Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Satenik G. Petrosyan"'
Autor:
Peter Langer, Tariel V. Ghochikyan, Lilit V. Khachatryan, Hayarpi M. Simonyan, Ashot S. Saghyan, Amanzhan T. Saginayev, Nazken K. Kelzhanova, Satenik G. Petrosyan, Arpine V. Geolchanyan, M. A. Samvelyan, Anna F. Mkrtchyan
Publikováno v:
Zeitschrift für Naturforschung B. 69:451-460
An efficient method for the asymmetric synthesis of a-amino acids, containing furyl- and thiophenyl-substituted triazoles in their side-chain, is reported. The strategy relies on Michael addition of 3,4,5-substituted 1,2,4-triazoles to the C=C bond o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f6afb9eb12de4866e37c543deea5b2b
https://doi.org/10.5560/znb.2014-3221
https://doi.org/10.5560/znb.2014-3221
Autor:
Satenik Mkrtchyan, Ashot S. Saghyan, Gnel M. Mkrtchyan, Anna F. Mkrtchyan, Satenik G. Petrosyan, Hayarpi M. Simonyan, Ashot Gevorgyan, Peter Langer, Ani S. Dadayan, Arpine V. Geolchanyan, Viktor O. Iaroshenko
Publikováno v:
Tetrahedron: Asymmetry. 24:229-232
The conjugate addition of S-, N- and O-heterocyclic nucleophiles to the C C bond of dehydroalanine, bonded as a Schiff’s base to the chiral auxiliary (S)-2-[N-(N′-benzylprolyl)amino]benzophenone in the coordination sphere of NiII, resulted in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d14d264ad399ad96418d52847439fff0
https://doi.org/10.1016/j.tetasy.2013.01.014
https://doi.org/10.1016/j.tetasy.2013.01.014
Autor:
Henry A. Panosyan, Arpine V. Geolchanyan, Victor N. Khrustalev, Slavik A. Dadayan, A. S. Saghiyan, L. L. Manasyan, Victor I. Maleev, Satenik G. Petrosyan
Publikováno v:
Synthetic Communications. 41:493-506
The reactions of asymmetric C-alkylation of glycine and alanine in NiII complexes of their Schiff's bases with modified chiral auxiliaries (S)-2-N-[(N′-2-chlorobenzylprolyl)amino]benzophenone and (S)-2-N-[N′-(3,4-dimethylbenzylprolyl)amino]benzop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7851f3e515043fa23f8d94c1725d4c04
https://doi.org/10.1080/00397911003587531
https://doi.org/10.1080/00397911003587531
Autor:
L. L. Manasyan, A. A. Petrosyan, Satenik G. Petrosyan, V. I. Maleev, Viktor N. Khrustalev, A. S. Saghiyan, Slavik A. Dadayan
Publikováno v:
Russian Chemical Bulletin. 55:442-450
NiII complexes with the Schiff bases of (E)-and (Z)-2-aminobut-2-enoic acids were obtained with (S)-N-(2-benzoylphenyl)-1-(2-chlorobenzyl)pyrrolidine-2-carboxamide and (S)-N-(2-benzoylphenyl)-1-(3,4-dimethylbenzyl)pyrrolidine-2-carboxamide as new chi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::342b3a09f448bed826a3c7059dc1ece2
https://doi.org/10.1007/s11172-006-0276-1
https://doi.org/10.1007/s11172-006-0276-1
Autor:
A. S. Saghiyan, Victor N. Khrustalev, Arpine V. Geolchanyan, Satenik G. Petrosyan, Luisa L. Manasyan, Silva M. Djamgaryan, Victor I. Maleev, Sargis A. Andreasyan, Slavik A. Dadayan
Publikováno v:
Tetrahedron: Asymmetry. 17:455-467
New modified chiral auxiliaries (S)-N-(2-benzoylphenyl)-1-(2-chlorobenzyl)pyrrolidine-2-carboxamide (2-CBPB) and (S)-N-(2-benzoylphenyl)-1-(3,4-dimethylbenzyl)pyrrolidine-2-carboxamide (3,4-DMBPB) and their NiII complexes of Schiff’s base with glyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b0a11b93747e31042fffbd1b254e99f
https://doi.org/10.1016/j.tetasy.2006.01.026
https://doi.org/10.1016/j.tetasy.2006.01.026
Autor:
V.S. Haroutunyan, Yu. N. Belokon, Satenik G. Petrosyan, A. S. Saghiyan, K. Fisher, Tariel V. Ghochikyan, Arpine V. Geolchanyan, A. A. Avetisyan
Publikováno v:
Tetrahedron: Asymmetry. 15:705-711
A new efficient method of asymmetric synthesis of β-heterocycle substituted l -α-amino acids through the addition of 3-amino-1,2,4-thiodiazole and 5-mercapto-1,2,4-triazoles, containing various substituents at the 3 and 4 positions, to the CC bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4842d05a4259bf0dbf71ebfb57d2eaf1
https://doi.org/10.1016/j.tetasy.2003.12.007
https://doi.org/10.1016/j.tetasy.2003.12.007
Autor:
Arpine V. Geolchanyan, Satenik G. Petrosyan, Hayarpi M. Simonyan, Giovanni N. Roviello, Ashot S. Saghyan, Valentina Roviello, Domenica Musumeci
Publikováno v:
Amino acids (Wien, Print) 46 (2014): 2325–2332. doi:10.1007/s00726-014-1782-3
info:cnr-pdr/source/autori:Saghyan, Ashot S.; Simonyan, Hayarpi M.; Petrosyan, Satenik G.; Geolchanyan, Arpine V.; Roviello, Giovanni N.; Musumeci, Domenica; Roviello, Valentina/titolo:Thiophenyl-substituted triazolyl-thione L-alanine: asymmetric synthesis, aggregation and biological properties/doi:10.1007%2Fs00726-014-1782-3/rivista:Amino acids (Wien, Print)/anno:2014/pagina_da:2325/pagina_a:2332/intervallo_pagine:2325–2332/volume:46
info:cnr-pdr/source/autori:Saghyan, Ashot S.; Simonyan, Hayarpi M.; Petrosyan, Satenik G.; Geolchanyan, Arpine V.; Roviello, Giovanni N.; Musumeci, Domenica; Roviello, Valentina/titolo:Thiophenyl-substituted triazolyl-thione L-alanine: asymmetric synthesis, aggregation and biological properties/doi:10.1007%2Fs00726-014-1782-3/rivista:Amino acids (Wien, Print)/anno:2014/pagina_da:2325/pagina_a:2332/intervallo_pagine:2325–2332/volume:46
In this work, we report the asymmetric synthesis and characterization of an artificial amino acid based on triazolyl-thione l-alanine, which was modified with a thiophenyl-substituted moiety, as well as in vitro studies of its nucleic acid-binding ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::906a9b8911a4a58b44d53c04f377aef3
http://hdl.handle.net/11588/586698
http://hdl.handle.net/11588/586698
Autor:
Satenik G. Petrosyan, Slavik A. Dadayan, A. S. Saghiyan, L. L. Manasyan, Henry A. Panosyan, Victor N. Khrustalev, Victor I. Maleev, Arpine V. Geolchanyan
Publikováno v:
ChemInform. 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff8baa560888865da03723a69c105d86
https://doi.org/10.1002/chin.201132187
https://doi.org/10.1002/chin.201132187