Zobrazeno 1 - 10
of 23
pro vyhledávání: '"E E, Shul'ts"'
Publikováno v:
Chemistry of Natural Compounds. 58:65-70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5431d756b01624d33d32e2da75e98413
https://doi.org/10.1007/s10600-022-03597-x
https://doi.org/10.1007/s10600-022-03597-x
Autor:
M. A. Gromova, Yu. V. Kharitonov, S. A. Borisov, T. V. Rybalova, T. G. Tolstikova, E. E. Shul’ts
Publikováno v:
Chemistry of Natural Compounds. 58:55-64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ceb659b6e00b4ecf23291a66de1379f
https://doi.org/10.1007/s10600-022-03596-y
https://doi.org/10.1007/s10600-022-03596-y
Autor:
Zh. Ganbaatar, Larisa D. Radnaeva, B. M. Urbagarova, V. V. Taraskin, E. E. Shul′ts, Oleg A. Anenkhonov, N. B. Boldanova
Publikováno v:
Chemistry of Natural Compounds. 53:138-140
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60a506fffab365158534feae3c4e8485
https://doi.org/10.1007/s10600-017-1928-0
https://doi.org/10.1007/s10600-017-1928-0
Autor:
E. E. Shul′ts, V. E. Romanov
Publikováno v:
Chemistry of Natural Compounds. 51:1142-1146
New derivatives of the diterpene alkaloid lappaconitine containing a 1H-substituted 1,2,3-triazol-4-yl substituent in the anthranilate C-5 ′ -position were synthesized via the reaction of 5 ′ -ethynyllappaconitine with aromatic or aliphatic azide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c539dfb986fc36e3753dceedc2d768e4
https://doi.org/10.1007/s10600-015-1511-5
https://doi.org/10.1007/s10600-015-1511-5
Publikováno v:
Chemistry of Natural Compounds. 50:2-21
Structures of plant furanolabdanoids and synthetic schemes for a series of furanolabdanoids (coronarins A and E, hedychenone, acuminolide and 17-O-acetylacuminolide) from the available diterpenoids sclareol and larixol were reviewed. Attention was fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fbcf53dc903dc0e60fb0734a0d984d0
https://doi.org/10.1007/s10600-014-0861-8
https://doi.org/10.1007/s10600-014-0861-8
Autor:
Yu. V. Gatilov, E. E. Shul′ts, Yu. V. Kharitonov, I. Yu. Bagryanskaya, Makhmut M. Shakirov, Tolstikov Genrikh A
Publikováno v:
Chemistry of Natural Compounds. 48:250-257
Allylic oxidation of phlomisoic acid and its methyl ester by selenium dioxide occurred stereoselectively to form 7α-hydroxy derivatives of labdanoids, which were oxidized by active manganese dioxide to 7-ketofuranolabdanoids. Oximation of the last b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2493a58c590160d8f8988e01769cdee9
https://doi.org/10.1007/s10600-012-0215-3
https://doi.org/10.1007/s10600-012-0215-3
Publikováno v:
Russian Chemical Bulletin. 50:907-910
Elatidam, elatidamic acid, and elatidal were obtained for the first time by oxidation of the diterpene alkaloid elatidine with KMnO4 or CrO3 and characterized. The reactions of elatidal with hydroxylamine, aniline, allylamine, and methyl glycinate af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af24d2b6a0ff5f61d80c42463ec09776
https://doi.org/10.1023/a:1011379714369
https://doi.org/10.1023/a:1011379714369
Autor:
I. Yu. Bagryanskaya, A. V. Kazantsev, A. Zh. Turmukhambetov, E. E. Shul′ts, Makhmut M. Shakirov, M. T. Agedilova, Zh. S. Nurmaganbetov, S. M. Adekenov
Publikováno v:
Chemistry of Natural Compounds. 45:601-603
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::158841eb3be727d55be6aa7f3bca7f64
https://doi.org/10.1007/s10600-009-9381-3
https://doi.org/10.1007/s10600-009-9381-3
Publikováno v:
Chemistry of Natural Compounds. 44:740-742
The structure of 5′-bromolappaconitine that was synthesized by an alternate method was solved by XSA.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40c2580b9a2ca3082ffd709e7d867829
https://doi.org/10.1007/s10600-009-9186-4
https://doi.org/10.1007/s10600-009-9186-4
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86e521c3c9ee9bb52f838cbff83258db
https://doi.org/10.1002/chin.199816293
https://doi.org/10.1002/chin.199816293