Enantioselective synthesis of novel, highly conformationally constrained peptide surrogates

DOI: 10.1016/S0957-4166(97)00265-6

Source and publish data:

Tetrahedron Asymmetry p. 2465 - 2471 (1997)

Update date:2022-09-26

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Authors:

Diaz, Miguel

Jimenez, Jose M.

Ortuno, Rosa M.

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Article abstract of DOI:10.1016/S0957-4166(97)00265-6

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,

Full text of DOI:10.1016/S0957-4166(97)00265-6

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