Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ekaterina A. Lystsova"'
Publikováno v:
Molbank, Vol 2023, Iss 4, p M1749 (2023)
The reaction of 3-benzoylpyrrolo[2,1-c][1,4]benzothiazine-1,2,4-trione with 2,3-dimethylquinoxaline afforded 3-benzoyl-2-hydroxy-3a-[(3-methylquinoxalin-2-yl)methyl]-1H-pyrrolo[2,1-c][1,4]benzothiazine-1,4(3aH)-dione in a moderate yield. The compound
Externí odkaz:
https://doaj.org/article/de1837baa0274a6088fc1736044217c1
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 646-657 (2023)
Pyrrolo[2,1-b][1,3]benzothiazoles are an important class of fused sulfur and nitrogen-containing heterocycles intensively studied in medicinal chemistry and pharmacology. In the present paper, a new synthetic approach to pyrrolobenzothiazoles is deve
Externí odkaz:
https://doaj.org/article/74265c0683424377be20ea0bd8eb0f28
Autor:
Ekaterina A. Lystsova, Anastasia D. Novokshonova, Pavel V. Khramtsov, Alexander S. Novikov, Maksim V. Dmitriev, Andrey N. Maslivets, Ekaterina E. Khramtsova
Publikováno v:
Molecules, Vol 29, Iss 9, p 2089 (2024)
1H-Pyrrole-2,3-diones, fused at [e]-side with a heterocycle, are suitable platforms for the synthesis of various angular polycyclic alkaloid-like spiroheterocycles. Recently discovered sulfur-containing [e]-fused 1H-pyrrole-2,3-diones (aroylpyrrolobe
Externí odkaz:
https://doaj.org/article/5dfac939419f4fe0a71b6b0fd70fa14d
Autor:
Ekaterina A. Lystsova, Alexander S. Novikov, Maksim V. Dmitriev, Andrey N. Maslivets, Ekaterina E. Khramtsova
Publikováno v:
Molecules, Vol 28, Iss 14, p 5495 (2023)
Acyl(imidoyl)ketenes are highly reactive heterocumulenes that enable diversity-oriented synthesis of various drug-like heterocycles. Such ketenes, bearing heterocyclic substituents, afford angularly fused pyridin-2(1H)-ones in their [4+2]-cyclodimeri
Externí odkaz:
https://doaj.org/article/0b61e3dac1a64b94883ac21da3eadff8
Autor:
Ekaterina E. Khramtsova, Ekaterina A. Lystsova, Evgeniya V. Khokhlova, Maksim V. Dmitriev, Andrey N. Maslivets
Publikováno v:
Molecules, Vol 26, Iss 23, p 7179 (2021)
The 3-hydroxy-1,5-dihydro-2H-pyrrol-2-one motif is a valuable scaffold in drug discovery. The replacement of the 3-oxy fragment in 3-hydroxy-1,5-dihydro-2H-pyrrol-2-ones-based compounds with a 3-amino one (3-amino analogs of 3-hydroxy-1,5-dihydro-2H-
Externí odkaz:
https://doaj.org/article/6cced38f3f07426289b38ef6b4e0b0ab
Publikováno v:
Symmetry, Vol 13, Iss 8, p 1509 (2021)
Polyfunctional building blocks are essential for the implementation of diversity-oriented synthetic strategies, highly demanded in small molecule libraries’ design for modern drug discovery. Acyl(imidoyl)ketenes are highly reactive organic compound
Externí odkaz:
https://doaj.org/article/448f4b57f6d841ce8cde34c215b72584
Autor:
Ekaterina E. Khramtsova, Ekaterina A. Lystsova, Maksim V. Dmitriev, Radomir Jasiński, Andrey N. Maslivets
Publikováno v:
ChemistrySelect. 6:6295-6301
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9287f23a7c37120496e673656ae476de
https://doi.org/10.1002/slct.202101990
https://doi.org/10.1002/slct.202101990