Allylation and heterocycloaddition reactions of aldimines: Furan- and quinolinecarboxaldehydes

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

MONATSHEFTE FUR CHEMIE, cilt.129, ss.671-677, 1998 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 129
  • Basım Tarihi: 1998
  • Doi Numarası: 10.1007/s007060050087
  • Dergi Adı: MONATSHEFTE FUR CHEMIE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.671-677
  • Yıldız Teknik Üniversitesi Adresli: Evet

Özet

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.