Articles - Sciact

Articles (359)

#	Публикация
81	Cheremnykh K.P. , Savel'ev V.A. , Shkurko O.P. , Shults E.E. Synthesis of hybrid molecules containing pyrimidine and diterpene alkaloid lappaconitine fragments Chemistry of Heterocyclic Compounds. 2018. V.54. N12. P.1131-1138. DOI: 10.1007/s10593-019-02404-w WOS Scopus РИНЦ
82	Gromova M.A. , Kharitonov Y.V. , Bagryanskaya I.Y. , Shults E.E. Efficient Synthesis of the N-(buta-2,3-dienyl)carboxamide of Isopimaric Acid and the Potential of This Compound towards Heterocyclic Derivatives of Diterpenoids ChemistryOpen. 2018. V.7. N11. P.890-901. DOI: 10.1002/open.201800205 WOS Scopus РИНЦ
83	Grazhdannikov A.E. , Kornaukhova L.M. , Rodionov V.I. , Pankrushina N.A. , Shults E.E. , Fabiano-Tixier A.S. , Popov S.A. , Chemat F. Selecting a Green Strategy on Extraction of Birch Bark and Isolation of Pure Betulin Using Monoterpenes ACS Sustainable Chemistry and Engineering. 2018. V.6. N5. P.6281-6288. DOI: 10.1021/acssuschemeng.8b00086 WOS Scopus РИНЦ
84	Finke A.O. , Mironov M.E. , Skorova A.B. , Shults E.E. Copper-catalyzed 1,3-dipolar cycloaddition reaction of spirosolanederived azide for the preparation of modified solasodine alkaloid Chemistry of Heterocyclic Compounds. 2018. V.54. N4. P.411-416. DOI: 10.1007/s10593-018-2284-0 WOS Scopus РИНЦ
85	Gromova M.A. , Kharitonov Y.V. , Rybalova T.V. , Shul'ts E.E. *Synthetic Transformations of Higher Terpenoids. 36.() Synthesis of 13-(Oxazol-5-Yl)-15,16-Bisnorisopimaranes** Chemistry of Natural Compounds. 2018. V.54. N2. P.293-300. DOI: 10.1007/s10600-018-2327-x WOS Scopus РИНЦ
86	Kharitonov Y.V. , Shakirov M.M. , Shults E.E. Highly Selective Gold-Catalyzed Cycloisomerization of Furanolabdanoid Dialkynes with Alkynyl Substituents in the Furan Ring Current Organic Synthesis. 2018. V.15. N8. P.1147-1153. DOI: 10.2174/1570179415666180918160421 WOS Scopus РИНЦ
87	Bryzgalov A.O. , Tolstikova T.G. , Shults E.E. , Petrova K.O. Natural Products as a Source of Antiarrhythmic Drugs Mini-Reviews in Medicinal Chemistry. 2018. V.18. N4. P.345-362. DOI: 10.2174/1389557516666161104144815 WOS Scopus РИНЦ
88	Baysarov G.M. , Zhumatayeva A.R. , Mukusheva G.K. , Shul'ts E.E. , Seydakhmetova R.B. , Adekenov S.M. Flavonoid compounds from Artemisia glabella Kar. Et. Kir., synthesis on their basis and biological activity Химия растительного сырья. 2018. N3. P.215-222. DOI: 10.14258/jcprm.2018033766 Scopus РИНЦ
89	Lipeeva A.V. , Shults E.E. *A study of plant coumarins 16. Synthesis and transformations of 7-alkynylcoumarins** Chemistry of Heterocyclic Compounds. 2017. V.53. N12. P.1302-1309. DOI: 10.1007/s10593-018-2210-5 WOS Scopus РИНЦ
90	Kremenko O.I. , Kharitonov Y.V. , Shul'ts E.E. Synthetic Transformations of Higher Terpenoids: XXXVI.(1) Synthesis of Furanolabdanoid Glycoconjugates with a 1,2,3-Triazole Linker Russian Journal of Organic Chemistry. 2017. V.53. N1. P.35-46. DOI: 10.1134/S1070428017010079 WOS Scopus РИНЦ
91	Urbagarova B.M. , Taraskin V.V. , Shul'ts E.E. , Radnaeva L.D. , Anenkhonov O.A. , Ganbaatar Z. , Boldanova N.B. Biologically Active Compounds from the Lipid Fraction of Saposhnikovia divaricata Chemistry of Natural Compounds. 2017. V.53. N1. P.138-140. DOI: 10.1007/s10600-017-1928-0 WOS Scopus РИНЦ
92	Брусенцева О.И. , Харитонов Ю.В. , Шульц Э.Э. Синтетические трансформации высших терпеноидов. xxxvi. синтез гликоконъюгатов фуранолабданоидов с 1,2,3-триазольным линкером Журнал органической химии (RUSS J ORG CHEM+). 2017. Т.53. №1. С.42-52. РИНЦ
93	Bauman V.T. , Ganbaatar J. , Shults E.E. Synthetic transformations of isoquinoline alkaloids: 1-(N-alkyl-1,2,3-triazol-4-yl)-6,18-endo-ethenodihydrothebainehydroquinones and triazolylnaphthohydroquinone-containing benzofuroazocines from thebaine Chemistry of Heterocyclic Compounds. 2017. V.53. N8. P.913-919. DOI: 10.1007/s10593-017-2145-2 WOS Scopus РИНЦ
94	Popov S.A. , Sheremet O.P. , Kornaukhova L.M. , Grazhdannikov A.E. , Shults E.E. An approach to effective green extraction of triterpenoids from outer birch bark using ethyl acetate with extractant recycle Industrial Crops and Products. 2017. V.102. P.122-132. DOI: 10.1016/j.indcrop.2017.03.020 WOS Scopus РИНЦ
95	Patrushev S.S. , Rybalova T.V. , Ivanov I.D. , Vavilin V.A. , Shults E.E. Synthesis of a new class of bisheterocycles via the Heck reaction of eudesmane type methylene lactones with 8-bromoxanthines Tetrahedron. 2017. V.73. N19. P.2717-2726. DOI: 10.1016/j.tet.2017.03.016 WOS Scopus РИНЦ
96	Shults E.E. , Shakirov M.M. , Pokrovsky M.A. , Petrova T.N. , Pokrovsky A.G. , Gorovoy P.G. Phenolic compounds from Glycyrrhiza pallidiflora Maxim. and their cytotoxic activity Natural Product Research. 2017. V.31. N4. P.445-452. DOI: 10.1080/14786419.2016.1188094 WOS Scopus РИНЦ
97	Lipeeva A.V. , Baev D.S. , Dolgikh M.P. , Tolstikova T.G. , Shults E.E. Rapid Access to Oxazine Fused Furocoumarins and in vivo and in silico Studies of theirs Biological Activity Medicinal Chemistry. 2017. V.13. N7. P.625-632. DOI: 10.2174/1573406413666170601114527 WOS Scopus РИНЦ
98	Kharitonov Y.V. , Shakirov M.M. , Shults E.E. Synthesis of Novel Labdanoid-Based Macroheterocycles Using Click-Cycloaddition Reaction Protocol Macroheterocycles. 2017. V.10. N1. P.117-122. DOI: 10.6060/mhc160959s WOS Scopus РИНЦ
99	Kharitonov Y.V. , Shakirov M.M. , Pokrovskii M.A. , Pokrovskii A.G. , Shu?Ts E.E. *Synthetic transformations of higher terpenoids. XXXV. synthesis and cytotoxicity of macroheterocyclic compounds based on lambertianic acid** Chemistry of Natural Compounds. 2017. V.53. N1. P.77-82. DOI: 10.1007/s10600-017-1915-5 WOS Scopus РИНЦ
100	Бурова Л.Г. , Широких И.В. , Патрушев С.С. , Толстикова Т.Г. , Шульц Э.Э. ВЗАИМОСВЯЗЬ СТРУКТУРА-АНТИБАКТЕРИАЛЬНАЯ АКТИВНОСТЬ В РЯДУ ПРОИЗВОДНЫХ ИЗОАЛАНТОЛАКТОНА ФУНДАМЕНТАЛЬНАЯ И КЛИНИЧЕСКАЯ МЕДИЦИНА. 2017. Т.2. №1. С.28-34.

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