Persons
RUS  ENG    JOURNALS   PEOPLE   ORGANISATIONS   CONFERENCES   SEMINARS   VIDEO LIBRARY   PACKAGE AMSBIB  
 
Stepanov, Andrei Valentinovich

E-mail:

https://www.mathnet.ru/eng/person77827
List of publications on Google Scholar

Publications in Math-Net.Ru Citations
2024
1. K. V. Agliulin, A. V. Stepanov, V. N. Yarovenko, M. M. Krayushkin, E. V. Tretyakov, D. I. Nasyrova, V. V. Ilyushenkova, A. O. Ayt, T. M. Valova, “Synthesis, structure and properties of spin-labeled photosensitive chromone derivative”, Mendeleev Commun., 34:6 (2024),  828–830  mathnet  scopus
2018
2. A. V. Stepanov, C. E. Mel'nik, V. I. Isaeva, G. I. Kapustin, V. V. Chernyshev, V. V. Veselovsky, “The Henry reaction catalyzed by zeolitic imidazolate framework ZIF-8”, Mendeleev Commun., 28:1 (2018),  88–90  mathnet  scopus 11
2013
3. V. A. Popovsky, A. V. Stepanov, N. Ya. Grigorieva, “Total synthesis of strobilurin B”, Mendeleev Commun., 23:4 (2013),  190–192  mathnet  scopus 3
2012
4. V. V. Veselovsky, A. V. Lozanova, A. V. Stepanov, “A New Approach to the Synthesis of 15-A<sub>2t</sub>IsoP Isoprostane and 14-A<sub>4t</sub>NeuroP Neuroprostane”, Mendeleev Commun., 22:5 (2012),  252–253  mathnet  scopus 7
2008
5. A. V. Stepanov, E. A. Mistryukov, “Aluminium–isopropanol reduction of <i>tert</i>-nitronitriles: an unusual structure of the reduction products”, Mendeleev Commun., 18:4 (2008),  215–216  mathnet  scopus 1
6. N. Ya. Grigorieva, A. G. Smirnov, V. A. Popovsky, A. V. Stepanov, “Stereoselective synthesis of key intermediates for the preparation of strobilurins”, Mendeleev Commun., 18:2 (2008),  84–85  mathnet  scopus 6
2006
7. A. V. Lozanova, T. M. Ugurchieva, M. V. Zlokazov, A. V. Stepanov, V. V. Veselovsky, “Stereoselective formation of a 3,5-<i>trans</i>-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide”, Mendeleev Commun., 16:1 (2006),  15–16  mathnet  scopus 8
2003
8. A. V. Stepanov, V. V. Veselovsky, “Reactions of alkenes with nitrogen oxides and other nitrosating and nitrating reagents”, Usp. Khim., 72:4 (2003),  363–378  mathnet; Russian Chem. Reviews, 72:4 (2003), 327–341  isi  scopus 40

Organisations