Zobrazeno 1 - 10
of 13
pro vyhledávání: '"K. S. Denisova"'
Autor:
V. V. Bocharov, K. S. Denisova
Publikováno v:
Обозрение психиатрии и медицинской психологии имени В.М. Бехтерева, Vol 0, Iss 1, Pp 31-36 (2018)
The article represents the results of the research of personality characteristics of men who serves in security police units with «pre-disease» somatic health disorders. The sample includes 112 men (length of service from 7 to 15 years), found fit
Externí odkaz:
https://doaj.org/article/b53e842188234d08b7f56ed47b1e3213
Autor:
V. A. Vydrina, Marina P. Yakovleva, Alexander G. Tolstikov, G. Yu. Ishmuratov, K. S. Denisova
Publikováno v:
Russian Journal of Organic Chemistry. 57:679-729
The review describes the most common macrolactonization reactions, including the activation of one and/or another terminal functional group in a seco acid in the synthesis of natural and biologically active compounds, and also analyzes the advantages
Autor:
Marina P. Yakovleva, G. Yu. Ishmuratov, V. A. Vydrina, Alexander G. Tolstikov, E. M. Vyrypaev, K. S. Denisova
Publikováno v:
Russian Journal of Organic Chemistry. 56:2236-2239
Efficient methods have been developed for the synthesis of three potentially useful macroheterocycles containing pyridine-2,6-dicarboxylic and adipic acid ester and hydrazide fragments starting from tetrahydropyran (commercial petrochemical product)
Autor:
G. Yu. Ishmuratov, Yu. V. Myasoedova, K. S. Denisova, Marina P. Yakovleva, N. M. Ishmuratova, G. R. Mingaleeva, L. R. Garifullina
Publikováno v:
Chemistry of Natural Compounds. 56:487-491
Efficient syntheses of six potentially useful optically pure macroheterocycles with ester and dihydrazide fragments were developed from available natural Δ3-carene through intermediate (31R,33S)-32,32-dimethyl-3(1,3)cyclopropyla-5-oxohexanoic acid u
Publikováno v:
Macroheterocycles. 13:79-82
Publikováno v:
Russian Chemical Bulletin. 68:1445-1450
Six optically active macroheterocycles bearing ester and dihydrazide moieties were synthesized from available natural (-)-α-pinene through the intermediate keto acid, (31R,33R)- 1-hydroxy-32,32-dimethyl-1,4-dioxopentaphane, using the [2+1] reaction
Publikováno v:
Chemistry of Natural Compounds. 54:889-892
Effective syntheses of three optically active macroheterocycles with ester, azine, and dihydrazide fragments were developed from available natural L-menthol through intermediate 3R,7-dimethyl-6-oxooctanoic acid using [2 + 1]-reaction of the last with
Autor:
Marina P. Yakovleva, G. Yu. Ishmuratov, E. M. Vyrypaev, A. A. Kravchenko, K. S. Denisova, G. R. Mingaleeva
Publikováno v:
Chemistry of Natural Compounds. 54:684-687
A mixture of cyclic lactones [7- (mentholactone), 14-, 21-, 28-, and 35-membered polylactones] instead of the expected [2 + 1]-condensation products was obtained from the reaction of 3R,7-dimethyl-6Shydroxyoctanoic acid, which is accessible from l-me
Autor:
Aleksandr G. Tolstikov, Marina P. Yakovleva, Gumer Yu. Ishmuratov, Timur R. Nugumanov, K. S. Denisova, G. R. Mingaleeva
Publikováno v:
Macroheterocycles. 11:193-196
Autor:
Alexander G. Tolstikov, E. M. Vyrypaev, R. R. Vil′danova, K. S. Denisova, R. R. Sayakhov, V. A. Vydrina, G. Yu. Ishmuratov, Marina P. Yakovleva
Publikováno v:
Chemistry of Natural Compounds. 53:620-622
A one-step synthesis of potentially useful enantiomerically pure macroheterocycles with four esters was developed starting from natural castor oil [(R,Z)-(+)-12-hydroxy-9-octadecenoic acid triglyceride].