Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alexander N, Koronatov"'
Autor:
Julia O. Strelnikova, Mikhail S. Novikov, Nikolai V. Rostovskii, Alexander N. Koronatov, Alexander F. Khlebnikov, Mariya A. Kryukova, Olesya V. Khoroshilova
Publikováno v:
Organic Letters. 23:4173-4178
1,4,8-Triazaocta-1,3,5,7-tetraenes, generated in situ by Rh2(Piv)4-catalyzed denitrogenative coupling of pyrazoles with 1-sulfonyl-1,2,3-triazoles, smoothly form 2,6,8-triazabicyclo[3.2.1]octa-3,6-dienes via intramolecular aza-Diels-Alder cycloadditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faa4c68aaebff319c3db713476d99c53
https://doi.org/10.1021/acs.orglett.1c01092
https://doi.org/10.1021/acs.orglett.1c01092
Autor:
Dmitrii S. Vasilchenko, Anastasiya V. Agafonova, Ivan V. Simdianov, Alexander N. Koronatov, Pavel A. Sakharov, Ilya A. Romanenko, Nikolai V. Rostovskii, Alexander F. Khlebnikov, Mikhail S. Novikov
Publikováno v:
Tetrahedron Letters. :154580
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7f75d6cf6eacb3709b9dab863bcbb3a
https://doi.org/10.1016/j.tetlet.2023.154580
https://doi.org/10.1016/j.tetlet.2023.154580
Autor:
Kseniia K. Afanaseva, Pavel A. Sakharov, Alexander N. Koronatov, Mikhail S. Novikov, Nikolai V. Rostovskii, Alexander F. Khlebnikov
Publikováno v:
Organic Chemistry Frontiers. 8:1474-1481
A method for the synthesis of 1-alkyl-3-sulfonamido-1H-pyrroles by the Rh(II)-catalyzed denitrogenative coupling of two different types of 1,2,3-triazoles, 1-alkyl-4-aryl- and 1-sulfonyl-4-aryl-1,2,3-triazoles, has been developed. According to the DF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::249d796634f717ef2708459a882800ff
https://doi.org/10.1039/d0qo01571g
https://doi.org/10.1039/d0qo01571g
Publikováno v:
Organic Letters. 22:7958-7963
A method for the synthesis of densely substituted 4-pyrrolin-2-ones by Rh(II)-catalyzed denitrogenative transannulation of 1-alkyl-4-aryl-1H-1,2,3-triazoles with diazo esters has been developed. The reaction proceeds via an attack of the rhodium-boun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0abd6e781710149294e80ab432b2f1ef
https://doi.org/10.1021/acs.orglett.0c02893
https://doi.org/10.1021/acs.orglett.0c02893
Autor:
Alexander N. Koronatov, Alexander F. Khlebnikov, Ilia A. Smetanin, Vasilii V. Potapenkov, Anastasiya V. Agafonova, Mikhail S. Novikov, Nikolai V. Rostovskii
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:881-887
1-Acyl-2-azabuta-1,3-dienes underwent rearrangement to 4-pyrrolin-2-ones in the presence of acidic catalysts (silica gel or ZnCl2) and water. The reaction proceeded via the formation of 2,3-dihydroxy-3,4-dihydropyrrole and 2-hydroxy-2Н-pyrrole inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acc742b6df3d9d5e22f3834b48d57677
https://doi.org/10.1007/s10593-020-02745-x
https://doi.org/10.1007/s10593-020-02745-x
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:1185-1189
A one-pot method for the synthesis of 3-(pyridin-2-yl)-2,3-dihydroazetes was developed on the basis of Rh2(esp)2-catalyzed reaction of diazoesters with 3-aryl-2-(pyridin-2-yl)-2H-azirines. To prevent deactivation of the catalyst with the pyridine-con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3d579679511654485a8e5d048859de0
https://doi.org/10.1007/s10593-019-02599-y
https://doi.org/10.1007/s10593-019-02599-y
Autor:
Alexander N. Koronatov, Pavel A. Sakharov, Vladimir V. Sharoyko, Elizaveta V. Rogacheva, Alexander F. Khlebnikov, Mikhail S. Novikov, Nikolai V. Rostovskii, Tatiana B. Tennikova, Liudmila Kraeva, Artem G. Glukharev
Publikováno v:
RSC Advances. 9:37901-37905
Non-natural 2H-azirine-2-carboxylic acids were obtained in high yields by FeCl2-catalyzed isomerization of 5-chloroisoxazoles to azirine-2-carbonyl chlorides followed by their hydrolysis. The 3-aryl- and 3-heteroaryl-substituted acids are stable duri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f024b7db14c7c1382529ad23bab13578
https://doi.org/10.1039/c9ra09345a
https://doi.org/10.1039/c9ra09345a
Autor:
Alexander F. Khlebnikov, Anastasiya V. Agafonova, Alexander N. Koronatov, Pavel A. Sakharov, Mikhail S. Novikov, Nikolai V. Rostovskii, Liudmila Kraeva, Elizaveta V. Rogacheva
Publikováno v:
Organicbiomolecular chemistry. 18(46)
Azirine-containing dipeptides and depsipeptides with a wide range of substituents have been synthesized in high yields via the Passerini and Ugi multicomponent reactions (MCRs) using 2H-azirine-2-carboxylic acids as the acid component. The obtained M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a03e67a949f1c678cbba4e4bd07e6b8
https://pubmed.ncbi.nlm.nih.gov/33170920
https://pubmed.ncbi.nlm.nih.gov/33170920
Publikováno v:
Organic letters. 22(20)
A method for the synthesis of densely substituted 4-pyrrolin-2-ones by Rh(II)-catalyzed denitrogenative transannulation of 1-alkyl-4-aryl-1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::116005cf6e872c2151ed8781a7c787d6
https://pubmed.ncbi.nlm.nih.gov/33026817
https://pubmed.ncbi.nlm.nih.gov/33026817
Autor:
Pavel A, Sakharov, Alexander N, Koronatov, Alexander F, Khlebnikov, Mikhail S, Novikov, Artem G, Glukharev, Elizaveta V, Rogacheva, Liudmila A, Kraeva, Vladimir V, Sharoyko, Tatiana B, Tennikova, Nikolai V, Rostovskii
Publikováno v:
RSC advances. 9(65)
Non-natural 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b6f6a007fdaaefbd9a8f3370783b8c10
https://pubmed.ncbi.nlm.nih.gov/35541773
https://pubmed.ncbi.nlm.nih.gov/35541773