Articles - Sciact

Articles (90)

#	Публикация
41	Starosotnikov A.M. , Bastrakov M.A. , Kachala V.V. , Fedyanin I.V. , Shevelev S.A. , Dalinger I.L. Unusual Pericyclic Reactivity of 4‐Nitrobenzofuroxans in 1,3‐Dipolar Cycloaddition with N‐Benzyl Azomethine Ylide – A New Example of Multiple C–C‐Bond Forming Transformations. ChemistrySelect. 2018. V.3. N34. P.9773-9777. DOI: 10.1002/slct.201802117 WOS Scopus OpenAlex
42	Starosotnikov A.M. , Nikol'skiy V.V. , Bastrakov M.A. , Kachala V.V. , Pavlov A.A. , Ugrak B.I. , Shevelev S.A. Synthesis of Pyrido[2, 3‐a]phenoxazines and Pyrido[2, 3‐a]phenothiazines via Successive SNAr Processes ChemistrySelect. 2018. V.3. N4. P.1230-1233. DOI: 10.1002/slct.201702806 WOS Scopus OpenAlex
43	Starosotnikov A.M. , Shkaev D.V. , Bastrakov M.A. , Fedyanin I.V. , Shevelev S.A. , Dalinger I.L. Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds Mendeleev Communications. 2018. V.28. N6. P.638-640. DOI: 10.1016/j.mencom.2018.11.025 WOS Scopus OpenAlex
44	Bastrakov M.A. , Starosotnikov A.M. Pyrrole ring closure reactions in the synthesis of isoindoles (microreview) Chemistry of Heterocyclic Compounds. 2018. V.54. N10. P.926-928. DOI: 10.1007/s10593-018-2371-2 WOS Scopus OpenAlex
45	Starosotnikov A.M. , Bastrakov M.A. Cycloaddition reactions in the synthesis of isoindolines (microreview) Chemistry of Heterocyclic Compounds. 2017. V.53. N11. P.1181-1183. DOI: 10.1007/s10593-018-2191-4 WOS Scopus OpenAlex
46	Korolev S.P. , Pustovarova M.A. , Starosotnikov A.M. , Bastrakov M.A. , Agapkina Y.Y. , Shevelev S.A. , Gottikh M.B. Nitrobenzofuroxane derivatives as dual action HIV-1 inhibitors Biochemistry (Moscow). Supplement Series B: Biomedical Chemistry. 2017. V.11. N3. P.286-290. DOI: 10.1134/s1990750817030064 WOS Scopus OpenAlex
47	Bastrakov M.A. , Kucherova A.Y. , Fedorenko A.K. , Starosotnikov A.M. , Fedyanin I.V. , Dalinger I.L. , Shevelev S.A. Dearomatization of 3,5-dinitropyridines – an atom-efficient approach to fused 3-nitropyrrolidines Arkivoc. 2017. N3. P.181-190. DOI: 10.24820/ark.5550190.p010.185 Scopus OpenAlex
48	Starosotnikov A.M. , Shkaev D.V. , Bastrakov M.A. , Fedyanin I.V. , Shevelev S.A. , Dalinger I.L. Nucleophilic dearomatization of 4-aza-6-nitrobenzofuroxan by CH acids in the synthesis of pharmacology-oriented compounds Beilstein Journal of Organic Chemistry. 2017. V.13. P.2854-2861. DOI: 10.3762/bjoc.13.277 WOS Scopus OpenAlex
49	Starosotnikov A.M. , Bastrakov M.A. , Pavlov A.A. , Fedyanin I.V. , Dalinger I.L. , Shevelev S.A. Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan Mendeleev Communications. 2016. V.26. N3. P.217-219. DOI: 10.1016/j.mencom.2016.04.013 WOS Scopus OpenAlex
50	Bastrakov M.A. , Geraseva A.O. , Starosotnikov A.M. , Fedyanin I.V. , Pavlov A.A. , Ugrak B.I. , Shevelev S.A. Synthesis of nitro pyrido- and dipyrido[1,4]oxazines Mendeleev Communications. 2016. V.26. N5. P.383-385. DOI: 10.1016/j.mencom.2016.09.005 WOS Scopus OpenAlex
51	Korolev S.P. , Pustovarova M.A. , Starosotnikov A.M. , Bastrakov M.A. , Agapkina Y.Y. , Shevelev S.A. , Gottikh M.B. Nitrobenzofuroxane derivatives as dual action HIV-1 inhibitors Биомедицинская химия. 2016. V.62. N6. P.725-728. DOI: 10.18097/pbmc20166206725 Scopus OpenAlex
52	Bastrakov M.A. , Starosotnikov A.M. , Pavlov A.A. , Dalinger I.L. , Shevelev S.A. Synthesis of novel polycyclic heterosystems from 5-nitro[1,2,5]selenadiazolo[3,4-e]benzofuroxans Chemistry of Heterocyclic Compounds. 2016. V.52. N9. P.690-693. DOI: 10.1007/s10593-016-1950-3 WOS Scopus OpenAlex
53	Starosotnikov A.M. , Nikol'skiy V.V. , Borodulya A.N. , Kachala V.V. , Bastrakov M.A. , Solkan V.N. , Shevelev S.A. Synthesis and Functionalization of 5,7‐Dinitroquinoline and Its N‐Oxide Asian Journal of Organic Chemistry. 2016. V.5. N5. P.685-690. DOI: 10.1002/ajoc.201600065 WOS Scopus OpenAlex
54	Bastrakov M.A. , Starosotnikov A.M. , Kachala V.V. , Dalinger I.L. , Shevelev S.A. 3-R-4-Nitro-6,7-furoxanobenzo[d]isoxazoles – a new type of condensed nitroarenes capable of Diels–Alder reaction Chemistry of Heterocyclic Compounds. 2015. V.51. N5. P.496-499. DOI: 10.1007/s10593-015-1726-1 WOS Scopus OpenAlex
55	Steglenko D.V. , Shevelev S.A. , Kletskii M.E. , Burov O.N. , Lisovin A.V. , Starosotnikov A.M. , Morozov P.G. , Kurbatov S.V. , Minkin V.I. , Bastrakov M.A. Quantum-chemical and NMR study of nitrofuroxanoquinoline cycloaddition Chemistry of Heterocyclic Compounds. 2015. V.51. N9. P.845-857. DOI: 10.1007/s10593-015-1785-3 WOS Scopus OpenAlex
56	Bastrakov M.A. , Starosotnikov A.M. , Kachala V.V. , Fedyanin I.V. , Shevelev S.A. Facile Dearomatization of Nitroquinolines through [3+2] and [4+2] Cycloaddition Reactions Asian Journal of Organic Chemistry. 2015. V.4. N2. P.146-153. DOI: 10.1002/ajoc.201402207 WOS Scopus OpenAlex
57	Shevelev S. , Starosotnikov A. Direct Functionalization of C–H Fragments in Nitroarenes as a Synthetic Pathway to Condensed N-Heterocycles In compilation Metal Free C-H Functionalization of Aromatics. – Springer Cham., 2013. – C.107-154. – ISBN 978-3-319-07019-3. DOI: 10.1007/7081_2013_112 OpenAlex
58	Bastrakov M.A. , Leonov A.I. , Starosotnikov A.M. , Fedyanin I.V. , Shevelev S.A. 8-R-5,7-Dinitroquinolines in [3+2] cycloaddition reactions with N-methylazomethine ylide Russian Chemical Bulletin. 2013. V.62. N4. P.1052-1059. DOI: 10.1007/s11172-013-0141-y WOS Scopus OpenAlex
59	Korolev S.P. , Kondrashina O.V. , Druzhilovsky D.S. , Starosotnikov A.M. , Dutov M.D. , Bastrakov M.A. , Dalinger I.L. , Filimonov D.A. , Shevelev S.A. , Poroikov V.V. , Agapkina Y.Y. , Gottikh M.B. Structural-Functional Analysis of 2,1,3-Benzoxadiazoles and Their N-oxides As HIV-1 Integrase Inhibitors Acta Naturae. 2013. V.5. N1. P.63-72. DOI: 10.32607/20758251-2013-5-1-63-72 WOS Scopus OpenAlex
60	Shevelev S.A. , Starosotnikov A.M. Pericyclic [4+2] and [3+2] Cycloaddition Reactions of Nitroarenes in Heterocyclic Synthesis Chemistry of Heterocyclic Compounds. 2013. V.49. N1. P.92-115. DOI: 10.1007/s10593-013-1233-1 WOS Scopus OpenAlex

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