Optical Resolution oferythro-2-Amino-1,2-diphenylethanol by Reciprocal Crystallization of the Diastereomeric Salts with (−)-Mandelic Acid on Alternate Seeding
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/59/9/59_9_2915/_pdf
Reference5 articles.
1. Optical Resolution of 2-Amino-1,2-diphenylethanol by Preferential Crystallization and Its Utilization in Fractional Crystallization and Enantioselective Reduction of Prochiral Ketones
2. Application of erythro-2-methoxy-1,2-diphenylethylamine to enantioselective alkylation of cyclohexanone
3. Preparation of the Stereoisomeric α,β-Diphenyl-β-hydroxyethylamines
4. Improved chiral derivatizing agents for the chromatographic resolution of racemic primary amines
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1. Gas Antisolvent Fractionation: a New Method to Obtain Enantiopure Compounds, a Case Study on Mandelic Acid;Periodica Polytechnica Chemical Engineering;2018-04-04
2. A Simple, Scalable Synthetic Route to (+)- and (−)-Pseudoephenamine;Organic Letters;2013-10-18
3. Solvent-Induced Reversed Stereoselectivity in Reciprocal Resolutions of Mandelic Acid and erythro-2-Amino-1,2-diphenylethanol;The Journal of Organic Chemistry;2013-09-04
4. An Improved Synthesis of Optically Pure 4-Boc-5,6-Diphenylmorpholin-2-one and 4-Cbz-5,6-Diphenylmorpholin-2-one;Synlett;2005
5. Reductive Coupling of Aldehydes with Nitriles Promoted by Titanium Tetraiodide;Letters in Organic Chemistry;2004-10-01
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