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Organocatalytic Enantioselective Cross-Aldol Reaction of o-Hydroxyarylketones and Trifluoromethyl Ketones.
Wang, Pei; Li, Hong-Feng; Zhao, Jia-Zhen; Du, Zhi-Hong; Da, Chao-Shan.
Afiliación
  • Wang P; Institute of Biochemistry and Molecular Biology, School of Life Sciences, Lanzhou University , Lanzhou 730000, China.
  • Li HF; Institute of Biochemistry and Molecular Biology, School of Life Sciences, Lanzhou University , Lanzhou 730000, China.
  • Zhao JZ; Institute of Biochemistry and Molecular Biology, School of Life Sciences, Lanzhou University , Lanzhou 730000, China.
  • Du ZH; Institute of Biochemistry and Molecular Biology, School of Life Sciences, Lanzhou University , Lanzhou 730000, China.
  • Da CS; Institute of Biochemistry and Molecular Biology, School of Life Sciences, Lanzhou University , Lanzhou 730000, China.
Org Lett ; 19(10): 2634-2637, 2017 05 19.
Article en En | MEDLINE | ID: mdl-28481099
The enantioselective cross-aldol reaction between o-hydroxyacetophenones and trifluoromethyl ketones catalyzed by chiral thiourea organocatalysts is reported. Gram-scale synthesis of the cross-aldol product was carried out, with no decrease in the yield and enantioselectivity. Furthermore, the cross-aldol products thus prepared were used in the preparation of medicinally interesting 3,5-diaryl-5-trifluoromethyl-2-isoxazoline and ß-trifluoromethyl-ß-tertiary hydroxy acid ester with high yield and enantiopurity.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2017 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2017 Tipo del documento: Article País de afiliación: China