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Multigram Synthesis of Advanced 6,6-Difluorospiro[3.3]heptane-derived Building Blocks.
Olifir, Oleksandr S; Chernykh, Anton V; Dobrydnev, Alexey V; Grygorenko, Oleksandr O; Moroz, Yuriy S; Voitenko, Zoia V; Radchenko, Dmytro S.
Afiliación
  • Olifir OS; Enamine Ltd. (www.enamine.net), Chervonotkatska Street 78, Kyiv 02094, Ukraine.
  • Chernykh AV; Taras Shevchenko National University of Kyiv, Volodymyrska Street 60, Kyiv 01601, Ukraine.
  • Dobrydnev AV; Enamine Ltd. (www.enamine.net), Chervonotkatska Street 78, Kyiv 02094, Ukraine.
  • Grygorenko OO; Enamine Ltd. (www.enamine.net), Chervonotkatska Street 78, Kyiv 02094, Ukraine.
  • Moroz YS; Taras Shevchenko National University of Kyiv, Volodymyrska Street 60, Kyiv 01601, Ukraine.
  • Voitenko ZV; Enamine Ltd. (www.enamine.net), Chervonotkatska Street 78, Kyiv 02094, Ukraine.
  • Radchenko DS; Taras Shevchenko National University of Kyiv, Volodymyrska Street 60, Kyiv 01601, Ukraine.
European J Org Chem ; 2021(47): 6541-6550, 2021 Dec 21.
Article en En | MEDLINE | ID: mdl-35095338
A convenient methodology for constructing 6,6-difluorospiro[3.3]heptane scaffold - a conformationally restricted isostere of gem-difluorocycloalkanes - is developed. Alarge array of novel 2-mono- and 2,2-bifunctionalized difluorospiro[3.3]heptane building blocks was obtained through the convergent synthesis strategy using a common synthetic precursor - 1,1-bis(bromomethyl)-3,3-difluorocyclobutane. The target compounds and intermediates were prepared by short reaction sequences (6-10 steps) on multigram scale (up to 0.47 kg).
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: European J Org Chem Año: 2021 Tipo del documento: Article País de afiliación: Ucrania

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: European J Org Chem Año: 2021 Tipo del documento: Article País de afiliación: Ucrania