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  <title>Unitus DSpace</title>
  <link rel="alternate" href="http://http://dspace.unitus.it:80" />
  <subtitle>The DSpace digital repository system captures, stores, indexes, preserves, and distributes digital research material.</subtitle>
  <id>http://http://dspace.unitus.it:80</id>
  <updated>2013-05-24T15:12:42Z</updated>
  <dc:date>2013-05-24T15:12:42Z</dc:date>
  <entry>
    <title>An efficient and selective epoxidation of olefins with novel methyltrioxorhenium/(fluorous ponytailed) 2,2′-bipyridine catalysts</title>
    <link rel="alternate" href="http://hdl.handle.net/2067/1795" />
    <author>
      <name>Saladino, Raffaele</name>
    </author>
    <author>
      <name>Ginnasi, Maria Cristina</name>
    </author>
    <author>
      <name>Collalto, Daniela</name>
    </author>
    <author>
      <name>Bernini, Roberta</name>
    </author>
    <author>
      <name>Crestini, Claudia</name>
    </author>
    <id>http://hdl.handle.net/2067/1795</id>
    <updated>2011-06-29T15:42:40Z</updated>
    <published>2009-12-31T23:00:00Z</published>
    <summary type="text">Title: An efficient and selective epoxidation of olefins with novel methyltrioxorhenium/(fluorous ponytailed) 2,2′-bipyridine catalysts
Authors: Saladino, Raffaele; Ginnasi, Maria Cristina; Collalto, Daniela; Bernini, Roberta; Crestini, Claudia
Abstract: Novel complexes between methyltrioxorhenium (MTO) and bis(fluorous- ponytailed) 2,2′bipyridines (bpy-Fn) were synthesized and used for the oxidation of alkenes with hydrogen peroxide under fluorous catalysis. High conversions and yields of the corresponding epoxides were obtained.
Description: L'articolo è disponibile sul sito dell'editore: http://www.onlinelibrary.wiley.com</summary>
    <dc:date>2009-12-31T23:00:00Z</dc:date>
  </entry>
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