Zobrazeno 1 - 7
of 7
pro vyhledávání: '"N. N. Nikoleishvili"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:540-544
The Vilsmeier formylation of bifunctional Fischer base analogs in the dipyrrolobenzoquinoxaline and indoloindole series was studied with various substrate–Vilsmeier complex ratios. The isomeric Fischer bases of the indoloindole series were formylat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e476b1e3f6707557bc1f9c349143bb8
https://doi.org/10.1007/s10593-013-1279-0
https://doi.org/10.1007/s10593-013-1279-0
Autor:
N. N. Nikoleishvili, Uli Kazmaier, K. G. Japaridze, Sh. A. Samsoniya, M. V. Trapaidze, J. P. Maisuradze
Publikováno v:
Chemistry of Heterocyclic Compounds. 47:1098-1104
The synthesis of new condensed indoline bis-spiropyrans from isomeric hexamethyldihydroindolo-[4,5-e]-and -[7,6-g]indoles, and also from hexamethyldihydrobenzo[e]pyrrolo[3,2-g]indole in three stages has been generalized. By condensation of the isomer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ebf38797da2fdaf767548e378858775
https://doi.org/10.1007/s10593-011-0880-3
https://doi.org/10.1007/s10593-011-0880-3
Autor:
M. V. Trapaidze, N. N. Nikoleishvili, J. P. Maisuradze, Sh. A. Samsoniya, Uli Kazmaier, K. G. Japaridze
Publikováno v:
Chemistry of Heterocyclic Compounds. 46:1016-1019
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::033786ab4a26648505056e7c86684b95
https://doi.org/10.1007/s10593-010-0618-7
https://doi.org/10.1007/s10593-010-0618-7
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::903a5b2be1420f4495fc7461802a5654
https://doi.org/10.1002/chin.201403128
https://doi.org/10.1002/chin.201403128
Autor:
J. P. Maisuradze, Uli Kazmaier, K. G. Japaridze, Sh. A. Samsoniya, N. N. Nikoleishvili, M. V. Trapaidze
Publikováno v:
Chemistry of Heterocyclic Compounds. 46:1020-1022
In previous work [1], we reported the synthesis of spirocyclic dihydroindolizine systems derived from 2,3,3,8,9,9-hexamethyl-3,8-dihydrobenzo[e]pyrrolo[3,2-g]indole (1). In a continuation of work on the synthesis of bisspiro compounds, we report the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f9b246fffbf9adcc2d00f430ca8e597
https://doi.org/10.1007/s10593-010-0619-6
https://doi.org/10.1007/s10593-010-0619-6
Publikováno v:
Chemistry of Heterocyclic Compounds. 44:1016-1018
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a016b5e6ded3098ef5de2a7d5123e0e0
https://doi.org/10.1007/s10593-008-0149-7
https://doi.org/10.1007/s10593-008-0149-7
Autor:
Sh. A. Samsoniya, N. N. Nikoleishvili, M. V. Trapaidze, K. G. Japaridze, Uli Kazmaier, J. P. Maisuradze
Publikováno v:
ChemInform. 43
The synthesis of new condensed indoline bis-spiropyrans from isomeric hexamethyldihydroindolo-[4,5-e]-and -[7,6-g]indoles, and also from hexamethyldihydrobenzo[e]pyrrolo[3,2-g]indole in three stages has been generalized. By condensation of the isomer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9daa3b93528fc76fb68e619c7b455f7c
https://doi.org/10.1002/chin.201219142
https://doi.org/10.1002/chin.201219142