Enzyme-assisted Preparation of D-tert.-Leucine(Organic Chemistry)
スポンサーリンク
概要
- 論文の詳細を見る
Optically pure n-tert. -leucine was obtained by the enzymatic hydrolysis of (±)-N-acetyl-tert. leucine chloroethyl ester after about 50% conversion, this being catalyzed by a protease from Bacillus licheniformis (Alcalase^[○!R]), and subsequent acidic saponification of the recovered ester. Among the methyl, ethyl, octyl, chloroethyl and trichloroethyl esters, the chloroethyl ester exhibited the highest rate of hydrolysis.
- 社団法人日本農芸化学会の論文
- 2001-09-23
著者
-
Auer Kurt
Novartis Pharma Ag Core Technology Area
-
Ghisalba Oreste
Novartis Pharma Ag
-
LAUMEN Kurt
Novartis Pharma AG, Core Technology Area
-
Laumen Kurt
Novartis Pharma Ag Core Technology Area
関連論文
- Preparation of 4-(4'-Hydroxyanilino)-5-anilinophthalimide and 4,5-Bis-(4'-hydroxyanilino)-phthalimide by microbial Hydroxylation
- Preparative 2'-Reduction of ATP Catalyzed by Ribonucleotide Reductase Purified by Liquid-Liquid Extraction
- Chemo-enzymatic Synthesis of both Enantiomers of myo-Inositol 1,3,4,5-tetrakisphosphate
- Enzyme-assisted Preparation of D-tert.-Leucine(Organic Chemistry)