Synthesis of enantiopure aminonaphthol derivatives under conventional/ultrasonic technique and their ring-closure reaction


Pelit E., TURGUT Z.

ARABIAN JOURNAL OF CHEMISTRY, cilt.9, sa.3, ss.421-429, 2016 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 9 Sayı: 3
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1016/j.arabjc.2014.02.017
  • Dergi Adı: ARABIAN JOURNAL OF CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.421-429
  • Yıldız Teknik Üniversitesi Adresli: Evet

Özet

New optically active aminoalkylnaphthols were obtained by condensation of 2-naphthol, substituted aromatic and heteroaromatic aldehydes and (R)-(+)-1-phenylethylamine or (S)-(-)-1-phenylethylamine under conventional methods and ultrasonic irradiation. The enantiopure aminoalkylnaphthol derivatives were converted in ring-closure reaction with formaldehyde to the corresponding naphthoxazine derivatives. (C) 2014 King Saud University. Production and hosting by Elsevier B.V. All rights reserved.