E. Mossel

Cα-Methyl phenylglycine-based semi-synthetic ampicillin and cephalexin analogues

C. Toniolo, F. Formaggio, M. Crisma, 2004, Letters in Peptide Science.

(alphaMe)Aun: a highly lipophilic, chiral, Calpha-tetrasubstituted alpha-amino acid. Incorporation into model peptides and preferred conformation.

C. Toniolo, F. Formaggio, M. Crisma, 2000, The journal of peptide research : official journal of the American Peptide Society.

Mag: a Cα-Methylated, Side-chain Unsaturated α-Amino Acid. Introduction into Model Peptides and Conformational Preference

C. Toniolo, F. Formaggio, M. Crisma, 2000 .

Comparative conformational analysis of peptides based on the two Cα-tetrasubstituted, Cβ-branched, chiral α-amino acids (αMe)Dip and (αMe)Val

C. Toniolo, F. Formaggio, M. Crisma, 2000 .

Aspartame dipeptide analogues: effect of number of side-chain methylene group spacers and Cα-methylation in the second position

C. Toniolo, F. Formaggio, M. Crisma, 1997 .

Cα-Methyl, Cα-phenylglycine peptides: A structural study

C. Toniolo, F. Formaggio, M. Crisma, 1998, Letters in Peptide Science.

Effect of phenyl ring position in the Cα‐methylated α‐amino acid side chain on peptide preferred conformation

C. Toniolo, F. Formaggio, M. Crisma, 1996 .

Mag: A Cα-Methylated, Side-Chain Unsaturated α-Amino Acid. Introduction into Model Peptides and Conformational Preference.

C. Toniolo, F. Formaggio, M. Crisma, 2000 .