Lithiation of N-Alkyl-(o-tolyl)aziridine: Stereoselective Synthesis of Isochromans (Articolo in rivista)

Type
Label
  • Lithiation of N-Alkyl-(o-tolyl)aziridine: Stereoselective Synthesis of Isochromans (Articolo in rivista) (literal)
Anno
  • 2009-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/jo9011943 (literal)
Alternative label
  • Dammacco M.; Degennaro L.; Florio S.; Luisi R.; Musio B.; Altomare A. (2009)
    Lithiation of N-Alkyl-(o-tolyl)aziridine: Stereoselective Synthesis of Isochromans
    in Journal of organic chemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Dammacco M.; Degennaro L.; Florio S.; Luisi R.; Musio B.; Altomare A. (literal)
Pagina inizio
  • 6319 (literal)
Pagina fine
  • 6322 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 74 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Dipartimento Farmaco-Chimico Università di Bari; CINMPIS Bari; Istituto di Cristallografia-CNR Sede di Bari (literal)
Titolo
  • Lithiation of N-Alkyl-(o-tolyl)aziridine: Stereoselective Synthesis of Isochromans (literal)
Abstract
  • The lithiation reaction of o-tolylaziridine 1 has been investigated by using the aziridine ring capability to act as a directing metalation group. Trapped with electrophiles, the resulting o-aziridinyl benzyllithium 1-Li elves access to several functionalized aziridines 2a-j. The hydroxyalkylated derivatives 2d-j were converted into important scaffolds such as isochromans 3a-d. A stereoselective preparation of isochromans (R)-3b, (1R,3S)-3d, and (1R,3R)-3d has been developed starting froth enantioenriched o-tolylaziridine. (literal)
Prodotto di
Autore CNR
Insieme di parole chiave

Incoming links:


Prodotto
Autore CNR di
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi
Insieme di parole chiave di
data.CNR.it