Zobrazeno 1 - 10
of 45
pro vyhledávání: '"M. F. Larin"'
Autor:
V. A. Pestunowich, M. F. Larin, Harald Jancke, M. G. Voronkov, E. I. Dubinskaja, Heinrich Kriegsmann, Günter Engelhardt, Reiner Radeglia
Publikováno v:
Zeitschrift für Chemie. 17:376-376
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3de7d5a2cec652bd4aaa394f082c69dd
https://doi.org/10.1002/zfch.19770171016
https://doi.org/10.1002/zfch.19770171016
Autor:
V. Chvalovsky, H. Jancke, P. Koehler, M. F. Larin, V. A. Pestunovich, M. G. Voronkov, Jan Schraml
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3c987ff58d80bd1cdcbaa6392085388
https://doi.org/10.1002/chin.199049047
https://doi.org/10.1002/chin.199049047
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c90226b072213adb926f57aeb9c7048c
https://doi.org/10.1002/chin.199039257
https://doi.org/10.1002/chin.199039257
Autor:
Lyudmila I. Larina, V. A. Lopyrev, M. F. Larin, O. B. Nefedova, Tamara I. Vakul'skaya, M. G. Voronkov, E. F. Shibanova
Publikováno v:
Organic Magnetic Resonance. 15:219-224
The substituent influence on the 1H and 13C NMR chemical shifts in 2-substituted benzimidazoles and their anions and cations has been investigated. The transmission of the electronic effects of substituents from C-2 to C-5 (6) is approximately 20% le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9686ec0eccaecd94c75277de9792c36b
https://doi.org/10.1002/mrc.1270150302
https://doi.org/10.1002/mrc.1270150302
Publikováno v:
Chemistry of Natural Compounds. 23:310-316
Squarrofuric acid has been isolated fromThalictrum squarrosum by the acid hydryolysis of a methanolic extract. It is suggested that is is an artefact formed on hydrolysis and has the structure of 3β, 30-dihydroxy-22,25-epoxylanost-9(11)-en-21-oic ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e7c3831a71911b57190e8b3f40052cd
https://doi.org/10.1007/bf00600830
https://doi.org/10.1007/bf00600830
Publikováno v:
Polymer Science U.S.S.R.. 25:2203-2212
The polymerization of 10-vinylphenothiazine in the presence of tetrahalobenzoquinones is shown to be an autocatalytic process. The polymerization is catalyzed by hydrogen halide formed as a result of interaction between monomer and initiator. The pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::727b4ae88e148d4cd19534faa210338e
https://doi.org/10.1016/0032-3950(83)90417-3
https://doi.org/10.1016/0032-3950(83)90417-3
Autor:
T. V. Ganenko, M. I. Isaev, A. S. Gromova, N. D. Abdullaev, V. I. Lutskii, M. F. Larin, A. A. Semenov, M. B. Gorovits, N. K. Abubakirov
Publikováno v:
Chemistry of Natural Compounds. 22:288-294
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::380480874eedcb84a62bb64d87721c09
https://doi.org/10.1007/bf00598298
https://doi.org/10.1007/bf00598298
Autor:
Lyudmila I. Larina, M. G. Voronkov, E. E. Liepin'sh, I. A. Titova, Tamara I. Vakul'skaya, E. F. Shibanova, V. A. Lopyrev, M. F. Larin
Publikováno v:
Magnetic Resonance in Chemistry. 23:301-304
The influence of substituents on the 1H, 13C and 15N NMR chemical shifts of 2-substituted 5(6)-nitrobenzimidazoles and their analogues labelled with 15N in the nitro group was investigated. It was found that the substituent effects are transmitted to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d7f9a99c18c3b096d17641d2b81f4f7
https://doi.org/10.1002/mrc.1260230505
https://doi.org/10.1002/mrc.1260230505
Publikováno v:
Chemistry of Natural Compounds. 25:573-576
A new triterpene pentaglycoside — medicoside L — has been isolated from the roots ofMedicago sativa L. (Leguminosae). It has the structure of medicagenic acid 28-O-β-D-glucopyranoside 3-O-{[O-β-D-glucopyranosyl-(1 → 2)][O-α-L-rhamnopyranosyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebaa192f78abf723cf40870f7f940d58
https://doi.org/10.1007/bf00598078
https://doi.org/10.1007/bf00598078
Autor:
E.I. Brodskaya, M. F. Larin, V. Yu. Vitkovskii, R. G. Mirskov, S. V. Basenko, V. A. Pestunovich, M. G. Voronkov, D. D. Toryashinova
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 34:2056-2060
The IR, UV, NMR, and mass spectra of silyl-substituted alkylthioacetates have been investigated. Intramolecular coordination of the carbonyl group with the silicon atom has been shown to exist in molecules of trifluoroaeetylthiomethylsilane in the co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb4e754bfaeda9976e7debc8a5bd144d
https://doi.org/10.1007/bf00963232
https://doi.org/10.1007/bf00963232