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      <dc:title>Cp2TiCl-catalyzed highly stereoselective intramolecular epoxide allylation using allyl carbonates</dc:title>
      <dc:creator>Rodríguez Márquez, Irene</dc:creator>
      <dc:creator>Milán Delgado, Alba</dc:creator>
      <dc:creator>González Campaña, Araceli</dc:creator>
      <dc:creator>Cuerva Carvajal, Juan Manuel</dc:creator>
      <dc:subject>Intramolecular epoxide allylation</dc:subject>
      <dc:subject>Allyl carbonates</dc:subject>
      <dc:subject>Diastereoselective synthesis</dc:subject>
      <dc:description>A useful method for the diastereoselective synthesis of vinyl substituted carbo- and heterocycles is described. Highly functionalized structures difficult to achieve by other methodologies are obtained in a single step by this procedure.</dc:description>
      <dc:date>2017-07-28T10:19:05Z</dc:date>
      <dc:date>2017-07-28T10:19:05Z</dc:date>
      <dc:date>2014-01-14</dc:date>
      <dc:type>info:eu-repo/semantics/article</dc:type>
      <dc:identifier>Rodríguez Márquez, I.; et al. Cp2TiCl-catalyzed highly stereoselective intramolecular epoxide allylation using allyl carbonates. Organic Chemistry Frontiers, 4: 373-381 (2014). [http://hdl.handle.net/10481/47294]</dc:identifier>
      <dc:identifier>2052-4129</dc:identifier>
      <dc:identifier>2052-4110</dc:identifier>
      <dc:identifier>http://hdl.handle.net/10481/47294</dc:identifier>
      <dc:identifier>10.1039/C4QO00012A</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/</dc:rights>
      <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
      <dc:rights>Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License</dc:rights>
      <dc:publisher>Royal Society of Chemistry</dc:publisher>
   </ow:Publication>
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