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Critical chain length for the formation of α- and β-polypeptide conformations in the solid state. Syntheses and conformations of oligopeptides with alternate L-alanyl and L-leucyl residues. Ryoichi Katakai , J. Chem. Soc., Perkin Trans. 1 , 1979 , 905

Chain ends as supports for α-helical structures in oligopeptides. Ryoichi Katakai , J. Chem. Soc., Chem. Commun. , 1978 , 692

Use of the dehydrophos biosynthetic enzymes to prepare antimicrobial analogs of alaphosphin. Despina J. Bougioukou, Chi P. Ting, Spencer C. Peck, Subha Mukherjee, Wilfred A. van der Donk , Org. Biomol. Chem. , 2019 , 17 , 822

Critical chain length for the formation of the α-helix in the solid state. Synthesis and conformation of sequential oligopeptides and a polypeptide containing the sequence L-leucyl-L-alanyl-L-leucylglycine. Ryoichi Katakai , J. Chem. Soc., Perkin Trans. 1 , 1977 , 1193

Deprotection/reprotection of the amino group in α-amino acids and peptides. A one-pot procedure in [Bmim][BF4] ionic liquid. M. L. Di Gioia, A. Barattucci, P. Bonaccorsi, A. Leggio, L. Minuti, E. Romio, A. Temperini, C. Siciliano , RSC Adv. , 2014 , 4 , 2678

Kinetic enantioselectivity of a protonated bis(diamido)-bridged basket resorcin[4]arene towards alanine peptides. C. Fraschetti, M. Montagna, M. E. Crestoni, A. Calcaterra, F. Aiello, L. Santi, A. Filippi , Org. Biomol. Chem. , 2017 , 15 , 1183

Assignment of the far-infrared band characteristic of L-methionine with α-helical conformation. Ryoichi Katakai, Yasuko Lizuka , J. Chem. Soc., Chem. Commun. , 1982 , 1027

Protected decapeptide ortho-nitrophenylsulphenyl–(L-leucyl–L-alanyl)5–ethyl ester [nps–(L-leu–L-ala)5–OEt]. Shortest critical peptide size for development of the α-helix in the solid state. Ryoichi Katakai, Yohko Nakayama , J. Chem. Soc., Chem. Commun. , 1977 , 805

An update on new methods to synthesize cyclotetrapeptides. Luis M. De Leon Rodriguez, Andreas J. Weidkamp, Margaret A. Brimble , Org. Biomol. Chem. , 2015 , 13 , 6906

Synthesis of terminal N-thiobenzoyl peptides by use of 4-substituted 2-phenylthiazol-5(4H)-ones as acylating agents for amino-acids and peptides. Optically-active 4-substituted 2-phenylthiazol-5(4H)-ones. G. C. Barrett , J. Chem. Soc. C , 1971 , 1380