Author/Authors :
Wilke، نويسنده , , Burkhardt I. and Goodenough، نويسنده , , Angela K. and Bausch، نويسنده , , Cory C. and Cline، نويسنده , , Erika N. and Leigh Abrams، نويسنده , , M. and Fayer، نويسنده , , Effrat L. and Cermak، نويسنده , , Diana M.، نويسنده ,
Abstract :
Derivatives of camphorsultam which contain novel spirooxazolidine and spirooxazine structures have been prepared in high yield and purity. Though it was expected that the ketone moiety would undergo acetal formation, the imine instead underwent reaction and was proven by X-ray crystallography and 2D NMR techniques. The initial ketone-containing derivatives were then reduced to produce exo-hydroxy analogs that have potential as a new family of chiral auxiliaries.
Keywords :
Camphor , asymmetric synthesis , acetal formation , Strained ring systems