Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Evgenii S. Gorlov"'
Autor:
Evgenii S. Gorlov, Diana V. Shuingalieva, Alexey I. Ilovaisky, Vera A. Vil’, Alexander O. Terent’ev
Publikováno v:
Molbank, Vol 2023, Iss 2, p M1651 (2023)
Here, we first report the 2′-acyloxy-1,3-dicarbonyl compound construction in a three-component oxidative reaction of alkyl ketene dimer with cyclic diacyl peroxide and trimethyl orthoformate. The discovered synthesis allows us to form 2′-function
Externí odkaz:
https://doaj.org/article/05b421b15ad04ec09177b675c78473f1
Publikováno v:
Molbank, Vol 2022, Iss 4, p M1497 (2022)
Over the past decades, studies of cyclic diacyl peroxides have shown superior or even fundamentally new reactivity compared to their acyclic counterparts in various reactions. Previously, the scope of cyclic diacyl peroxides was limited to the mono p
Externí odkaz:
https://doaj.org/article/04f908b62c514d69a7bfa76600d73be3
Autor:
Vera A. Vil’, Evgenii S. Gorlov, Diana V. Shuingalieva, Artem Yu. Kunitsyn, Nikolai V. Krivoshchapov, Michael G. Medvedev, Igor V. Alabugin, Alexander O. Terent’ev
Publikováno v:
The Journal of Organic Chemistry. 87:13980-13989
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4669da2d9a969f1e6177d837db665d12
https://doi.org/10.1021/acs.joc.2c01634
https://doi.org/10.1021/acs.joc.2c01634
Publikováno v:
Organic Chemistry Frontiers. 8:3091-3101
An acetal fragment is a well-known protective group which does not activate the neighboring α-position. Selective functionalization of the non-activated acetal α-position with formal retaining of the acetal fragment was realized using cyclic diacyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60941a86b2ab6994498596368ec1c7d8
https://doi.org/10.1039/d1qo00494h
https://doi.org/10.1039/d1qo00494h
Autor:
Oleg V. Bityukov, Valentina M. Merkulova, Vera A. Vil, Evgenii S. Gorlov, Yulia E. Romanova, Yana A. Barsegyan, Alexander O. Terent'ev
Publikováno v:
Advanced Synthesis & Catalysis. 361:3173-3181
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::396c4cf4756c0867e404c090a238b3e5
https://doi.org/10.1002/adsc.201900271
https://doi.org/10.1002/adsc.201900271
Autor:
Oleg V. Bityukov, Evgenii S. Gorlov, Alexander O. Terent'ev, Gennady I. Nikishin, Kasimir K. Pivnitsky, Igor B. Krylov, Vera A. Vil
Publikováno v:
Mendeleev Communications. 29:132-134
Malonyl peroxides were used for the one-pot construction of hybrid structures by conjugation of heterocycle (3H-pyrazol-3-one, isoxazol-5(2H)-one, pyrazolidine-3,5-dione, or barbituric acid) and amine or alcohol. The first stage represents oxidative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90560f8307dd37e148e096f8e2909756
https://doi.org/10.1016/j.mencom.2019.03.003
https://doi.org/10.1016/j.mencom.2019.03.003
Autor:
Olga N. Rusina, Evgenii S. Gorlov, Alexander A. Korlyukov, Gennady I. Nikishin, Alexander O. Terent'ev, Waldemar Adam, Vera A. Vil
Publikováno v:
ChemistrySelect. 2:3334-3341
Oxidative functionalization of 3H-pyrazol-3-ones, isoxazol-5(2H)-ones, pyrazolidine-3,5-diones, and barbituric acids by malonyl peroxides results exclusively in C−O coupling products. Traditional hydroxylation, formation of carbonyl groups, or oxid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77ff4675ed357c35eed7de54ae818f9a
https://doi.org/10.1002/slct.201700720
https://doi.org/10.1002/slct.201700720
Autor:
Evgenii S. Gorlov, Alexander O. Terent'ev, Vera A. Vil, Kasimir K. Pivnitsky, Gennady I. Nikishin, Waldemar Adam
Publikováno v:
ChemInform. 47
The lanthanide-catalyzed oxidative C-O coupling of 1,3-dicarbonyl compounds with diacyl peroxides, specifically the cyclic malonyl peroxides, has been developed. An important feature of this new reaction concerns the advantageous role of the peroxide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a39cd99c5651b42893a9ad38769bca9
https://doi.org/10.1002/chin.201626081
https://doi.org/10.1002/chin.201626081
Autor:
Alexander O. Terent'ev, Vera A. Vil, Evgenii S. Gorlov, Kasimir K. Pivnitsky, Gennady I. Nikishin, Waldemar Adam
Publikováno v:
The Journal of organic chemistry. 81(3)
The lanthanide-catalyzed oxidative C-O coupling of 1,3-dicarbonyl compounds with diacyl peroxides, specifically the cyclic malonyl peroxides, has been developed. An important feature of this new reaction concerns the advantageous role of the peroxide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21c7214f9db163f3eb1bc6a0807b152d
https://pubmed.ncbi.nlm.nih.gov/26745010
https://pubmed.ncbi.nlm.nih.gov/26745010