Zobrazeno 1 - 6
of 6
pro vyhledávání: '"N. S. Masterova"'
Autor:
S. S. Kiselev, M. I. Evstratova, L. M. Alekseeva, N. S. Masterova, Vladimir G Granik, S. Yu. Ryabova
Publikováno v:
Russian Chemical Bulletin. 59:637-641
Acid treatment of β-(3-acetoxyindol-2-yl)-α-cyanoacrylic acid derivatives (ethyl ester and nitrile) with aqueous or gaseous HCl afforded novel 3-substituted 2-oxo-2,5-dihydropyra-no[3,2-b]indoles. 2-Oxo-2,5-dihydropyrano[3,2-b]indole-3-carbonitrile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a151f7834e6d0bbeb5ccbdaa3381586
https://doi.org/10.1007/s11172-010-0115-2
https://doi.org/10.1007/s11172-010-0115-2
Autor:
V. G. Granik, Lyudmila M. Alekseeva, Alexander S. Shashkov, S. Yu. Ryabova, N. S. Masterova, Vladimir V. Chernyshev
Publikováno v:
Russian Chemical Bulletin. 58:1973-1980
Reactions of 3-acetoxy-2-(2,2-dicyanovinyl)indole with hydrazine hydrate and methyl-and phenylhydrazines afforded new indolin-3-one derivatives, namely, 2-[(3,5-diaminopyrazol-4-yl)methylidene]indolin-3-ones. Reactions of the compounds obtained with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92dcbbeefac596cd56fbfa11d01bac7b
https://doi.org/10.1007/s11172-009-0269-y
https://doi.org/10.1007/s11172-009-0269-y
Publikováno v:
Russian Chemical Bulletin. 56:1588-1594
Derivatives of the new heterocyclic system 1,11-dihydro-4H-pyrimido[5′,4′: 5,6]pyrido[3,2-b]indol-4-one were synthesized by the reactions of 2-(2-cyanoprop-2-enylidene)indolin-3-ones, bearing the primary and secondary amino groups in position 3 o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f75931271543a96800410dcf9281a3bb
https://doi.org/10.1007/s11172-007-0248-0
https://doi.org/10.1007/s11172-007-0248-0
Autor:
L. M. Alekseeva, S. S. Kiselev, N. S. Masterova, S. Yu. Ryabova, M. I. Evstratova, Vladimir G Granik
Publikováno v:
ChemInform. 42
Acid treatment of β-(3-acetoxyindol-2-yl)-α-cyanoacrylic acid derivatives (ethyl ester and nitrile) with aqueous or gaseous HCl afforded novel 3-substituted 2-oxo-2,5-dihydropyra-no[3,2-b]indoles. 2-Oxo-2,5-dihydropyrano[3,2-b]indole-3-carbonitrile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::725021a8a2665061c2c23c8622b18853
https://doi.org/10.1002/chin.201111155
https://doi.org/10.1002/chin.201111155
Publikováno v:
ChemInform. 39
Derivatives of the new heterocyclic system 1,11-dihydro-4H-pyrimido[5′,4′: 5,6]pyrido[3,2-b]indol-4-one were synthesized by the reactions of 2-(2-cyanoprop-2-enylidene)indolin-3-ones, bearing the primary and secondary amino groups in position 3 o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1848c37f8019a6fd05d26c99426c74f
https://doi.org/10.1002/chin.200823153
https://doi.org/10.1002/chin.200823153
Autor:
S. S. Kiselev, M. I. Evstratova, Vladimir G Granik, S. Yu. Ryabova, N. S. Masterova, L. M. Alekseeva, E. A. Lisitsa
Publikováno v:
ChemInform. 38
Reactions of 2-(3,3-diamino-2-cyanoprop-2-enylidene)indolin-3-ones with amide acetals afforded derivatives of 3-aminomethyleneamino-2-cyano-9-oxo-9H-pyrrolo[1,2-a]indole and 3-amino-2-cyano-9-oxo-9H-pyrrolo[1,2-a]indole. The rate and pathway of the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72bb4c3e08e5fc7e30a656c70cb3a9af
https://doi.org/10.1002/chin.200745118
https://doi.org/10.1002/chin.200745118