Zobrazeno 1 - 10
of 75
pro vyhledávání: '"N. M. Przhiyalgovskaya"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 45:501-523
The review contains data on methods for the production of ethynylindoles and their derivatives. The whole range of transformations of these compounds is examined in detail. It is demonstrated that indoles containing highly unsaturated groups are inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb7bf4f94511c0377d257d254a39618a
https://doi.org/10.1007/s10593-009-0304-9
https://doi.org/10.1007/s10593-009-0304-9
Autor:
S. M. Aldoshin, O. S. Filipenko, Yu. M. Chunaev, L. N. Kurkovskaya, N. A. Martem'yanova, N. M. Przhiyalgovskaya
Publikováno v:
Chemistry of Heterocyclic Compounds. 29:356-361
Salicylaldehyde, 5-chlorosalicylaldehyde, or o-vanillin will react with 2-imino-3,5-dimethylthiazolidine to form previously unknown bis(3,5-dimethylthiazolidin-2-ylideneamino)-2-hydroxyphenylmethanes. If strong electron-acceptor groups are present on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b76ba44eeebcf54eece644c324aadfdb
https://doi.org/10.1007/bf00531517
https://doi.org/10.1007/bf00531517
Autor:
S. M. Aldoshin, Yu. M. Chunaev, N. M. Przhiyalgovskaya, O. S. Filipenko, N. A. Martem'yanova, L. N. Kurkovskaya
Publikováno v:
Chemistry of Heterocyclic Compounds. 29:352-355
As indicated by PMR spectroscopic data, 2-amino-5-methylthiazoline and 2-methylamino-5-methylthiazoline exist in the imine form in the temperature interval from +20° to −100° C. Interaction of the 2-amino-5-methylthiazoline with methyl iodide res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d43ac013e37077c6719dbeb20385443c
https://doi.org/10.1007/bf00531516
https://doi.org/10.1007/bf00531516
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9114e42dc343793af8c2360cdbdd4ba
https://doi.org/10.1002/chin.199309214
https://doi.org/10.1002/chin.199309214
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::156a10d9b7269875fcafb94c77153e6e
https://doi.org/10.1002/chin.199349167
https://doi.org/10.1002/chin.199349167
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac2914ed107ebf11625f4954c9402de7
https://doi.org/10.1002/chin.199322318
https://doi.org/10.1002/chin.199322318
Autor:
O. S. Filipenko, N. M. Przhiyalgovskaya, Yu. M. Chunaev, S. M. Aldoshin, L. N. Kurkovskaya, N. A. Martem'yanova
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26bfb369becb7b862d7263a1c30089f6
https://doi.org/10.1002/chin.199405164
https://doi.org/10.1002/chin.199405164
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:618-625
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd4a5569af23ae44f152ddda193a4255
https://doi.org/10.1007/bf00529332
https://doi.org/10.1007/bf00529332
Publikováno v:
ChemInform. 40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3af4a0518fbb57c756d8c7b0abbbffd2
https://doi.org/10.1002/chin.200952245
https://doi.org/10.1002/chin.200952245
Autor:
Anatoly V. Metelitsa, I. Yu. Grishin, Yu. M. Chunaev, M. I. Knyazhanskii, N. M. Przhiyalgovskaya, N. V. Volbushko
Publikováno v:
Chemistry of Heterocyclic Compounds. 27:1012-1015
Only E ⇄ Z isomerization is observed for the steady irradiation of fulgides based on 1,2-dimethyl-3-formylindole in contrast to the analogs based on 3-acetylindole. The formation of cyclic photoisomers is registered by the method of impulse photoly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d88f9981515106f06a0734868e83cf91
https://doi.org/10.1007/bf00484368
https://doi.org/10.1007/bf00484368