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81
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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
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82
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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
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83
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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
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84
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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
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85
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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
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86
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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
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Scopus
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87
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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
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88
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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
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89
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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
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90
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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
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91
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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
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92
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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.
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93
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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
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94
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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
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95
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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
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96
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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
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97
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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
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98
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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
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99
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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
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100
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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.
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