kalandia, M. M. Matnadze, N. Z. Gakhokidze, M. G. Alapishvili, M. G. Maisuradze, S. P. Tsqvitaia, G Phalavandishvili
Publikováno v:
Chemical Science International Journal. 18:1-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f004621ac6a22aa335c7e75dcec96425
https://doi.org/10.9734/csji/2017/30939
https://doi.org/10.9734/csji/2017/30939
Autor:
G. A. Palavandishvili, M. G. Maisuradze, M. M. Matnadze, V. O. Ananiashvili, N. Z. Gakhokidze, M. G. Alapishvili
Publikováno v:
Chemistry of Heterocyclic Compounds. 48:1801-1804
Fusing 1,2-diaminodibenzothiophene dihydrochloride with urea and thiourea led to the formation of benzo[b]thiophene[3,2-e]benzimidazolone and benzo[b]thiophene[3,2-e]benzimidazolethione. 3H-Benzo-[b]thiophene[3,2-e]benzimidazole was used to obtain 3-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f27feb3ba99c2a2d33c654265468162
https://doi.org/10.1007/s10593-013-1211-7
https://doi.org/10.1007/s10593-013-1211-7
Autor:
M. M. Matnadze, N. Z. Gakhokidze, G. A. Palavandishvili, V. O. Ananiashvili, M. G. Alapishvili, M. G. Maisuradze
Publikováno v:
ChemInform. 44
Fusing 1,2-diaminodibenzothiophene dihydrochloride with urea and thiourea led to the formation of benzo[b]thiophene[3,2-e]benzimidazolone and benzo[b]thiophene[3,2-e]benzimidazolethione. 3H-Benzo-[b]thiophene[3,2-e]benzimidazole was used to obtain 3-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92af4159ecb846cbbf9445373680681e
https://doi.org/10.1002/chin.201343093
https://doi.org/10.1002/chin.201343093
Autor:
M. M. Matnadze, V. O. Ananiashvili, K. T. Batsikadze, L. N. Kurkovskaya, M. G. Alapishvili, I. G. Abesadze, T. O. Dzhashi, T. E. Khoshtariya, M. I. Sikharulidze
Publikováno v:
ChemInform. 38
A new method is described for the synthesis of the heterocyclic systems of benzo[b]thiophenoindoles from the respective isomeric amino acids with amino groups at positions 2 and 3. The method makes it possible to produce the tetracyclic systems with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6835c2bd0f1dd490e13027e190a62550
https://doi.org/10.1002/chin.200746222
https://doi.org/10.1002/chin.200746222
Autor:
M. G. Alapishvili, L. N. Kurkovskaya, M. I. Sikharulidze, V. O. Ananiashvili, I. G. Abesadze, T. O. Dzhashi, K. T. Batsikadze, M. M. Matnadze, E. T. Khoshtaria
Publikováno v:
ChemInform. 38
A new pathway has been proposed for the synthesis of dioxodihydro-1H-benzo[b]thiophenoindoles from the corresponding isomeric “amino acids” with amino groups at C(2) and C(3). This method yields these tetracyclic systems not only as a single isom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d2282be91348d0ea08aab2b35f35abc
https://doi.org/10.1002/chin.200704119
https://doi.org/10.1002/chin.200704119
Autor:
G. V. Popova, M. V. Milashvili, N. N. Suvorov, E. D. Vorontsov, M. G. Alapishvili, E. V. Ivanova, Vyacheslav V. Kireev
Publikováno v:
Chemistry of Heterocyclic Compounds. 19:398-401
A number of cyclotriphosphazenes monosubstituted with tryptamine residues were synthesized. The conditions for the aminolysis of hexachlorocyclotriphosphazene with tryptamine, 5-nitrotryptamine, and 5-benzyloxytryptamine were examined. The physicoche
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5b2da1593afb56f05ceaf9647dd9f38
https://doi.org/10.1007/bf00516207
https://doi.org/10.1007/bf00516207
Autor:
E. D. Vorontsov, Vyacheslav V. Kireev, M. G. Alapishvili, N. N. Suvorov, E. V. Ivanova, M. V. Milashvili, G. V. Popova
Publikováno v:
Chemischer Informationsdienst. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dab0a7f4dabeae24e12be35be5f5b54c
https://doi.org/10.1002/chin.198339279
https://doi.org/10.1002/chin.198339279