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Remarkably facile hexatriene electrocyclizations as a route to functionalized cyclohexenones via ring expansion of cyclobutenones.
Magomedov, Nabi A; Ruggiero, Piero L; Tang, Yuchen.
Affiliation
  • Magomedov NA; Department of Chemistry, University of Rochester, Rochester, NY 14627-0216, USA. magomedov@chem.rochester.edu
J Am Chem Soc ; 126(6): 1624-5, 2004 Feb 18.
Article de En | MEDLINE | ID: mdl-14871080
ABSTRACT
This Communication describes a cascade reaction sequence that leads to highly functionalized cyclohexenones starting from reaction of cyclobutenones with alpha-lithio-alpha,beta-unsaturated sulfones and amides. The hexatriene-cyclohexadiene cyclization steps presumed to be involved in these transformations are among the most facile hexatriene electrocyclizations reported thus far.
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Am Chem Soc Année: 2004 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Am Chem Soc Année: 2004 Type de document: Article Pays d'affiliation: États-Unis d'Amérique