THE MATSUDA RESEARCH GROUP Department of Applied Chemistry
Tokyo University of Science

Hirotsugu Suzuki

Assistant Professor

Publication

• Rhodium-Catalysed Decarbonylative C(sp²)–H Alkylation of Indolines with Alkyl Carboxylic Acids and Carboxylic Anhydrides under Redox-Neutral Conditions
  Hirotsugu Suzuki, Yuya Kawai, Yosuke Takemura, and Takanori Matsuda
  Org. Biomol. Chem. 2022, 20, 2808–2812; DOI: 10.1039/D2OB00249C
  
  
• Rhodium-Catalyzed C(sp²)–H Alkoxycarbonylation/Acylation of Indolines with Anhydrides as a Carbonyl Source
  Hirotsugu Suzuki, Fumito Sasamori, and Takanori Matsuda
  Org. Lett. 2022, 24, 1141–1145; DOI: 10.1021/acs.orglett.1c04195
  
  
• Copper-Catalyzed Enantioselective Reductive Aldol Reaction of α,β-Unsaturated Carboxylic Acids to Ketones: Silanes as Activator and Transient Protecting Group
  Hirotsugu Suzuki, Kenji Yoneoka, Sora Kondo, and Takanori Matsuda
  Chem. Eur. J. 2022, 28, e202104273; DOI: 10.1002/chem.202104273
  
  

• Rhodium-Catalyzed Additive-Free C–H Ethoxycarbonylation of (Hetero)Arenes with Diethyl Dicarbonate as a CO Surrogate
  Hirotsugu Suzuki, Yumeng Liao, Yuya Kawai, and Takanori Matsuda
  Eur. J. Org. Chem. 2021, 4938–4942; DOI: 10.1002/ejoc.202100956
  
  

• Dealkoxylation of N-Alkoxyamides without an External Reductant Driven by Pd/Al Cooperative Catalysis
  Hirotsugu Suzuki, Takahiro Shiomi, Kenji Yoneoka, and Takanori Matsuda
  Org. Biomol. Chem. 2020, 18, 7545–7548; DOI: 10.1039/D0OB01815E
  
  

• Silver-catalyzed ring-opening [3+2] annulation of cyclopropenones with amides
  Takanori Matsuda, Yuki Tabata, and Hirotsugu Suzuki
  New J. Chem. 2018, 42, 19178–19182; DOI: 10.1039/c8nj04579h
  
  
• Catalytic alkylation reactions of weakly acidic carbonyl and related compounds using alkenes as electrophiles
  Yasuhiro Yamashita, Ryo Igarashi, Hirotsugu Suzuki, and Shū Kobayashi
  Org. Biomol. Chem. 2018, 16, 5969–5972; DOI: 10.1039/C8OB00941D
  
  
• Catalytic Direct-Type Addition Reactions of Alkylarenes with Imines and Alkenes
  Yasuhiro Yamashita, Hirotsugu Suzuki, Io Sato, Tsubasa Hirata, and Shū Kobayashi
  Angew. Chem., Int. Ed. 2018, 57, 6896–6900; DOI: 10.1002/anie.201711291
  
  

• Catalytic Direct-type 1,4-Addition Reactions of Alkylazaarenes
  Hirotsugu Suzuki, Ryo Igarashi, Yasuhiro Yamashita, and Shū Kobayashi
  Angew. Chem., Int. Ed. 2017, 56, 4520–4524; DOI: 10.1002/anie.201611374
  
  
• Catalytic Asymmetric Direct-Type 1,4-Addition Reactions of Alkanesulfonamides
  Yasuhiro Yamashita, Ryo Igarashi, Hirotsugu Suzuki, Shū Kobayashi
  Synlett 2017, 28, 1287–1290; DOI: 10.1055/s-0036-1588737
  
  

• Catalytic asymmetric direct-type 1,4-addition reactions of simple esters
  Io Sato, Hirotsugu Suzuki, Yasuhiro Yamashita, and Shū Kobayashi
  Org. Chem. Front. 2016, 3, 1241–1245; DOI: 10.1039/C6QO00242K
  
  

• Hafnium Trifluoromethanesulfonate [Hf(OTf)₄] as a Unique Lewis Acid in Organic Synthesis
  Haruro Ishitani, Hirotsugu Suzuki, Yuki Saito, Yasuhiro Yamashita, and Shū Kobayashi
  Eur. J. Org. Chem. 2015, 5485–5499; DOI: 10.1002/ejoc.201500423
  
  
• Catalytic Asymmetric 1,4-Addition Reactions of Simple Alkylnitriles
  Yasuhiro Yamashita, Io Sato, Hirotsugu Suzuki, and Shū Kobayashi
  Chem. Asian J. 2015, 10, 2143–2146; DOI: 10.1002/asia.201500405
  
  
• Catalytic Asymmetric Direct-Type 1,4-Addition Reactions of Simple Amides
  Hirotsugu Suzuki, Io Sato, Yasuhiro Yamashita, and Shū Kobayashi
  J. Am. Chem. Soc. 2015, 137, 4336–4339; DOI: 10.1021/jacs.5b01943
  
  

• Development of strong Brønsted base catalysis: catalytic direct-type Mannich reactions of non-activated esters via a product-base mechanism
  Yasuhiro Yamashita, Hirotsugu Suzuki, and Shū Kobayashi
  Org. Biomol. Chem. 2012, 10, 5750–5752; DOI: 10.1039/C2OB25522G