Allylation and heterocycloaddition reactions of aldimines: Furan- and quinolinecarboxaldehydes


Kouznetsov V., Ocal N., Turgut Z. , Zubkov F., Kaban S., Varlamov A.

MONATSHEFTE FUR CHEMIE, vol.129, pp.671-677, 1998 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 129
  • Publication Date: 1998
  • Doi Number: 10.1007/s007060050087
  • Journal Name: MONATSHEFTE FUR CHEMIE
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.671-677

Abstract

New derivatives of alpha-substituted furans were prepared in high yields from easily available alpha-furfurylidenbenzilamines via nucleophilic C-allylation. The homoallylamines obtained this way were used for the synthesis of some polyfunctional aminobutene derivatives. In addition, 4-thiazolidinones some of which are hetaryl substituted at the 2-position were prepared by the reaction of mercapto acids with quinoline carboxaldehydes and p-phenetidine. All new products were fully characterized.