Majewski, M. and Nowak, P. (1999) Stereoselective Synthesis of Protected Ketohexoses via Aldol Reaction of Chiral Dioxanone Enolate. Synlett, 9, 1447-1449. http://dx.doi.org/10.1055/s-1999-2862
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-1999-2862

has been cited by the following article:

• TITLE: Stereoselective Aldol Reaction in Aqueous Solution Using Prolinamido-Glycosides as Water-Compatible Organocatalyst

  AUTHORS: Daisuke Miura, Tomoya Machinami

  KEYWORDS: Organocatalyst, Aldol Reaction, Carbohydrate, Water-Compatible, Prolinamide

  JOURNAL NAME: Modern Research in Catalysis, Vol.4 No.1, January 9, 2015

  ABSTRACT: Prolinamido-glycoside catalyzed asymmetric aldol reaction in aqueous media is reported. The reactions are rapid and highly stereoselective when water is used as solvent. The stereoselectivities were under influence of configurations of a prolyl residue of the catalyst and α-chiral aldehydes. Water soluble prolinamido-glycoside catalysts are easily separable from reaction mixture and can be recycled and re-used several times.