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Precision Chemistry|August 29, 2025
An Unusual Acceleration of Amination Reactivity by the Proximal Ester Groups in Catechol Diesters: An Efficient Way for Peptide SynthesisAn Wu, Hirotaka Ikeda, Hisashi YamamotoOrganic Letters|July 17, 2004
Tin(IV) chloride-chiral pyrogallol derivatives as new Lewis acid-assisted chiral Brønsted acids for enantioselective polyene cyclizationKeiko Kumazawa, Kazuaki Ishihara, Hisashi YamamotoJournal of the American Chemical Society|July 17, 2019
Substrate-Directed Lewis-Acid Catalysis for Peptide SynthesisWataru Muramatsu, Tomohiro Hattori, Hisashi YamamotoJournal of the American Chemical Society|May 13, 2004
Enantioselective tandem O-nitroso Aldol/Michael reactionYuhei Yamamoto, Norie Momiyama, Hisashi YamamotoEuropean Journal of Organic Chemistry|December 17, 2009
Enantioselective Ag-Catalyzed Allylation of AldiminesMarina Naodovic, Manabu Wadamoto, Hisashi YamamotoOrganic Letters|October 21, 2005
N-alkyl-4-boronopyridinium halides versus boric acid as catalysts for the esterification of alpha-hydroxycarboxylic acidsToshikatsu Maki, Kazuaki Ishihara, Hisashi YamamotoChemical Communications (Cambridge, England)|June 14, 2021
Amide bond formation: beyond the dilemma between activation and racemisationWataru Muramatsu, Tomohiro Hattori, Hisashi YamamotoChemistry, an Asian Journal|June 21, 2008
Lewis acid catalyzed benzylic brominationKazutaka Shibatomi, Yanhua Zhang, Hisashi YamamotoThe Journal of Organic Chemistry|December 10, 2025
Peptide Bond Formation through Fragment Condensation with Silylating ReagentsKotaro Ishihara, Tomohiro Hattori, Hisashi YamamotoOrganic Letters|March 31, 2025
Triphenyl Phosphite-Mediated One-Pot Peptide-Bond Formation under Neutral Reaction ConditionsTomohiro Hattori, Tomomi Ishiguro, Hisashi YamamotoPageof 29