Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List D(-)-Norvaline

D(-)-Norvaline synthesis

6synthesis methods
-

Yield: 88 % ee

Reaction Conditions:

with isopropylamine in aq. buffer; pH=7.0 for 48 h;Enzymatic reaction;Overall yield = 90 %;Time;

Steps:

2.7 Preparative-Scale Deracemization
General procedure: Deracemization of dl-1a in a preparative-scale was carried out in a 25 mL reaction mixture (50 mM Tris buffer, pH 7.0)charged with 0.22 g dl-1a (2.5 mmol), 0.15 g 3 (2.5 mmol),17 mg NAD+,1750 U AlaDH, 40 U ARTAmut and 250 U NOX. Reaction was carried under magnetic stirring at 37 °C.Aliquots (typically 10 μL) of the reaction mixture were takenat predetermined reaction time and mixed with 40 μL of 5 NHCl after 20-fold dilution with water. Quantitative chiral analysis of dl-1a was performed by HPLC for determination of eeD. When eeD of d-1a exceeded 99%, reaction was stopped and then product isolation was performed. The pH of the reaction mixture was adjusted to 1.0 byadding 5 N HCl and then filtered using a glass-fritted filter funnel to remove protein precipitates. The filtrate was loaded on a glass column packed with Dowex 50WX8 cation exchange resin (40 g), followed by washing with 0.1 N HCl(100 mL) and then water (50 mL). Elution was performed by 10% (v/v) aqueous ammonia solution (150 mL) and then the eluate was evaporated at 70 °C and 0.25 bar. The resulting white solid was washed with ethanol (20 mL) and dried overnight at 37 °C.

References:

Han, Sang-Woo;Shin, Jong-Shik [Catalysis Letters,2018,vol. 148,# 12,p. 3678 - 3684]

D(-)-Norvaline Related Search: