Takanori Matsuda

Professor

University of Tokyo

Japan

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Professor Takanori Matsuda is a faculty member at Tokyo University of Science, Japan. His research interests focus on organic chemistry, particularly in catalytic reactions involving palladium and rhodium, as evidenced by his recent publications on decarbonylation, hydroamination, and the synthesis of oxindoles. His work also explores innovative methods in enantioselective synthesis, contributing significantly to advancements in the field.

Takanori Matsuda

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Articles (18)

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

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

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

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

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

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

Diastereo- and Enantioselective Reductive Mannich-type Reaction of <i>α</i>,<i>β</i>-Unsaturated Carboxylic Acids to Ketimines: A Direct Entry to Unprotected <i>β</i><SUP>2,3,3</SUP>-Amino Acids

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

Rhodium(I)‐Catalyzed Arylative Annulation of β‐Alkynyl Ketones for Preparation of Fused Aromatics

Ruthenium-catalysed cyclisation reactions of 1,11-dien-6-ynes leading to biindenes

Synthesis of unsymmetrical benzils via palladium-catalysed α-arylation–oxidation of 2-hydroxyacetophenones with aryl bromides

Collaborators (1)

Hirotsugu Suzuki

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