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Статьи (359)

# Публикация
81 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 OpenAlex
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 OpenAlex
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 OpenAlex
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 OpenAlex
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 OpenAlex
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 OpenAlex
87 Крысин А.П. , Толстикова Т.Г. , Долгих М.П. , Шульц Э.Э. , Покровский Л.М.
Синтез и противовоспалительная активность тирозола и его структурных аналогов
Химико-фармацевтический журнал (PHARM CHEM J+). 2018. Т.52. №11. С.32-36. DOI: 10.30906/0023-1134-2018-52-11-32-36 РИНЦ OpenAlex
88 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 OpenAlex
89 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 OpenAlex
90 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
91 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 OpenAlex
92 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 OpenAlex
93 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.
94 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 OpenAlex
95 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 OpenAlex
96 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 OpenAlex
97 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 OpenAlex
98 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 OpenAlex
99 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 OpenAlex
100 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 OpenAlex

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