Synthesis of haloconduritols from an endo-cycloadduct of furan and vinylene carbonate

BARAN A., Kazaz C., Secen H., SUTBEYAZ Y.

TETRAHEDRON, cilt.59, sa.20, ss.3643-3648, 2003 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 59 Sayı: 20
  • Basım Tarihi: 2003
  • Doi Numarası: 10.1016/s0040-4020(03)00510-6
  • Dergi Adı: TETRAHEDRON
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.3643-3648
  • Anahtar Kelimeler: haloconduritol, furan, vinylene carbonate, cycloaddition, ring-opening, boron trihalides, neighboring group participation, trans-esterification, STEREOSPECIFIC SYNTHESIS, BROMOCONDURITOL, DERIVATIVES, INHIBITORS, CONDURITOLS
  • Atatürk Üniversitesi Adresli: Evet

Özet

A method for preparing haloconduritols having a conduritol-A construction is described. A mixture of endo- and exo-cycloadduct derivatives prepared from the Diels-Alder reaction of furan and vinylene carbonate was converted into diacetate derivatives by hydrolysis (K2CO3/MeOH) followed by acetylation (Ac2O/Pyridine). Boron trihalide (BBr3 or BCl3)-assisted ring-opening of the endo-diacetate in CH2O2 at -78degreesC gave (1alpha,2alpha,30,6beta)-6-halogeno-4-cyclohexene-1,2,3-triol 1,2-diacetate from which the corresponding triacetate was prepared by acetylation (AcCl). trans-Esterification of the triacetate (MeOH/HCl) afforded (1alpha,2alpha,3beta,6beta)-6-halogeno-4-cyclohexene-1,2,3-triol (X=Br or Cl). BF3-Assisted ring-opening of the endo-diacetate in CH2O2 gave (1alpha,2alpha,3beta,6beta)-6-chloro-4-cyclohexene-1,2,3-triol 1,2-diacetate by means of halogen exchange. (C) 2003 Elsevier Science Ltd. All rights reserved.