Design of resolving reagents: p-substituted mandelic acids as resolving reagents for 1-arylalkylamines
- 30 June 1996
- journal article
- research article
- Published by Elsevier BV in Tetrahedron: Asymmetry
- Vol. 7 (6), 1539-1542
- https://doi.org/10.1016/0957-4166(96)00175-9
Abstract
No abstract availableKeywords
Funding Information
- Japan Society for the Promotion of Science (06004310, 06242101, 07555581)
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 8 references indexed in Scilit:
- The chiral amino alcohol, cis-2-amino-1-acenaphthenol: Synthesis, resolution, and application to the diastereoselective [2,3]-Wittig rearrangementTetrahedron: Asymmetry, 1994
- Predictions of which diastereoisomeric salt precipitates during an optical resolution via diastereoisomeric salt formationTetrahedron, 1994
- Optical Resolution of 1-(3-Methoxyphenyl)ethylamine with Enantiomerically Pure Mandelic Acid, and the Crystal Structure of Less-Soluble Diastereomeric SaltBulletin of the Chemical Society of Japan, 1993
- Towards a rational design for resolving agents. Part V: Substituent effects in the resolution of ephedrine using a series of cyclic phosphoric acidsRecueil des Travaux Chimiques des Pays-Bas, 1993
- Resolution of Racemic Amines with 2-Methyl-2-phenylbutanedioic AcidSynthesis, 1988
- The design of resolving agents. Chiral cyclic phosphoric acidsThe Journal of Organic Chemistry, 1985
- Optical Resolution of 2-Amino-1,2-diphenylethanol by Preferential Crystallization and Its Utilization in Fractional Crystallization and Enantioselective Reduction of Prochiral KetonesBulletin of the Chemical Society of Japan, 1982
- Semisynthetic cephalosporins. Synthesis and structure-activity relations of 7-mandelamido-3-cephem-4-carboxylic acidsJournal of Medicinal Chemistry, 1974