Search Results - "Muslukhov, R. R"

Hydroboration by Diborane of Methyl Abietate by Vydrina, V. A., Kravchenko, A. A., Yakovleva, M. P., Muslukhov, R. R., Tolstikov, A. G., Ishmuratov, G. Yu

“…Hydroboration-oxidation of methyl abietate by diborane in THF occurred preferentially at the sterically unhindered β -side of the molecule without involving…”
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Ozonolytic Transformation of (S)-(–)-Limonene in HCl–Isopropanol by Ishmuratov, G. Yu, Legostaeva, Yu. V, Garifullina, L. R, Muslukhov, R. R, Botsman, L. P, Kozlova, G. G

“…Partial ozonolysis of (S)-(–)-limonene (ee 50%) in cyclohexane:isopropanol at 2–4°C formed the 1,2,4-trioxolane as a mixture of diastereomers in a 3:2 ratio. A…”
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Synthetic Approaches to Optically Active Macrolides Containing Hydrazide Fragments of L-(+)-Tartaric Acid from (+)-3-Carene, (+)-α-Pinene, and S-(–)-Limonene by Ishmuratov, G. Yu, Yakovleva, M. P, Shutova, M. A, Muslukhov, R. R, Ishmuratova, N. M, Tolstikov, A. G

“…An optically pure macrolide containing 1,3-dioxolane, gem-dimethylcyclopropyl, and hydrazide fragments was synthesized from (+)-3-carene via [1+1]-condensation…”
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Dichlorocyclopropane derivatives of syndiotactic 1,2-polybutadiene by Glazyrin, A. B., Abdullin, M. I., Muslukhov, R. R.

“…Polymeric products containing hem-dichlorocyclopropane units with a degree of functionalization of up to 97% are synthesized via the reaction of syndiotactic…”
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Derivatives of syndiotactic cyclopropane-containing 1,2-polybutadiene by Glazyrin, A. B., Abdullin, M. I., Dokichev, V. A., Sultanova, R. M., Muslukhov, R. R., Gazizova, E. R.

“…The results of syndiotactic 1,2-polybutadiene cyclopropanation with diazomethane are demonstrated in an organic solvent in the presence of an organometallic…”
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(R)-n-menth-4-en-3-one and its Derivatives in Reactions with N-containing Reagents by Ishmuratov, G. Yu, Tukhvatshin, V. S, Yakovleva, M. P, Muslukhov, R. R, Allagulova, A. V, Talipova, G. R

“…The reactions of (R)-n-menth-4-en-3-one and its derivatives with N-containing reagents were studied. New menthane-type acetamides were synthesized…”
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Synthesis and properties of cyclopropane derivatives of polybutadienes by Glazyrin, A. B., Abdullin, M. I., Dokichev, V. A., Sultanova, R. M., Muslukhov, R. R., Yangirov, T. A.

“…Polymer products containing methoxycarbonyl-substituted cyclopropane groups in macromolecules with degrees of functionalization up to 40% have been obtained…”
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NMR for Determining the Structure of New Polysulfones by Gorbunova, M., Vorob'eva, A., Muslukhov, R.

“…The reactivity of N-allylated monomers of new structural types-N, N-diallyl-N′-acylhydrazines, 2,2-diallyl-1,1,3,3-tetraethylguanidiniumchloride, and…”
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Thiylation of (R)-4-Menthen-3-one and Its Derivatives by Ishmuratov, G. Yu, Tukhvatshin, V. S, Muslukhov, R. R, Yakovleva, M. P, Allagulova, A. V, Latypova, E. R, Talipov, R. F

“…Thiylation of (R)-4-menthen-3-one and its derivatives was studied. New sulfides and sulfoxides of the menthane series were synthesized…”
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Hydrochlorinated derivatives of syndiotactic 1,2-polybutadiene by Glazyrin, A. B., Abdullin, M. I., Muslukhov, R. R., Kraikin, V. A.

“…Chlorine-containing polymeric products with a degree of functionalization of up to 70% are synthesized through the hydrochlorination of syndiotactic…”
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Low-temperature hydride reduction of (3R)-carvomentholactone by Ishmuratov, G. Yu, Vydrina, V. A, Yakovleva, M. P, Galkina, Yu. A, Muslukhov, R. R, Tolstikov, G. A

“…Low-temperature (–70°C) reduction of (3R)-carvomentholactone by diisobutylaluminum hydride in methylenechloride was studied…”
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Chlorinated polymers based on low-molecular-mass 1,2-polybutadiene by Abdullin, M. I., Glazyrin, A. B., Asfandiyarov, R. N., Muslukhov, R. R.

“…It has been shown that chlorinated polymer products based on low-molecular-mass 1,2-polybuta-diene can be produced by incorporation of chlorine and hydrogen…”
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2-[(Diallyl)hydroxymethyl]pyrrolidine in radical (co)polymerization reactions by Kolesov, S. V., Vorob’eva, A. I., Gorbunova, M. N., Muslukhov, R. R., Tolstikov, A. G.

“…The feasibility of the free-radical (co)polymerization of 2-[(diallyl)hydroxymethyl]pyrrolidine is studied. It is found that, under radical-initiation…”
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(R)-4-menthen-3-one in the synthesis of (3S)-methylundecand (2S)-methyldec-1-ylbromides, key synthons for (S,S,S)-diprionylacetate by Latypova, E. R, Bannova, A. V, Muslukhov, R. R, Shutova, M. A, Talipov, R. F, Ishmuratov, G. Yu

“…New capabilities for the synthetic use of (R)-4-menthen-3-one were demonstrated using as examples (3S)-methylundec- and (2S)-methyldec-1-ylbromides, key…”
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Synthesis of symmetric macrocyclic diesterdihyrazides using successive [2+1]- and [1+1]-condensations by Ishmuratov, G. Yu, Mingaleeva, G. R, Yakovleva, M. P, Muslukhov, R. R, Vyrypaev, E. M, Ivanov, S. P, Tolstikov, A. G

“…Potentially useful symmetric macrocyclic diesterdihydrazides were synthesized efficiently from available petrochemical products (tetrahydropyran and…”
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Synthesis of macrolides with N-containing (azine or hydrazide) groups by Ishmuratov, G. Yu, Yakovleva, M. P, Mingaleeva, G. R, Muslukhov, R. R, Vyrypaev, E. M, Galkin, E. G, Ivanov, S. P, Tolstikov, A. G

“…Potentially useful 17-, and 22÷25-membered macrolides containing azine or hydrazide groups were synthesized from tetrahydropyran via [1+1]-condensation at room…”
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Synthesis of Optically Pure 3R-methylcyclopentan-1-one from L-(-)-menthol by Ishmuratov, G. Yu, Yakovleva, M. P., Ganieva, V. A., Gareeva, G. R., Muslukhov, R. R., Tolstikov, G. A.

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Synthesis from L-menthol of optically active macrolides with N-containing (azine or hydrazide) groups by Ishmuratov, G. Yu, Mingaleeva, G. R, Yakovleva, M. P, Muslukhov, R. R, Vyrypaev, E. M, Galkin, E. G, Tolstikov, A. G

“…Potentially useful 15- and 20-membered macrolides containing azine or hydrazide groups were synthesized from L-menthol via [1+1]-condensation at room…”
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Novel synthesis of (4R)-4-methylpentanolide from (L)-(−)-menthol by Ishmuratov, G. Yu, Yakovleva, M. P., Zaripova, G. V., Botsman, L. P., Muslukhov, R. R., Tolstikov, G. A.

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Prilezhaev dihydroxylation of (R)-octadec-9Z-en-7-0l by Muslukhov, R. R, Shayakhmetova, A. Kh, Shakhanova, O. O, Yakovleva, M. P, Ishmuratov, G. Yu, Tolstikov, A. G

“…Formation of new asymmetric centers with primarily the (S)-configuration was induced by the optically active center of (R)-octadec-9Z-en-7-ol upon Prilezhaev…”
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