Hirotsugu Suzuki

Assistant Professor

University of Fukui

Japan

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Hirotsugu Suzuki is an Assistant Professor at the University of Fukui in Japan. His research focuses on organic synthesis methods, particularly in the development of innovative strategies involving radical reactions and functionalization of (hetero)arenes. Recent articles highlight his work on photoinduced decarboxylation and mechanistic studies in photoredox systems that enhance synthetic capabilities. His contributions significantly advance the field of synthetic organic chemistry.

Hirotsugu Suzuki

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Articles (27)

Mechanistic Insight into the Photoinduced Decarboxylative Radical Addition of Carboxylic Acid to Alkenes in a Two-Molecule Photoredox System

Strategy for the Synthesis of Phenylalanine Derivatives through the Addition of Aryl Radicals to Dehydroamino Acid via Photoinduced Decarboxylation or Deboronation

Reverse Regioselective Dicarbofunctionalization via <i>Anti</i>‐Michael‐Type Addition

C(sp2)-H Functionalization of (Hetero)arenes with Carboxylic Acid Anhydrides

Regio‐ and Enantioconvergent Hydroallylation of Acrylates Enabled by γ‐Silyl‐Substituted Allyl Acetates

Visible Light–Induced Decarboxylative Radical Addition of Heteroaromatic Carboxylic Acids to Alkenes at Room Temperature in Two‐Molecule Photoredox System

Ring Expansion from 16‐Membered Macrocyclic Lactones Using Yamaguchi and Photoinduced Decarboxylative Radical Macrolactonization

Palladium-Catalyzed anti-Michael-Type Hydroamination of N-(Quinolin-8-yl)acrylamide with 2-Pyridones

Double difunctionalization of vinyl ether tethered nucleophile with electron-deficient alkene in two-molecule photoredox system

Palladium-Catalyzed anti-Michael-Type (Hetero)arylation of Acrylamides

Amide-Directed Rhodium-Catalyzed Chain-Walking Hydrothiolation of Internal Alkenes

Rhodium-Catalyzed Decarbonylative Intramolecular Arylation of 2-(1H-Indole-1-carbonyl)benzoic Acids

Modular synthesis of 3,3-disubstituted oxindoles from nitrones and acrylic acids

Rhodium-catalysed additive-free alkoxycarbonylation of indoles: 2,4,6-trimethylbenzoic acid-based carbonate anhydrides as a versatile alkoxycarboxyl source

Rhodium-catalysed additive-free carbonylation of benzamides with diethyl dicarbonate as a carbonyl source

Benzoic Acid Serves as Precursor of Catalytic HAT Reagent in a Two-Molecule Photoredox System

Rhodium-Catalyzed Intramolecular Acylation of 2-(Indol-1-yl)-benzoic Acids under Redox-Neutral Conditions

Effects of Electron-Donor and Counter-Cation in Photoinduced Deboronative and Decarboxylative Aryl Radical Generation Using Two-Molecule Photoredox Catalysts

Diastereo‐ and Enantioselective Reductive Mannich‐type Reaction of α,β‐Unsaturated Carboxylic Acids to Ketimines: A Direct Entry to Unprotected β2,3,3‐Amino Acids

Photoinduced radical generation and trapping by acrylonitrile of N-Boc secondary amine and N-Boc N-methyl α-amino acid ester at α-position using two-molecule photoredox catalysts

Rhodium-catalyzed C6-Selective Alkoxycarbonylation of Pyridones

Copper‐Catalyzed Enantioselective Reductive Aldol Reaction of α,β‐Unsaturated Carboxylic Acids to Alkyl Aryl Ketones: Silanes as Activator and Transient Protecting Group

Rhodium-Catalyzed C(sp2)–H Alkoxycarbonylation/Acylation of Indolines with Anhydrides as a Carbonyl Source

Rhodium-catalysed decarbonylative C(sp2)–H alkylation of indolines with alkyl carboxylic acids and carboxylic anhydrides under redox-neutral conditions

Rhodium-Catalyzed Additive-Free C−H Ethoxycarbonylation of (Hetero)Arenes with Diethyl Dicarbonate as a CO Surrogate

Dealkoxylation ofN-alkoxyamides without an external reductant driven by Pd/Al cooperative catalysis

Dealkoxylation of N-alkoxyamides without an external reductant driven by Pd/Al cooperative catalysis

Collaborators (3)

Takanori Matsuda

Yasuharu Yoshimi

Yasunori Matsui

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