Author:
Prestat Guillaume,Marchand Anne,Lebreton Jacques,Guingant André,Pradère Jean-Paul
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference7 articles.
1. Marchand, A.; Mauger, D.; Guingant, A.; Pradère, J. P. Tetrahedron: Asymmetry, 1995, 6, 853–856.
2. Previous examples of the use of carboxylic acids as chiral solvating agents for amines and amino alcohols can be found in the following review: Parker, D. Chem. Rev. 1991, 91, 1441–1457.
3. Previous use of carboxylic acids as CSAs for the determination of enantiomeric excess of chiral α-amino esters (three examples) and γ-amino ester (one example) by NMR spectroscopy, see: Benson, S. C.; Cai, P.; Colon, M.; Haiza, M. A.; Tokles, M.; Snyder, J. K. J. Org. Chem. 1988, 53, 5335–5341. Shapiro, M. J.; Archinal, A. E.; Jarema, M. A. J. Org. Chem. 1989, 54, 5826–5828.
4. All of these heterocycles were obtained following a hetero Diels–Alder protocol. Details of their preparation will be reported in a forthcoming full paper.
5. The superiority of OAc mandelic acid compared to mandelic acid or MTPA as a CSA was first pointed out by Parker et al. for a series of β-amino alcohols: Parker, D.; Taylor, R. J. Tetrahedron, 1987, 43, 5451–5456.
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