Study of a 1,6-hydride shift in an open chain of hydroxylactam-triarylcarbinols
Résumé
Hydroxylactam-alcohols 5a,b,d (isoindole series), under acidic treatment gave phthalimides 7a,b,d via a hydride shift induced by an intramolecular pi -stacking (benzene-benzene or benzene-thiophene interaction) which did not occur in 10a (succinimide series). (C) 2001 Elsevier Science Ltd. All rights reserved.
Origine | Fichiers produits par l'(les) auteur(s) |
---|
Loading...