Zobrazeno 1 - 5
of 5
pro vyhledávání: '"D. A. Partsvaniya"'
Autor:
R. N. Akhvlediani, N. N. Suvorov, L. N. Kuleshova, E. N. Gnrdeev, D. A. Partsvaniya, V. E. Zhigachev
Publikováno v:
Chemistry of Heterocyclic Compounds. 22:1311-1315
Reaction of 3,4-ethylenedioxyphenyldiazonium chloride with ethyl 2-methylacetoacetate and subsequent cyclization of the 3,4-ethylenedioxyphenylhydrazone of ethyl pyruvate gives a 1∶4 mixture of 4,5- and 5,6-ethylenedioxy-2-ethoxycarbonylindoles, re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14da3453ad46790ef8ff9b6593017900
https://doi.org/10.1007/bf00474350
https://doi.org/10.1007/bf00474350
Autor:
M. M. Vigdorchik, L. N. Kuleshova, D. A. Partsvaniya, M. D. Mashkovskii, N. N. Suvorov, T. K. Trubitsyna, R. N. Akhvlediani, E. N. Gordeev
Publikováno v:
Pharmaceutical Chemistry Journal. 20:833-838
It should be noted that with the Japp--Klingemann reaction hydrazone II is obtained in the syn form, which was confirmed by PMR data in CDCI~ (chemical shift of 7 NH is 12.73 ppm). The syn form of hydrazone II is easily converted to the anti form by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8341ab6cf94b46a882a23a5a1a1dde3e
https://doi.org/10.1007/bf00763713
https://doi.org/10.1007/bf00763713
Autor:
L. N. Kuleshova, V. E. Zhigachev, D. A. Partsvaniya, N. N. Suvorov, E. N. Gordeev, R. N. Akhvlediani
Publikováno v:
Chemistry of Heterocyclic Compounds. 23:755-757
The reactivity of 4,5-ethylenedioxyindole in the Vilsmeier and Mannich reactions and in diazo coupling was studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f86e458fdc3778eb5b3a719ca69d91c7
https://doi.org/10.1007/bf00475642
https://doi.org/10.1007/bf00475642
ChemInform Abstract: Synthesis and Pharmacological Activity of 5,6- and 4,5-Ethylenedioxytryptamines
Autor:
D. A. Partsvaniya, N. N. Suvorov, E. N. Gordeev, M. M. Vigdorchik, L. N. Kuleshova, T. K. Trubitsyna, R. N. Akhvlediani, M. D. Mashkovskii
Publikováno v:
ChemInform. 18
It should be noted that with the Japp--Klingemann reaction hydrazone II is obtained in the syn form, which was confirmed by PMR data in CDCI~ (chemical shift of 7 NH is 12.73 ppm). The syn form of hydrazone II is easily converted to the anti form by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9babd57202972c47f526ec4aa3876c9c
https://doi.org/10.1002/chin.198730202
https://doi.org/10.1002/chin.198730202
Autor:
N. N. Suvorov, R. N. Akhvlediani, D. A. Partsvaniya, E. N. Gordeev, L. N. Kuleshova, V. E. Zhigachev
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83d71298498698cba6b67e4651c19a8a
https://doi.org/10.1002/chin.198807206
https://doi.org/10.1002/chin.198807206