Search Results - "Masalov, Nikolai"

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  1. 1

    Low-Valent Titanium-Mediated Cyclopropanation of Vinylogous Esters by Masalov, Nikolai, Feng, Wei, Cha, Jin Kun

    Published in Organic letters (08-07-2004)
    “…Inter- and intramolecular titanium-mediated cyclopropanation reactions of vinylogous esters are reported. Comparison between the Kulinkovich cyclopropanation…”
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    Journal Article
  2. 2

    Diastereoselective, Titanium-Mediated Cyclization of ω-Vinyl Tethered Imides by Santra, Soumava, Masalov, Nikolai, Epstein, Oleg L, Cha, Jin Kun

    Published in Organic letters (22-12-2005)
    “…Diastereoselective reductive coupling reactions of ω-vinyl tethered cyclic imides are achieved by a preexisting stereocenter at an allylic position…”
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    Journal Article
  3. 3

    Titanium-Mediated Alkylative Coupling of N-Acylpyrroles by Epstein, Oleg L, Seo, Jung Min, Masalov, Nikolai, Cha, Jin Kun

    Published in Organic letters (26-05-2005)
    “…Inter- and intramolecular titanium-mediated coupling reactions of N-acylpyrroles are reported for convenient functionalization of terminal olefins. Comparison…”
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  4. 4

    New synthetic route to the alkaloid withasomnine by ring transformation of a functionalized cyclopropanol via the parent pyrrolo[1,2-b]pyrazole by Kulinkovich, Oleg, Masalov, Nikolai, Tyvorskii, Vladimir, De Kimpe, Norbert, Keppens, Marian

    Published in Tetrahedron letters (12-02-1996)
    “…Withasomnine has been prepared by rearrangement of 1-(3-chloropropyl)-cyclopropanol into 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole, followed by bromination and…”
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  5. 5

    Enantioselective Synthesis of Functionalised Decalones by Robinson Annulation of Substituted Cyclohexanones, Derived from R-(−)-Carvone by Jansen, Ben J.M, Hendrikx, Cindy C.J, Masalov, Nikolai, Stork, Gerrit A, Meulemans, Tommi M, Macaev, Fliur Z, de Groot, Aede

    Published in Tetrahedron (31-03-2000)
    “…The copper catalysed conjugate addition of methyl magnesium iodide to cyclohexenones and trapping of the enolate as its trimethylsilyl enol ether, followed by…”
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