Takumi Abe

Lecturer

Okayama University

Japan

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Takumi Abe is a Lecturer at Okayama University in Japan. His research interests encompass synthetic organic chemistry, particularly focusing on indolines and their derivatives, as well as the pharmaceutical applications of traditional herbal medicines. His recent publications explore innovative synthesis methods including the production of deaminokynurenines and the development of azidoindoles.

Takumi Abe

Research Interests

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Articles (28)

2‐Hydroxy‐3‐(Pyrrolidin‐1‐yl)‐Indolines: A Platform for Accessing Decorated Deaminokynurenines Enabled by a Double Tautomeric Control

Molecular Iodine-Catalyzed Synthesis of 3,3-Disubstituted Isatins: Total Synthesis of Indole Alkaloid, 3,3-Dimethoxy-2-oxindole

Potassium tert‐Butoxide‐Mediated Ring‐Opening of Indolines: Concise Synthesis of 2‐Vinylanilines

One-pot synthesis of trans-2,3-diaminoindolines through 2,3-diamination of electrophilic indolines

One-pot Synthesis of trans-2,3-Diaminoindolines through 2,3-Diamination of Electrophilic Indolines

Revisiting 3-azidoindoles: overcoming the trade-off challenges between stability and reactivity of in situ-generated azidoindoles

Formal One Carbon Deletion of Indoline Hemiaminals under Tautomeric Control to Access 2-Aminobenzyl Compounds

Azidoindolines—From Synthesis to Application: A Review

Switchable Synthesis of 3-Aminoindolines and 2’-Aminoarylacetic Acids Using Grignard Reagents and 3-Azido-2-hydroxyindolines

Switchable synthesis of 3-aminoindolines and 2′-aminoarylacetic acids using Grignard reagents and 3-azido-2-hydroxyindolines

Concise Synthesis of Thiazolo[4,5‐b]indoles via Ring Switch/Cyclization Sequences

Indoline hemiaminals: a platform for accessing anthranilic acid derivatives through oxidative deformylation

On Demand Synthesis of C3-N1' Bisindoles by a Formal Umpolung Strategy: First Total Synthesis of (±)-Rivularin A

On Demand Synthesis of C3−N1’ Bisindoles by a Formal Umpolung Strategy: First Total Synthesis of (±)‐Rivularin A

Synthetic strategies for the construction of C3–N1′ bisindoles

Perspectives of traditional herbal medicines in treating retinitis pigmentosa

Indoline hemiaminals: a platform for accessing anthranilic acid derivatives through oxidative deformylation

Oxytrofalcatin Puzzle: Total Synthesis and Structural Revision of Oxytrofalcatins B and C

One-Pot Synthesis of Core Structure of Shewanelline C Using an Azidoindoline

Aluminum-Catalyzed Cross Selective C3–N1′ Coupling Reactions of N-Methoxyindoles with Indoles

Synthesis of Spiro[indole-3,3′-pyrrolidine]-2′-(thi)ones

Revisiting Cryptocyanine Dye, NK-4, as an Old and New Drug: Review and Future Perspectives

Total Synthesis of the Proposed Structure of Indolyl 1,2-Propanediol Alkaloid, 1-(1H-Indol-3-yloxy)propan-2-ol

First Total Synthesis of Reassigned Echinosulfonic Acid D

Indole Editing Enabled by HFIP‐Mediated Ring‐Switch Reactions of 3‐Amino‐2‐Hydroxyindolines

Traditional Chinese Medicines and Prescriptions Brought from China to Japan by a Monk (Jianzhen, Japanese: Ganjin): A Historical Review

Indole Editing Enabled by HFIP-Mediated Ring-Switch Reactions of 3-Amino-2-Hydroxyindolines

Chemo- and Site-Selective Replacement of N-Terminal Carbamates in Peptides

Collaborators (6)

Masafumi Ueda

Toshihiko Matsuo

Shihui Liu

Toshiki Yamashiro

Motohiro Yasui

Daisuke Sawada

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