Zobrazeno 1 - 10
of 11
pro vyhledávání: '"V. O. Ananiashvili"'
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:
T. O. Dzhashi, M. M. Matnadze, T. E. Khoshtariya, K. T. Batsikadze, V. O. Ananiashvili, M. I. Sikharulidze, L. N. Kurkovskaya
Publikováno v:
Chemistry of Heterocyclic Compounds. 43:1239-1246
A new method is described for the synthesis of the 1H-benzo[b]furoindole heterocyclic systems from the corresponding isomeric amino acids with amino groups at positions 2 and 3. By this method it is possible to obtain these tetracyclic systems not on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f98921e50b9a19b9aa57404e76a0ab9a
https://doi.org/10.1007/s10593-007-0189-4
https://doi.org/10.1007/s10593-007-0189-4
Autor:
M. M. Matnadze, M. I. Sikharulidze, K. T. Batsikadze, V. O. Ananiashvili, L. N. Kurkovskaya, T. E. Khoshtariya, T. O. Dzhashi
Publikováno v:
Chemistry of Heterocyclic Compounds. 43:1111-1117
A new method for the synthesis of the dioxodihydro-1H-benzo[b]furoindole heterocyclic systems from the corresponding isomeric amino acids with the amino groups at positions 2 and 3 is described. By this method it is possible not only to obtain the in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::361ba585abef014993019f28bb07230a
https://doi.org/10.1007/s10593-007-0171-1
https://doi.org/10.1007/s10593-007-0171-1
Autor:
M. I. Sikharulidze, T. E. Khoshtariya, L. T. Bochoidze, V. O. Ananiashvili, V. G. Turabelidze, N. T. Mirziashvili, M. G. Maisuradze, I. G. Abesadze, T. O. Dzhashi, L. N. Kurkovskaya, K. T. Batsikadze
Publikováno v:
Chemistry of Heterocyclic Compounds. 41:208-215
A preparative route is proposed for the synthesis of the novel heterocyclic systems 7-oxo- and 1,2,7-trioxo-1,2-dihydropyrano[3,2-e]indole using classical Fischer and Sandmeyer methods respectively. We have studied various conditions for cyclization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49596de893cd96c15fcc548c8d365af6
https://doi.org/10.1007/s10593-005-0129-0
https://doi.org/10.1007/s10593-005-0129-0
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
Publikováno v:
ChemInform. 44
Two new tetracyclic heterocompounds are obtained by cyclization under modified Phillips conditions within short reaction times.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11e0597f6badfc9e7cb4ec2f40edaab3
https://doi.org/10.1002/chin.201313105
https://doi.org/10.1002/chin.201313105
Autor:
T. E. Khoshtariya, L. N. Kurkovskaya, T. O. Dzhashi, V. O. Ananiashvili, K. T. Batsikadze, M. I. Sikharulidze, M. M. Matnadze
Publikováno v:
ChemInform. 39
A new method for the synthesis of the dioxodihydro-1H-benzo[b]furoindole heterocyclic systems from the corresponding isomeric amino acids with the amino groups at positions 2 and 3 is described. By this method it is possible not only to obtain the in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::057e9c7e8c82769ae9787d45d4e67f35
https://doi.org/10.1002/chin.200817121
https://doi.org/10.1002/chin.200817121
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:
T. E. Khoshtariya, L. N. Kurkovskaya, L. T. Bochoidze, K. T. Batsikadze, N. T. Mirziashvilli, I. G. Abesadze, M. I. Sikharulidze, V. G. Turabelidze, V. O. Ananiashvili, T. O. Dzhashi, et al. et al.
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::332e0e638e00787205c8dd0eb06979d7
https://doi.org/10.1002/chin.200602127
https://doi.org/10.1002/chin.200602127