Chemistry Letters p. 553 - 556 (1993)
Update date:2022-08-17
Topics:
Kikuchi, Jun-ichi
Takashima, Toru
Nakao, Hidetoshi
Hie, Ken-ichi
Etoh, Hiroshi
et al.
The aldolation of glycine with benzaldehyde to yield β-phenylserine was catalyzed by supramolecular assemblies formed with a synthetic peptide lipid, a hydrophobic vitamin B6 derivative, and zinc(II) ions in aqueous media under mild conditions.A diastereomeric ratio of the reaction products was much dependent on a size and a phase property of the vesicular catalyst.
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