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Tolstikov Genrikh A

Researcher at Russian Academy of Sciences

Publications -  1346
Citations -  5730

Tolstikov Genrikh A is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Catalysis & Ozonolysis. The author has an hindex of 27, co-authored 1346 publications receiving 5222 citations. Previous affiliations of Tolstikov Genrikh A include Bashkir State University.

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Synthetic transformations of higher terpenoids. XXVI. 16-acetylaminomethyllabdanoids and their cytotoxicity

Yu. V. Kharitonov, +5 more
- 28 Jan 2012 - 
TL;DR: The compounds obtained were more cytotoxic toward CEM-13, MT-4, and U-937 tumor cell lines as compared with lambertianic acid; the dose inhibiting tumor cell viability by 50% (CCID50) of the more active compounds was 3.9–9.9 μM.
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Study of alkaloids from the flora of the Siberian and Altai regions. 6. Crystal and molecular structure of songorine Z-oxime

I. Yu. Bagryanskaya, +6 more
- 01 Nov 2001 - 
TL;DR: In this paper, the crystal and molecular structure of the Z-isomer was established by X-ray diffraction analysis and its structure was also confirmed by the spectral data (2D 1H, 1H and 13C, NMR spectroscopy and mass spectrometry).
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First synthesis of steroidal 1,2,4-trioxolanes

E. Yu. Yamansarov, +5 more
- 13 Aug 2014 - 
TL;DR: Griesbaum ozonolysis of mixtures of methyl 3-(methoxyimino)-5β-cholan-24-oate with ketones (cyclohexanone, methyl trifluoromethyl ketone, and phenyl triflormethemethyl ketone) enabled for the first time steroidal 1,2,4-trioxolanes which were isolated as mixtures OF stereoisomers as mentioned in this paper.
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A one-step approach to the synthesis of germanicane triterpenoids from allobetulin

Oxana B. Kazakova, +2 more
- 02 Feb 2010 - 
TL;DR: A new triterpenoid of the germanicane series 3S,19R-diacetoxy-17-iodomethylenoleanane has been synthesized by treating allobetulin with acetyl chloride and sodium iodide in acetonitrile.
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New type of interaction of 5-iodopyrimidine nucleosides with alkynes

Tolstikov Genrikh A, +5 more
- 01 Mar 1993 - 
Abstract: The interaction of 1-(β-D-xylofuranosyl)-5-iodo(bromo)uracil derivatives with terminal alkynes in the presence of catalytic amounts of 10% Pd/C and Cul affords the corresponding derivatives of 3-(β-D-xylofuranosyl)-6-R-furo[2, 3-d]pyrimidin-2-ones in high yields.