Zobrazeno 1 - 9
of 9
pro vyhledávání: '"D. A. Avakimyan"'
Autor:
A. I. Markosyan, G. M. Stepanyan, K. K. Airapetyan, S. A. Gabrielyan, S. S. Mamyan, D. A. Avakimyan, V. Z. Shirinyan, A. V. Zakharov, F. G. Arsenyan
Publikováno v:
Pharmaceutical Chemistry Journal. 53:15-22
A method for the synthesis of 1-amino-3,3-dimethyl-3,4-dihydronaphthaline-2-carbonitrile (β-aminonitrile) was developed and used to synthesize Schiff bases, thioureide and chloracetamide derivatives. This latter was cyclized to 5,5-dimethyl-2-chloro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38f9b8c0966b26997a61bdd202908108
https://doi.org/10.1007/s11094-019-01948-7
https://doi.org/10.1007/s11094-019-01948-7
Autor:
O. A. Papoyan, N. K. Gasparyan, A. A. Tatevosyan, G. A. Gevorgyan, H. A. Panosyan, D. A. Avakimyan
Publikováno v:
Pharmaceutical Chemistry Journal. 51:107-110
New α-bromoethanones were synthesized by bromination of 1-[4(3,4)-substituted phenyl]-2-phenyl[3(4)-substituted phenyl]ethanones and were reacted with various amines in Et2O to produce the corresponding 1-[4-alkoxyphenyl(3-bromophenyl)]-2-phenyl-[3(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d47fb6599c54e9fb19f80f7145ca0b56
https://doi.org/10.1007/s11094-017-1565-8
https://doi.org/10.1007/s11094-017-1565-8
Publikováno v:
Russian Journal of Organic Chemistry. 52:1308-1311
Methods have been developed for the synthesis of new heterocyclic systems, spiro[chromene-4,3′- indoles] and spiro[indole-3,4′-quinolines] by the base-catalyzed domino reaction of isatins with 5,5-dimethylcyclohexane- 1,3-dione (or 5,5-dimethyl-3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9db18e8ea6830bbeff9185b933178e0f
https://doi.org/10.1134/s1070428016090098
https://doi.org/10.1134/s1070428016090098
Autor:
N. K. Gasparyan, D. A. Avakimyan, O. A. Papoyan, G. A. Gevorgyan, A. A. Tatevosyan, G. A. Panosyan, R. G. Paronikyan
Publikováno v:
Pharmaceutical Chemistry Journal. 45:461-465
New 2-(4-chlorophenyl)-3-morpholin-4-yl-1-(4-alkoxyphenyl)propan-1-ones were synthesized via aminomethylation of 2-(4-chlorophenyl)-1-(4-alkoxyphenyl)ethanones. Reduction of the former by lithium aluminum hydride produced 2-(4-chlorophenyl)-3-morphol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::783322068bb7f023b0b74b5925386151
https://doi.org/10.1007/s11094-011-0655-2
https://doi.org/10.1007/s11094-011-0655-2
Publikováno v:
Pharmaceutical Chemistry Journal. 45:26-29
A series of 2-hydrazino-5-bromomethyl-4,5-dihydrothiazole hydrazones based on substituted N4-allylthiosemicarbazones was synthesized. Some of these hydrazones were found to have moderate antibacterial activity against Staphylococcus aureus 209P, 1 an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae9dfea057bdd2c8b0b18fe95614bfe3
https://doi.org/10.1007/s11094-011-0554-6
https://doi.org/10.1007/s11094-011-0554-6
Autor:
M. N. Malakyan, S. A. Badzhinyan, D. É. Egiazaryan, D. A. Avakimyan, G. A. Panosyan, N. K. Gasparyan, G. A. Gevorgyan, L. A. Vardevanyan
Publikováno v:
Pharmaceutical Chemistry Journal. 45
Interaction of α-phenyl-β-piperidino-4-substituted propiophenones with Grignard reagents in ether was used to synthesize 1-(4-substituted phenyl)-1-alkyl(aryl)-2-phenyl-3-piperidinopropan-1-ols. The antibacterial and antioxidant properties of the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ed186757cf3902ecd7baa6971147841
https://doi.org/10.1007/s11094-011-0600-4
https://doi.org/10.1007/s11094-011-0600-4
Publikováno v:
Pharmaceutical Chemistry Journal. 27:759-762
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::267ce47bc31f793c23ede6a6dbf0f4f6
https://doi.org/10.1007/bf00780403
https://doi.org/10.1007/bf00780403
Autor:
E. G. Paronikyan, S. A. Vartanyan, D. A. Avakimyan, L. G. Akopyan, G. M. Paronikyan, T. R. Akopyan
Publikováno v:
Pharmaceutical Chemistry Journal. 15:482-486
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05cdf45c558ed48fc1bc036325feaf4d
https://doi.org/10.1007/bf00758532
https://doi.org/10.1007/bf00758532
Autor:
L. G. Akopyan, T. R. Akopyan, E. G. Paronikyan, S. A. Vartanyan, G. M. Paronikyan, D. A. Avakimyan
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::777d4068710d282eac4f0a13d63c2e96
https://doi.org/10.1002/chin.198202247
https://doi.org/10.1002/chin.198202247