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The Journal of Organic Chemistry|December 4, 2019
One Step Synthesis of Fmoc-Aminoacyl-N-alkylcysteine via the Ugi Four-Component Condensation ReactionYuya Asahina, Hironobu HojoJournal of Peptide Science : an Official Publication of the European Peptide Society|September 30, 2011
Chemical synthesis of the S-linked glycopeptide, sublancinHidekazu Katayama, Yuya Asahina, Hironobu HojoChemical Communications (Cambridge, England)|January 31, 2017
One-pot native chemical ligation by combination of two orthogonal thioester precursorsYuya Asahina, Toru Kawakami, Hironobu HojoOrganic & Biomolecular Chemistry|February 2, 2024
The dipicolylamino group as an efficient leaving group for amide bond formation via hexafluoroisopropyl esterYasuhito Akai, Yuya Asahina, Hironobu HojoChemistry (Weinheim an Der Bergstrasse, Germany)|January 10, 2018
Sialyl Tn Unit with TFA-Labile Protection Realizes Efficient Synthesis of Sialyl GlycoproteinNaoki Takeda, Toshiki Takei, Yuya Asahina, et al.Organic Letters|May 18, 2026
Chemical Synthesis of Difucosylated Glycopeptide by the Combination of Substituted Benzyl and Levulinoyl Protecting GroupsYuya Asahina, Kenta Nagahama, Tomoya Shidawara, et al.Organic & Biomolecular Chemistry|September 24, 2013
Fast preparation of an N-acetylglucosaminylated peptide segment for the chemoenzymatic synthesis of a glycoproteinYuya Asahina, Mika Kanda, Akemi Suzuki, et al.The Journal of Physical Chemistry. B|December 21, 2013
Model study using designed selenopeptides on the importance of the catalytic triad for the antioxidative functions of glutathione peroxidaseToshiki Takei, Yoshiko Urabe, Yuya Asahina, et al.Organic & Biomolecular Chemistry|August 16, 2011
Efficient preparation of Fmoc-aminoacyl-N-ethylcysteine unit, a key device for the synthesis of peptide thioestersHironobu Hojo, Hajime Kobayashi, Risa Ubagai, et al.The FEBS Journal|October 25, 2022
Structural dynamics of the N-terminal SH2 domain of PI3K in its free and CD28-bound statesYuhi Hosoe, Yohei Miyanoiri, Suyong Re, et al.Pageof 2