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Title: Three-step synthesis of cyclopropyl peptidomimetics. Author: Dunlap N, Lankford KR, Pathiranage AL, Taylor J, Reddy N, Gouger D, Singer P, Griffin K, Reibenspies J. Journal: Org Lett; 2011 Sep 16; 13(18):4879-81. PubMed ID: 21863816. Abstract: An efficient approach to novel cyclopropyl peptidomimetics has been developed. The synthetic route involves a cyclopropanation using ethyl (dimethylsulfuranylidene)acetate (EDSA) as the key step and affords a cyclopropyl peptidomimetic core in three steps from protected amino acid Weinreb amides.[Abstract] [Full Text] [Related] [New Search]