Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Maria S. Volkova"'
Autor:
Maria S. Volkova, Alexander M. Efremov, Elena N. Bezsonova, Michael D. Tsymliakov, Anita I. Maksutova, Maria A. Salykina, Sergey E. Sosonyuk, Elena F. Shevtsova, Natalia A. Lozinskaya
Publikováno v:
Molecules, Vol 27, Iss 21, p 7462 (2022)
2,3-Dihydroindoles are promising agents for the synthesis of new compounds with neuroprotective and antioxidant properties. Usually, these compounds are obtained by direct reduction of the corresponding indoles containing acceptor groups in the indol
Externí odkaz:
https://doaj.org/article/8dbcec8864c348d69da9895ec2b97a5d
Autor:
Nataly B. Chesnokova, Nataly A. Lozinskaya, Maria S. Volkova, Nikolay S. Zefirov, Olga V. Beznos, Ekaterina V. Zaryanova
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 27:3787-3793
The study represents the new findings at the crossroads of chemistry and medicine, particularly between medicinal and organic chemistry and ophthalmology. In this work we describe how the chemical reactivity of indolinone scaffold may be used to crea
Autor:
Maria S. Volkova, Michael Yu. Seliverstov, S. E. Sosonyuk, N. A. Lozinskaya, Marina V. Proskurnina, Nikolay S. Zefirov, Sergey E. Bachurin
Publikováno v:
Synthesis. 2011:273-276
A simple strategy for the synthesis of some 2-substituted melatonin derivatives using p-anisidine as starting material is re- ported. The key step is a chemoselective reduction of a cyano group in the presence of an appropriate acid anhydride by hydr
Publikováno v:
IOP Conference Series: Materials Science and Engineering. 365:042053
Nonlinear vibration isolation systems have a wider range of effective damping than linear ones. However, their analysis with an arbitrary load is quite laborious. In the article the method of special selection of linear generating systems for analyzi
Autor:
Maria S. Volkova, Nikolay S. Zefirov, Marina V. Proskurnina, S. E. Sosonyuk, Andrew D. Mesecar, Katherine C. Jensen, N. A. Lozinskaya
Publikováno v:
Bioorganicmedicinal chemistry letters. 22(24)
New 5-acetamido-substituted melatonin derivatives were efficiently synthesized in excellent yields via Knoevenagel condensation. The relative binding affinity of new synthesized compounds to MT3 receptor was tested via enzymatic assays and the X-ray
Autor:
S. E. Sosonyuk, Michael Yu. Seliverstov, Marina V. Proskurnina, V. V. Temnov, Nikolai S. Zefirov, Maria S. Volkova, N. A. Lozinskaya
Publikováno v:
Mendeleev Communications. 24:260-261
2-(2-Oxo-1,2-dihydro-3H-indol-3-ylidene)acetonitriles were subjected to cycloaddition reactions at the double bond affording spiroindole melatonin analogues.