Optical Resolution by Preferential Crystallization and Replacing Crystallization of DL-Allothreonine
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/67/7/67_7_1899/_pdf
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3. Cleavage of Epoxide Ring of Glycidic Acids with Ammonia. I-II. I. Formation of Hydroxyvaline and β-Amino-α hydroxyisovaleric Acid from ft, β-Dimethylglycidic Acid
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1. Solubility Equilibria and Crystallographic Characterization of the l-Threonine/l-allo-Threonine System, Part 1: Solubility Equilibria in the Threonine Diastereomeric System;Crystal Growth & Design;2013-12-18
2. An Efficient Route to Both Enantiomers of allo-Threonine by Simultaneous Amino Acid Racemase-Catalyzed Isomerization of Threonine and Crystallization;Advanced Synthesis & Catalysis;2011-05-23
3. Preparation of Optically Active Allothreonine via Optical Resolution by Replacing Crystallization.;Chemical and Pharmaceutical Bulletin;2002
4. Influence of the Process on the Mechanisms and the Performances of the Preferential Crystallization: Example with (±)-5-(4-Bromophenyl)-5-methylhydantoin;Chemistry Letters;2001-04
5. Optical Resolution by Preferential Crystallization of (RS)-2-Amino-3-(2-carboxyethylthio)propanoic Acid;Bioscience, Biotechnology, and Biochemistry;1998-01
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