Enantioselective synthesis of novel, highly conformationally constrained peptide surrogates

Miguel Díaz, José M. Jiménez, Rosa M. Ortuño

Research output: Contribution to journalArticleResearchpeer-review

24 Citations (Scopus)

Abstract

Two new enantiomeric peptide surrogates as well as a tripeptide, all of them having highly conformationally constrained structures, have been synthesized. (Z)-cyclo-Aspartic acid and convenient α-substituted isoserine derivatives, in both antipodal forms, as well as methyl (R)-2-phenylglycinate, have been used as the monomeric units.
Original languageEnglish
Pages (from-to)2465-2471
JournalTetrahedron Asymmetry
Volume8
Issue number14
DOIs
Publication statusPublished - 24 Jul 1997

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