The catalysis and asymmetric induction of chiral reverse micelle: Synthesis of optically active α-amino acids

Article abstract of DOI:10.1080/00397919708005465

Through alkylation of N-benzylideneglycine ethyl ester in chiral reverse micelle, followed by hydrolysis of the resulting products, optically active α-amino acids were synthesized.

Full text of DOI:10.1080/00397919708005465

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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The Catalysis and Asymmetric
Induction of Chiral Reverse
Micelle: Synthesis of Optically
Active α-Amino Acids
Peipei Sun a & Yongmin Zhang a
a Department of Chemistry , Hangzhou University ,
Hangzhou, 310028, P. R. China
Published online: 22 Aug 2006.
To cite this article: Peipei Sun & Yongmin Zhang (1997) The Catalysis and Asymmetric
Induction of Chiral Reverse Micelle: Synthesis of Optically Active α-Amino Acids,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 27:23, 4173-4179, DOI: 10.1080/00397919708005465
To link to this article: http://dx.doi.org/10.1080/00397919708005465
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