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- W2077809230 abstract "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." @default.
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- W2077809230 date "1997-07-01" @default.
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- W2077809230 title "Enantioselective synthesis of novel, highly conformationally constrained peptide surrogates" @default.
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- W2077809230 doi "https://doi.org/10.1016/s0957-4166(97)00265-6" @default.
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