Search Results - "Kulinkovich, O. G."

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    Titanacyclopropanes as versatile intermediates for carbon-carbon bond formation in reactions with unsaturated compounds by Kulinkovich, O. G.

    Published in Pure and applied chemistry (01-01-2000)
    “…Dialkoxytitanacyclopropane intermediates [or titanium (II)-olefin complexes] generated in situ from ethylmagnesium bromide and titanium (IV) isopropoxide react…”
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    Journal Article
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    1,n-Dicarbanionic Titanium Intermediates from Monocarbanionic Organometallics and Their Application in Organic Synthesis by Kulinkovich, Oleg G, de Meijere, Armin

    Published in Chemical reviews (09-08-2000)
    “…Kulinkovich and de Meijere compile the contributions to organic chemistry mainly made in the last 10-20 years, several of which have led to synthetically…”
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  3. 3

    Preparation of 3-bromomethyl-3-butenal diethylacetal and its conversion into isoprenoid aldehydes derivatives by Mineeva, I. V, Kulinkovich, O. G

    Published in Russian journal of organic chemistry (01-11-2009)
    “…The cyclopropanation of ethyl 3,3-diethoxypropionate with alkoxytitanacyclopropane reagents followed by the cleavage of the three-membered carbocycle in the…”
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    Synthesis of (+)-disparlure from diethyl (−)-malate via opening and fragmentation of the three-membered ring in tertiary cyclopropanols by Kovalenko, V. N, Masalov, N. V, Kulinkovich, O. G

    Published in Russian journal of organic chemistry (01-09-2009)
    “…(+)-Disparlure [(7R,8S)-7,8-epoxy-2-methyloctadecane, pheromone of the gypsy moth Lymantria dispar L.] was synthesized starting from diethyl (−)-malate via…”
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    Synthesis of epothilones molecule fragment (15R)-C ¹³ -C ²¹ from D-mannitol by Kovalenko, V. N, Sokolov, N. A, Kulinkovich, O. G

    Published in Russian journal of organic chemistry (01-11-2010)
    “…Efficient synthesis of an epothilone molecules fragment (15R)-C¹³-C²¹ was carried out from D-mannitol through its conversion into methyl…”
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    Stereoselective synthesis of cis-2-aryl- and 2-alkyl-1-chlorocyclopropanecarboxaldehydes by Verniest, Guido, Bombeke, Filip, Kulinkovich, O.G, De Kimpe, Norbert

    Published in Tetrahedron letters (01-01-2002)
    “…The title compounds were stereoselectively synthesized via a semi-benzilic Favorskii rearrangement of 3-aryl- and 3-alkyl-2,2-dichlorocyclobutanols, obtained…”
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    Synthesis of epothilone D with the forced application of oxycyclopropane intermediates by Hurski, A. L., Kulinkovich, O. G.

    Published in Russian journal of organic chemistry (01-11-2011)
    “…The total synthesis of epothilone D with six-fold application in the intermediate stages of successive cyclopropanation — opening or cleavage of the…”
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    The Chemistry of Cyclopropanols by Kulinkovich, Oleg G

    Published in Chemical reviews (01-07-2003)
    “…The present review is written for the purpose of reflecting recent achievements in the areas of synthesis and synthetic applications of cyclopropanols…”
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    Journal Article
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    Synthesis of methyl 3-bromomethylbut-3-enoate and its reactions with aldehydes and tributylchlorostannane in the presence of zinc by Mineeva, I. V., Kulinkovich, O. G.

    Published in Russian journal of organic chemistry (01-09-2008)
    “…Methyl 3-bromomethylbut-3-enoate smoothly reacted with prenal, β-ionylideneacetaldehyde, benzyloxyacetaldehyde, and tributylchlorostannane in the presence of…”
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  13. 13

    Synthesis of epothilones molecule fragment (15R)-C13-C21 from D-mannitol by Kovalenko, V. N., Sokolov, N. A., Kulinkovich, O. G.

    “…Efficient synthesis of an epothilone molecules fragment (15 R )-C 13 -C 21 was carried out from D-mannitol through its conversion into methyl 2,3- O…”
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    Differentiation between the ethoxycarbonyl groups in diethyl malate via their titanium-catalyzed reductive cyclopropanation with ethylmagnesium bromide and subsequent site-selective three-carbon ring cleavage by Bekish, Andrei V., Kulinkovich, Oleg G.

    Published in Tetrahedron letters (10-10-2005)
    “…Ethoxycarbonyl groups in O-THP protected racemic diethyl malate 1 were differentiated by their reductive cyclopropanation with ethylmagnesium bromide in the…”
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    A cyclopropanol approach to the synthesis of the C13–C21 fragment of epothilones from diethyl (S)-malate by Bekish, Andrei V., Isakov, Vladimir E., Kulinkovich, Oleg G.

    Published in Tetrahedron letters (10-10-2005)
    “…A convenient new approach to the synthesis of the C13–C21 epothilone fragment using the cyclopropanation of the ethoxycarbonyl groups in O-THP protected…”
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