Zobrazeno 1 - 10
of 16
pro vyhledávání: '"N. A. Kuprashvili"'
Publikováno v:
Pharmaceutical Chemistry Journal. 43:92-94
We have synthesized a series of new phenylazo derivatives of 1H,10H-benzo[e]pyrrolo[3, 2-g]indole containing 3-(p-bromophenylazo) (II), 3-(p-iodophenylazo) (III), 3-(p-sulfamidophenylazo) (IV), 3-formyl (V), 3,8-diformyl (VI), 3-phenylazo (VII), 3-(p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d31e2391b2b97e3ba5fbf1e31706f336
https://doi.org/10.1007/s11094-009-0245-8
https://doi.org/10.1007/s11094-009-0245-8
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:816-821
1H, 10H-benzo[e]pyrrolo[3,2-g]indole-2,9-dicarboxylic acid dichloride has been synthesized and condensed with amines and phenols to give the corresponding diamides and activated diesters. The mass spectra of the dichloride and several diamides have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba06350b3fe1e111f6e658b86c07be3d
https://doi.org/10.1007/bf02251689
https://doi.org/10.1007/bf02251689
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d970247f2aa4328555ed1e42bf72a00
https://doi.org/10.1002/chin.199526128
https://doi.org/10.1002/chin.199526128
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b469db1c94a5fe5235176ee8d6902be5
https://doi.org/10.1002/chin.199902118
https://doi.org/10.1002/chin.199902118
Publikováno v:
Chemistry of Heterocyclic Compounds. 24:489-493
1H,10H-Benzo[e]pyrrolo[3,2-g]indole reacts with the Vilsmeier and Mannich reagents to give disubstituted compounds, whereas monosubstitution products are formed in the case of diazo coupling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53fa72c402cb4737a1d34e17ea7a6c3b
https://doi.org/10.1007/bf00755686
https://doi.org/10.1007/bf00755686
Publikováno v:
Chemistry of Heterocyclic Compounds. 21:1016-1018
Cyclization of ethyl pyruvate 2,3-naphthylenehydrazone in polyphosphate ester gives 2,9-diethoxycarbonyl-1H,10H-benzo[e]pyrrolo[3,2-g]indole, which on hydrolysis and decarboxylation of the resulting acid affords the unsubtituted 1H,10H-benzo[e] pyrro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7878e0721a988c33622647cec966af0f
https://doi.org/10.1007/bf00515026
https://doi.org/10.1007/bf00515026
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f50bf6c2b22f0b41161f7f8911267180
https://doi.org/10.1002/chin.198852149
https://doi.org/10.1002/chin.198852149
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32f09112066aaa324eaef6a9ee362b55
https://doi.org/10.1002/chin.198607200
https://doi.org/10.1002/chin.198607200
Publikováno v:
Pharmaceutical Chemistry Journal. Feb2009, Vol. 43 Issue 2, p92-94. 3p. 1 Chart.
Autor:
Shetti, Vijayendra S.
Publikováno v:
Organic & Biomolecular Chemistry; 6/14/2022, Vol. 20 Issue 22, p4452-4470, 19p