Enantioselective synthesis of 4,5,6,7-tetrahydro-4-oxo-benzofuran-5-yl acetate and 1-benzyl-4,5,6,7-tetrahydro-4-oxo-1(H)-indol-5-yl acetate using chemoenzymatic methods

Demir, Ayhan; Caliskan, Zerrin; Sahin, Ertan

doi:10.1016/j.molcatb.2006.09.006

Enantioselective synthesis of 4,5,6,7-tetrahydro-4-oxo-benzofuran-5-yl acetate and 1-benzyl-4,5,6,7-tetrahydro-4-oxo-1(H)-indol-5-yl acetate using chemoenzymatic methods

Atıf İçin Kopyala

Demir A. S., Caliskan Z., Sahin E.

JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, cilt.44, ss.87-92, 2007 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 44
Basım Tarihi: 2007
Doi Numarası: 10.1016/j.molcatb.2006.09.006
Dergi Adı: JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.87-92
Atatürk Üniversitesi Adresli: Evet

Özet

The chemoenzymatic synthesis of both of the enantiomers of pharmacologically interesting compounds such as 4,5,6,7-tetrahydro-4-oxobenzofuran-5-yl acetate (2a), 4,5,6,7-tetrahydro-4-oxo-6,6-dimethylbenzofuran-5-yl acetate (2b), and their hydroxy derivatives 3a, 3b, 1-benzyl4,5,6,7-tetrahydro-4-oxo-1(H)-indol-5-yl acetate (5), starting from 6,7-dihydrobenzofuran-4(5H)-one (la), 6,7-dihydro-6,6-dimethylbenzofuran4(5H)-one (7b), and 1-benzyl-6,7-dihydro-1 H-indol-4(5H)-one (4) are reported. Manganese(III) acetate-mediated acetoxylation followed by the enzyme-mediated kinetic resolution of alpha'-acetoxy enone provides acetoxy and hydroxy derivatives in good yields and high enantiomeric excesses. (c) 2006 Elsevier B.V. All rights reserved.