Hisashi Yamamoto

Research interests

Publications

• A Brønsted Acid Catalyst for the Enantioselective Protonation Reaction

  Journal of the American Chemical Society · 2008 · 10.1021/ja8041542

• Catalytic Enantioselective Pudovik Reaction of Aldehydes and Aldimines with Tethered Bis(8-quinolinato) (TBOx) Aluminum Complex

  Journal of the American Chemical Society · 2008 · 10.1021/ja803859p

• Design of Chiral N-Triflyl Phosphoramide as a Strong Chiral Brønsted Acid and Its Application to Asymmetric Diels−Alder Reaction

  Journal of the American Chemical Society · 2006 · https://doi.org/10.1021/ja062508t

• Silver-Catalyzed Asymmetric Sakurai−Hosomi Allylation of Ketones

  Journal of the American Chemical Society · 2005 · 10.1021/ja0553351

• Brønsted Acid Catalysis of Achiral Enamine for Regio- and Enantioselective Nitroso Aldol Synthesis

  Journal of the American Chemical Society · 2005 · 10.1021/ja0444637

• Cyanuric Chloride as a Mild and Active Beckmann Rearrangement Catalyst

  Journal of the American Chemical Society · 2005 · 10.1021/ja053441x

• Kombinierte Säurekatalyse in der asymmetrischen Synthese durch “Designer‐Säuren”

  Angewandte Chemie · 2005 · 10.1002/ange.200460394

• Enantioselective Epoxidation of Allylic Alcohols by a Chiral Complex of Vanadium: An Effective Controller System and a Rational Mechanistic Model

  Angewandte Chemie International Edition · 2005 · 10.1002/anie.200500938

• Rich chemistry of nitroso compounds

  Chemical Communications · 2005 · 10.1039/b503212c

• “Designer Acids”: Combined Acid Catalysis for Asymmetric Synthesis

  Angewandte Chemie International Edition · 2005 · https://doi.org/10.1002/anie.200460394

• Axially Chiral Biaryl Diols Catalyze Highly Enantioselective Hetero-Diels−Alder Reactions through Hydrogen Bonding

  Journal of the American Chemical Society · 2005 · 10.1021/ja044076x

• Asymmetric Direct Aldol Reaction Assisted by Water and a Proline‐Derived Tetrazole Catalyst

  Angewandte Chemie International Edition · 2004 · https://doi.org/10.1002/anie.200352724

• Enantioselective Tandem O-Nitroso Aldol/Michael Reaction

  Journal of the American Chemical Society · 2004 · 10.1021/ja049741g

• Enantioselective O - and N -Nitroso Aldol Synthesis of Tin Enolates. Isolation of Three BINAP−Silver Complexes and Their Role in Regio- and Enantioselectivity

  Journal of the American Chemical Society · 2004 · 10.1021/ja039103i

• Catalytic Enantioselective Synthesis of α-Aminooxy and α-Hydroxy Ketone Using Nitrosobenzene

  Journal of the American Chemical Society · 2003 · 10.1021/ja0298702

• Rhenium(VII) Oxo Complexes as Extremely Active Catalysts in the Dehydration of Primary Amides and Aldoximes to Nitriles

  Angewandte Chemie International Edition · 2002 · 10.1002/1521-3773(20020816)41:16<2983::aid-anie2983>3.0.co;2-x

• Direct Condensation of Carboxylic Acids with Alcohols Catalyzed by Hafnium(IV) Salts

  Science · 2000 · 10.1126/science.290.5494.1140

• Arylboron Compounds as Acid Catalysts in Organic Synthetic Transformations

  European Journal of Organic Chemistry · 1999 · 10.1002/(sici)1099-0690(199903)1999:3<527::aid-ejoc527>3.0.co;2-r

• 3,4,5-Trifluorobenzeneboronic Acid as an Extremely Active Amidation Catalyst

  The Journal of Organic Chemistry · 1996 · https://doi.org/10.1021/jo9606564

• Scandium Trifluoromethanesulfonate as an Extremely Active Lewis Acid Catalyst in Acylation of Alcohols with Acid Anhydrides and Mixed Anhydrides

  The Journal of Organic Chemistry · 1996 · https://doi.org/10.1021/jo952237x

• Catalytic Asymmetric Allylation of Aldehydes Using a Chiral Silver(I) Complex

  Journal of the American Chemical Society · 1996 · 10.1021/ja9603315

• Scandium Trifluoromethanesulfonate as an Extremely Active Acylation Catalyst

  Journal of the American Chemical Society · 1995 · 10.1021/ja00120a030

• Asymmetric hetero-Diels-Alder reaction catalyzed by a chiral organoaluminum reagent

  Journal of the American Chemical Society · 1988 · https://doi.org/10.1021/ja00209a061

• Amphiphilic reactions by means of exceptionally bulky organoaluminum reagents. Rational approach for obtaining unusual equatorial, anti-Cram, and 1,4 selectivity in carbonyl alkylation

  Journal of the American Chemical Society · 1988 · 10.1021/ja00219a038

• Organoaluminum-promoted Beckmann rearrangement of oxime sulfonates

  Journal of the American Chemical Society · 1983 · https://doi.org/10.1021/ja00347a052

Current projects

No projects listed.