Selective monoacetylation of diol compounds by Aspergillus niger lipase | Zendy

KwoFeng Hsiao | Zendy; FangLin Yang | Zendy; ShihHsiung Wu | Zendy; KungTsung Wang | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Open Access

Selective monoacetylation of diol compounds by Aspergillus niger lipase

Author(s) -

KwoFeng Hsiao,

FangLin Yang,

ShihHsiung Wu,

KungTsung Wang

Publication year - 1996

Publication title -

biotechnology letters

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.548

H-Index - 107

eISSN - 1573-6776

pISSN - 0141-5492

DOI - 10.1007/bf00129954

Subject(s) - aspergillus niger , lipase , diol , regioselectivity , chemistry , vinyl acetate , thio , alcohol , triacylglycerol lipase , organic chemistry , aspergillus , propanediol , stereochemistry , enzyme , catalysis , biochemistry , biology , microbiology and biotechnology , polymer , copolymer

The primary monoesters of diol compounds were formed exclusively in the reaction with vinyl acetate and Aspergillus niger lipase for 24~72 h. Various diol compounds which included 1,3-butanediol, 1,4-butanediol, 1,5-hexanediol, 1-phenyl-1,2-ethanediol, 1-phenyl-1,3-propanediol, 2, 3, or 4-hydroxybenzyl alcohol, methyl 2, 3-O-acetyl-D-glycopyranosides and phenyl 1-thio-ß-D-xylopyranoside have been examined and showed nearly 100% regioselectivity.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.

Having issues? You can contact us here

Accelerating Research