Zobrazeno 1 - 10
of 19
pro vyhledávání: '"G. K. Bobyleva"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 17:352-357
The corresponding photochromic 5′,7′-disubstituted indolinospirochromenes were obtained by the reaction of 4,6-dialkoxy-5-nitrosalicylaldehydes, as well as 4,6-dimethyl-5-nitrosalicylaldehyde, with 1,3,3-trimethyl-2-methyleneindoline. Bulky elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::438f084f1e3f4ac847c0d0ba9fc569a9
https://doi.org/10.1007/bf00503335
https://doi.org/10.1007/bf00503335
Autor:
L. N. Lavrishcheva, E. M. Bondarenko, N. N. Suvorov, G. K. Bobyleva, N. M. Przhiyalgovskaya, I. V. Manakova, M. A. Gal'bershtam
Publikováno v:
Chemistry of Heterocyclic Compounds. 18:937-941
1,3,3-Trimethylspiro(indoline-2,2'-[2H]chromenes) with CH3 and CH3O groups in the 4–7 positions and NO2 and CH3O groups in the 6′ and 8′ positions were obtained by the reaction of 4,6-, 4,7-, 5,6-, and 6,7-dimethoxy- and 4-methyl-7-methoxy-2-me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2741ed9e9bfdf3879d0444449dcdfec7
https://doi.org/10.1007/bf00513436
https://doi.org/10.1007/bf00513436
Publikováno v:
Chemistry of Heterocyclic Compounds. 16:41-44
A number of photochromic indolinospirochromenes that contain an octadecyl substituent in the 1 position were synthesized. The introduction of an octadecyl group in place of a methyl group increases the stability of the merocyanine form in solution bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8d69d8276b726b060a7e3b063c14f8c
https://doi.org/10.1007/bf00475389
https://doi.org/10.1007/bf00475389
Autor:
N. M. Przhiyalgovskaya, M. A. Gal'bershtam, G. K. Bobyleva, N. N. Suvorov, I. B. Lazarenko, Yu. B. Pod'yachev
Publikováno v:
Chemistry of Heterocyclic Compounds. 20:1222-1225
Three photochromic indoline spirochromenes that contain styryl-substituents in the 5 position of the indoline part of the molecule were synthesized. The introduction of a styryl substituent into this position gives rise to a 15–20 nm bathochromic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ae4573967a87297e33f78766677a04f
https://doi.org/10.1007/bf00505711
https://doi.org/10.1007/bf00505711
Autor:
O. R. Khrolova, M. A. Gal'bershtam, G. K. Bobyleva, N. M. Przhiyalgovskaya, N. N. Suvorov, I. B. Lazarenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:1309-1313
A number of photochromic 1-carbethoxymethyl-3,3-dimethyl-6′-nitroindoline-2-spiro-2′-2H-chromenes were synthesized. The introduction of a carbethoxymethyl substituent at the nitrogen atom instead of a methyl group somewhat increases the rate of d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e675bb05a3f8e1a9e3d1a49c6b1a06c2
https://doi.org/10.1007/bf00469891
https://doi.org/10.1007/bf00469891
Publikováno v:
Chemistry of Heterocyclic Compounds. 18:1054-1057
A number of photochromic indoline spirochromenes with benzyl, acetonyl, and ethyl substituents attached to the nitrogen atom in the indoline part of the molecule were synthesized. The introduction of a benzyl group at the nitrogen atom in place of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a0f4c13fbb7b6e38c7ec7c424ff0ff6
https://doi.org/10.1007/bf00503194
https://doi.org/10.1007/bf00503194
Autor:
N. M. Przhiyalgovskaya, O. R. Khrolova, N. N. Suvorov, G. K. Bobyleva, M. A. Gal'bershtam, I. V. Manakova
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:859-861
6-Nitro-6′,7′-tetramethylene-substituted photochromic spirochromenes were synthesized from 5-aminotetralin. In the series of compounds thus obtained the electronic effect of the substituents in the 8 position on the dark decolorization reaction i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae98d96f557d548f195fafaac7b9fecd
https://doi.org/10.1007/bf00488910
https://doi.org/10.1007/bf00488910
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:1101-1103
The establishement of the principles that link the photochromic properties of indolinospirochromenes with the peculiarities of their structures may make it possible to purposefully select structures with practically valuable properties in this promis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13933cbc481347915be2913ef972bc8d
https://doi.org/10.1007/bf00471909
https://doi.org/10.1007/bf00471909
Autor:
I. V. Manakova, G. K. Bobyleva, M. A. Gal'bershtam, N. M. Przhiyalgovskaya, L. N. Kurkovskaya
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20b8ccf231e92bc42b3336e534b59117
https://doi.org/10.1002/chin.198831168
https://doi.org/10.1002/chin.198831168
Publikováno v:
Chemischer Informationsdienst. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de55508696e290ddfffba7a0dfbf4a58
https://doi.org/10.1002/chin.198139311
https://doi.org/10.1002/chin.198139311