Enantioselective Routes to Sulfoxides Based Upon the Use of Carbanionic Leaving Groups (Articolo in rivista)

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  • Enantioselective Routes to Sulfoxides Based Upon the Use of Carbanionic Leaving Groups (Articolo in rivista) (literal)
Anno
  • 2004-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/ejoc.2003.00497 (literal)
Alternative label
  • Capozzi M.A.M., Cardellicchio C., Naso F. (2004)
    Enantioselective Routes to Sulfoxides Based Upon the Use of Carbanionic Leaving Groups
    in European journal of organic chemistry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Capozzi M.A.M., Cardellicchio C., Naso F. (literal)
Pagina inizio
  • 1855 (literal)
Pagina fine
  • 1863 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • CNR ICCOM (literal)
Titolo
  • Enantioselective Routes to Sulfoxides Based Upon the Use of Carbanionic Leaving Groups (literal)
Abstract
  • Several carbanionic leaving groups can be easily displaced from the sulfinyl group by organometallic reagents. The reaction follows a highly stereoselective course of inversion of configuration. Provided that a ready route to the precursor sulfinyl compound is available (e.g. an enantioselective ox-idation of the corresponding sulfide), the process can be transformed into an easy and versatile procedure for the ster-eoselective synthesis of sulfoxides. (literal)
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