Electrophilic ring opening of oxazolines derived from serine and threonine: A practical entry to N(N)-protected β-halogeno α-aminoesters

Author:

Laaziri Abdelhamid,Uziel Jacques,Jugé Sylvain

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference44 articles.

1. For some reviews on oxazolines see: (a) Frump, J. A. Chem. Rev. 1971, 71, 483–505.

2. (b) Gant, T. G.; Meyers A. I. Tetrahedron 1994, 50, 2297–2360.

3. Goethals, E. J. In Comprehensive Polymer Science, Vol. 3, Allen, G.; Bevington, J. C. Eds, Pergamon Press, Oxford, 1989, pp. 837–866.

4. (a) Brunner, H.; Zettlmeier, W. Handbook of Enantioselective Catalysis, Vol. 2, VCH, Basel, 1993.

5. For typical efficient chiral oxazolines ligands see: (b) Allen, J. V.; Williams, J. M. J. Tetrahedron: Asymmetry 1994, 5, 277–282.

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