Lithium hydroxide as base in the Wittig reaction. A simple method for olefines synthesis (Articolo in rivista)

Type
Label
  • Lithium hydroxide as base in the Wittig reaction. A simple method for olefines synthesis (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tet.2008.02.091 (literal)
Alternative label
  • Antonioletti R., Bonadies F., Ciammaichella A., Veglianti A. (2007)
    Lithium hydroxide as base in the Wittig reaction. A simple method for olefines synthesis
    in Tetrahedron (Oxf., Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Antonioletti R., Bonadies F., Ciammaichella A., Veglianti A. (literal)
Pagina inizio
  • 4644 (literal)
Pagina fine
  • 4648 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 64 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 5 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 20 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Univ Roma La Sapienza, Dipartimento Chim, Ist Chim Biomol, CNR,Sez Roma, P A Moro 5, I-00185 Rome, Italy. (literal)
Titolo
  • Lithium hydroxide as base in the Wittig reaction. A simple method for olefines synthesis (literal)
Abstract
  • A mild and practical procedure for the Wittig olefination, promoted by lithium hydroxide and triphenylbenzyl phosphonium bromide, has been set up for the synthesis of stilbenes and styrenes. The experimental conditions allow aromatic, heteroaromatic, unsaturated and saturated aliphatic aldehydes to give final products in good yields. (literal)
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