Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5224260 | Tetrahedron | 2009 | 6 Pages |
Abstract
Optically active α-amino 4H-[1,2,4]oxadiazol-5-ones (oxadiazolones) were prepared from optically active α-amino acids in five synthetic steps. The oxadiazolone moiety serves as a bioisosteric replacement for the carboxylic acid. Incorporation of an α-amino oxadiazolone into a representative dipeptide mimic is described.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
John E. Mangette, Matthew R. Johnson, Van-Duc Le, Rajesh A. Shenoy, Howard Roark, Michael Stier, Thomas Belliotti, Thomas Capiris, Peter R. Guzzo,