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1
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Shpatov A.V.
, Zakharova S.S.
, Popov S.A.
Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles
Chemistry of Natural Compounds. 2022.
V.58. N2. P.290-296. DOI: 10.1007/s10600-022-03662-5
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2
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Shpatov A.V.
, Frolova T.S.
, Popov S.A.
, Sinitsyna O.I.
, Salnikova O.I.
, Zheng G.
, Yan L.
, Sinelnikova N.V.
, Pshennikova L.M.
, Kochetov A.V.
Lipophilic Metabolites from Five-Needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity
Chemistry and Biodiversity. 2020.
V.17. N8. e2000201
. DOI: 10.1002/cbdv.202000201
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3
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Pyatrikas D.V.
, Gorbyleva E.L.
, Fedyaeva A.V.
, Zakharova S.S.
, Shpatov A.V.
, Popov S.A.
, Borovskii G.B.
Search for biologically active substances of natural origin based on low-polar conifer extracts
Известия вузов. Прикладная химия и биотехнология. 2020.
V.10. N2. P.240-250. DOI: 10.21285/2227-2925-2020-10-2-240-250
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4
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Popov S.A.
, Kornaukhova L.M.
, Shpatov A.V.
, Grigore'ev I.A.
Synthesis of Conjugates of Ursolic Acid 3-O-Succinate with NO-H2S Donors
Chemistry of Natural Compounds. 2017.
V.53. N3. P.592-594. DOI: 10.1007/s10600-017-2061-9
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5
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Shpatov A.V.
, Popov S.A.
, Salnikova O.I.
, Kukina T.P.
, Shmidt E.N.
, Um B.H.
Composition and Bioactivity of Lipophilic Metabolites from Needles and Twigs of Korean and Siberian Pines (Pinus koraiensis Siebold & Zucc. and Pinus sibirica Du Tour)
Chemistry and Biodiversity. 2017.
V.14. N2. e1600203
. DOI: 10.1002/cbdv.201600203
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6
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Popov S.A.
, Kornaukhova L.M.
, Shpatov A.V.
, Grigor'ev I.A.
Synthesis of Ursolic Acid Conjugates Containing a Furoxan Moiety
Chemistry of Natural Compounds. 2016.
V.52. N3. P.555-557. DOI: 10.1007/s10600-016-1708-2
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РИНЦ
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7
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Popov S.A.
, Kornaukhova L.M.
, Shpatov A.V.
, Grigor'ev I.A.
Synthesis of Conjugate Esters of 5-(4-Hydroxyphenyl)-3H-1,2-Dithiole-3-Thione and Ursolic Acid 3-O-ACYL Derivatives
Chemistry of Natural Compounds. 2016.
V.52. N1. P.183-185. DOI: 10.1007/s10600-016-1588-5
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РИНЦ
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8
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Popov S.A.
, Kozlova L.P.
, Kornaukhova L.M.
, Shpatov A.V.
Simple and efficient process for large scale preparation of betulonic acid from birch bark extracts
Industrial Crops and Products. 2016.
V.92. P.197-200. DOI: 10.1016/j.indcrop.2016.07.026
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РИНЦ
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9
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Popov S.A.
, Shpatov A.V.
, Grigor'ev I.A.
Synthesis of Substituted Esters of Ursolic, Betulonic, and Betulinic Acids Containing the Nitroxyl Radical 4-Amino-2,2,6,6-Tetramethylpiperidine-1-Oxyl
Chemistry of Natural Compounds. 2015.
V.51. N1. P.87-90. DOI: 10.1007/s10600-015-1209-8
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РИНЦ
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10
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Popov S.A.
, Shpatov A.V.
, Grigor'Ev I.A.
Erratum: Synthesis of Substituted Esters of Ursolic, Betulonic, and Betulinic Acids Containing the Nitroxyl Radical 4-Amino-2,2,6,6-Tetramethylpiperidine-1-Oxyl (Chemistry of Natural Compounds (2015) 51:1 (87-90))
Chemistry of Natural Compounds. 2015.
V.51. N2. P.402-. DOI: 10.1007/s10600-015-1300-1
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11
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Khokhrina E.A.
, Shpatov A.V.
, Popov S.A.
, Sal'nikova O.I.
, Shmidt E.N.
, Um B.H.
Non-Volatile Compounds of Needles, Trimmed Saplings, and Outer Bark of Pinus densiflora
Chemistry of Natural Compounds. 2013.
V.49. N3. P.561-565. DOI: 10.1007/s10600-013-0673-2
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РИНЦ
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12
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Shpatov A.V.
, Popov S.A.
, Salnikova O.I.
, Shmidt E.N.
, Kang S.W.
, Kim S.M.
, Um B.H.
Lipophilic Extracts from Needles and Defoliated Twigs of Pinus pumila from Two Different Populations
Chemistry and Biodiversity. 2013.
V.10. N2. P.198-208. DOI: 10.1002/cbdv.201200009
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РИНЦ
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13
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Shpatov A.V.
, Popov S.A.
, Salnikova O.I.
, Khokhrina E.A.
, Shmidt E.N.
, Um B.H.
Low-Volatile Lipophilic Compounds in Needles, Defoliated Twigs, and Outer Bark of Pinus thunbergii
Natural Product Communications. 2013.
V.8. N12. P.1759-1762. DOI: 10.1177/1934578x1300801227
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РИНЦ
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14
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Lee C.W.
, Park N.H.
, Kim J.W.
, Um B.H.
, Shpatov A.V.
, Shults E.E.
, Sorokina I.V.
, Popov S.A.
Study of skin anti-ageing and anti-inflammatory effects of dihydroquercetin, natural triterpenoinds, and their synthetic derivatives
Russian Journal of Bioorganic Chemistry. 2012.
V.38. N3. P.328-334. DOI: 10.1134/S1068162012030028
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15
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Попов С.А.
, Глинская Л.А.
, Кокина Т.Е.
, Клевцова Р.Ф.
, Шпатов А.В.
КРИСТАЛЛИЧЕСКАЯ И МОЛЕКУЛЯРНАЯ СТРУКТУРА 3,5-ДИМЕТИЛ-1H-ПИРАЗОЛИДА 3-O-АЦЕТИЛУРСОЛОВОЙ КИСЛОТЫ
Журнал структурной химии (J STRUCT CHEM+). 2011.
Т.52. №3. С.599-604.
РИНЦ
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16
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Lee E.H.
, Popov S.A.
, Lee J.Y.
, Shpatov A.V.
, Kukina T.P.
, Kang S.W.
, Pan C.H.
, Um B.H.
, Jung S.H.
Inhibitory effect of ursolic acid derivatives on recombinant human aldose reductase
Russian Journal of Bioorganic Chemistry. 2011.
V.37. N5. P.569-577. DOI: 10.1134/S1068162011050050
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17
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Popov S.A.
, Glinskaya L.A.
, Kokina T.E.
, Klevtsova R.F.
, Shpatov A.V.
Crystal and molecular structure of 3,5-dimethyl-1H-pyrazolide of 3-o-acetyl ursolic acid
Journal of Structural Chemistry. 2011.
V.52. N3. P.582-588. DOI: 10.1134/S0022476611030206
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РИНЦ
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18
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Shpatov A.V.
, Shakirov M.M.
, Raldugin V.A.
Cyclization of cembrane diterpenoids: IX. Electrophilic cyclization of 5α-acetoxyisocembrol
Russian Journal of Organic Chemistry. 2000.
V.36. N8. P.1127-1138.
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19
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Shpatov A.V.
, Shakirov M.M.
, Gatilov Y.V.
, Rybalova T.V.
, Raldugin V.A.
Cyclization of Cembrane Diterpenoids: VIII. Acid-catalyzed Cyclization of Isocembrol
Russian Journal of Organic Chemistry. 1997.
V.33. N2. P.194-204.
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РИНЦ
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20
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Shpatov A.V.
, Shakirov M.M.
, Gatilov Y.V.
, Rybalova T.V.
, Raldugin V.A.
Cyclization of cembrane diterpenoids .8. Acid-catalyzed cyclization of isocembrole
Журнал органической химии (RUSS J ORG CHEM+). 1997.
V.33. N2. P.224-235.
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