Highly Stereoselective Recognition and Deracemization of Amino Acids by Supramolecular Self-Assembly

Authors


  • We thank the Natural Sciences and Engineering Research Council of Canada and DiaminoPharm Inc. for funding of the research.

Abstract

The highly stereoselective supramolecular self-assembly of α-amino acids with a chiral aldehyde derived from binol and a chiral guanidine derived from diphenylethylenediamine (dpen) to form the imino acid salt is reported. This system can be used to cleanly convert D-amino acids into L-amino acids or vice versa at ambient temperature. It can also be used to synthesize α-deuterated D- or L-amino acids. A crystal structure of the ternary complex together with DFT computation provided detailed insight into the origin of the stereoselective recognition of amino acids.

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