A Hetero Diels-Alder Concerted Vs. Aldol Stepwise Mechanism In The Cyclization Of Silyloxyazadienes With Aldehydes: A Theoretical Study. (Articolo in rivista)

Type
Label
  • A Hetero Diels-Alder Concerted Vs. Aldol Stepwise Mechanism In The Cyclization Of Silyloxyazadienes With Aldehydes: A Theoretical Study. (Articolo in rivista) (literal)
Anno
  • 2006-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/ejoc.200500611 (literal)
Alternative label
  • Bongini A, Panunzio M. (2006)
    A Hetero Diels-Alder Concerted Vs. Aldol Stepwise Mechanism In The Cyclization Of Silyloxyazadienes With Aldehydes: A Theoretical Study.
    in European journal of organic chemistry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Bongini A, Panunzio M. (literal)
Pagina inizio
  • 972 (literal)
Pagina fine
  • 977 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 4 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 6 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • ISOF-CNR Dip. Ciamician, Unibo (literal)
Titolo
  • A Hetero Diels-Alder Concerted Vs. Aldol Stepwise Mechanism In The Cyclization Of Silyloxyazadienes With Aldehydes: A Theoretical Study. (literal)
Abstract
  • The Diels-Alder reaction of 3-silyloxy-2-azadiene with formaldehyde has been studied at the B3LYP/6-31G* level of theory and the role played by a Lewis acid evaluated. It is shown that the reaction is preferred when the Lewis acid coordinates to the aldehyde oxygen. This coordination allows for a concerted as well as a stepwise mechanism for the cyclization (literal)
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