@article{oai:nagasaki-u.repo.nii.ac.jp:00002524,
 author = {Furukawa, Kaori and Oba, Makoto and Toyama, Kotomi and Opiyo, George Ouma and Demizu, Yosuke and Kurihara, Masaaki and Doi, Mitsunobu and Tanaka, Masakazu},
 issue = {30},
 journal = {Organic and Biomolecular Chemistry},
 month = {Aug},
 note = {We developed a novel methodology using cyclic α,α-disubstituted α-amino acids (dAAs) with an acetal-side chain to control peptide secondary structures. The introduction of cyclic dAAs into peptides contributed to the stabilization of peptide secondary structures as a helix, while an acidic treatment of peptides resulted in a marked conformational change., Organic and Biomolecular Chemistry, 15(30), pp.6302-6305; 2017},
 pages = {6302--6305},
 title = {Low pH-triggering changes in peptide secondary structures},
 volume = {15},
 year = {2017}
}