BUTENOLIDE ANNELATIONS USING A MANGANESE(III) OXIDATION - A SYNTHESIS OF JOLKINOLIDE-E

DEMIR A., TANYELI C., AKGUN H., CALISKAN Z., OZGUL E.

BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE, cilt.132, sa.4, ss.423-427, 1995 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 132 Sayı: 4
  • Basım Tarihi: 1995
  • Dergi Adı: BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.423-427
  • Anahtar Kelimeler: (-)-JOLKINOLIDE E, MANGANESE(III) ACETATE OXIDATION, BUTENOLIDE ANNELATION, CARBOXYLIC-ACIDS, ACETATE, COMBINATION, KETONES
  • Orta Doğu Teknik Üniversitesi Adresli: Evet

Özet

A general procedure was developed for the annelation of a butenolide to an enone that highlighted a manganese(III) oxidation of an enone. The merit of this procedure was illustrated in a synthesis of (-)-jolkinolide E, ent-1, from (+)-manool 11. A potassium permanganate-mediated degradation of 11 and dehydration of an intermediate beta-hydroxyketone 12 according to a literature procedure afforded a tricyclic enone 13. Oxidation of 13 with manganese(III) acetate and chloropropionic acid regio- and stereoselectively furnished a C-12 alpha chloropropionyl ester 14. An Arbuzov reaction of 14 with triethylphosphite and an intramolecular Horner-Emmons cyclization of the resulting phosphonate 15 gave (-)-jolkinolide E, the structure of which was investigated in detail by NMR. This methodology was also applied to 4,4-dimethylcyclohex-2-en-1-one. This overall approach offers a general solution to the problem of butenolide annelation to enones.