TY - JOUR
T1 - Enantioselective synthesis of novel, highly conformationally constrained peptide surrogates
AU - Díaz, Miguel
AU - Jiménez, José M.
AU - Ortuño, Rosa M.
PY - 1997/7/24
Y1 - 1997/7/24
N2 - 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.
AB - 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.
U2 - 10.1016/S0957-4166(97)00265-6
DO - 10.1016/S0957-4166(97)00265-6
M3 - Article
SN - 0957-4166
VL - 8
SP - 2465
EP - 2471
JO - Tetrahedron Asymmetry
JF - Tetrahedron Asymmetry
IS - 14
ER -