Peptides from chiral Calpha,alpha-disubstituted glycines : crystallographic characterization of conformation of Calpha-methyl, Calpha-isopropylglycine [(alphaMe)Val] in simple derivatives and model peptides
The mol. and crystal structures of R-L-(aMe)Val-R1 [R = ClCH2CO, R1 = OH; R = Z, R1 = Ala-Ala-OMe (I); R = Ac-Aib-Aib, Z-Aib, R1 = Aib-Aib-OCMe3; (aMe)Val = NHCMe(CHMe2)CO; Z = PhCH2O2C; Aib = NHCMe2CO] were detd. by x-ray diffraction. Tripeptide I adopts a type-I b-turn conformation stabilized by a
