Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Arpine V. Geolchanyan"'
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:
Ashot S. Saghyan, L. L. Manasyan, Peter Langer, Hayarpi M. Simonyan, Nelli Hovhannisyan, Lala A. Stepanyan, Tariel V. Ghochikyan, Viktor O. Iaroshenko, Samvel G. Ghazaryan, Arpine V. Geolchanyan, Ashot Gevorgyan, Vahe T. Ghochikyan
Publikováno v:
Tetrahedron: Asymmetry. 23:891-897
The asymmetric synthesis of novel non-proteinogenic β-heterocyclic α-amino acids via the diastereoselective conjugate addition of heterocyclic nucleophiles to the dehydroalanine moiety of chiral Ni(II) complexes has been studied. The complexes were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::662213638318b7ab79fbd280613c693e
https://doi.org/10.1016/j.tetasy.2012.05.022
https://doi.org/10.1016/j.tetasy.2012.05.022
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:
Slavik Arshak Dadayan, Victor I. Maleev, Hrant R. Ajvazyan, Ani Slavik Dadayan, Anna F. Mkrtchyan, Ashot S. Saghyan, Hasmik H. Hambardzumyan, Arpine V. Geolchanyan, Victor N. Khrustalev, Luiza L. Manasyan
Publikováno v:
Tetrahedron: Asymmetry. 21:2956-2965
New fluorine-containing chiral auxiliaries ( S )- N -(2-benzoylphenyl)-1-(2-fluorobenzyl)-, ( S )- N -(2-benzoylphenyl)-1-(3-fluorobenzyl)-, and ( S )- N -(2-benzoylphenyl)-1-(4-fluorobenzyl)-pyrrolidine-2-carboxamide and their Ni II complexes of Sch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6887892ce163386a74f0663132bdc50
https://doi.org/10.1016/j.tetasy.2010.11.024
https://doi.org/10.1016/j.tetasy.2010.11.024
Autor:
Luiza L. Manasyan, V. I. Maleev, Arpine V. Geolchanyan, Henry A. Panosyan, Tatiana F. Savel'eva, Lala A. Stepanyan, Hrant R. Ajvazyan, Ashot S. Saghiyan, Silva M. Djamgaryan
Publikováno v:
Tetrahedron: Asymmetry. 21:2638-2645
New chiral NiII complexes of Schiff bases of dehydroalanine with modified chiral auxiliaries (S)-2-N-[N′-(3,4-dichlorobenzyl)prolyl]aminobenzophenone (3,4-DCBPB), (S)-2-N-[N′-(3,4-dimethylbenzyl)prolyl]aminobenzophenone (3,4-DMBPB), (S)-2-N-[N′
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29b975fc4679814eb952055be040fde3
https://doi.org/10.1016/j.tetasy.2010.10.015
https://doi.org/10.1016/j.tetasy.2010.10.015
Autor:
A. S. Saghiyan, Arpine V. Geolchanyan
Publikováno v:
Synthetic Communications. 36:3667-3677
A new method for asymmetric synthesis of all possible stereomers of 4‐aminoglutamic acid has been developed. The method is based on asymmetric Michael condensation of the nucleophilic moiety of glycine and electrophilic moiety of dehydroalanine in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::024f295757d5c624fb2fd0dee88f0f3b
https://doi.org/10.1080/00397910600945951
https://doi.org/10.1080/00397910600945951
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:
T. V. Kochickyan, L. L. Manasyan, Slavik A. Dadayan, Yu. N. Belokon, Vitali I. Tararov, V. S. Harutyunyan, A. S. Saghiyan, N. R. Martirosyan, Arpine V. Geolchanyan, G. M. Mkrtchyan, V. I. Maleev, A. A. Avetisyan
Publikováno v:
Russian Chemical Bulletin. 53:932-935
An efficient method was developed for the asymmetric synthesis of (R)-S-(1,2,4-triazol-3-yl)cysteines by the addition of 3,4-disubstituted 1,2,4-triazole-5-thiols at the electrophilic C=C bond in a NiII complex of a Schiff base of dehydroalanine with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77a4c5ad68c12ff2c3682953b4fc6a50
https://doi.org/10.1023/b:rucb.0000037866.13065.c7
https://doi.org/10.1023/b:rucb.0000037866.13065.c7
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