Takeshi Nanjo

发表

Synthesis of 3-acyl-2-arylindole via palladium-catalyzed isocyanide insertion and oxypalladation of alkyne.

C. Tsukano, Y. Takemoto, Takeshi Nanjo, 2013, Organic letters.

A Pyridine-Based Donor–Acceptor Molecule: A Highly Reactive Organophotocatalyst That Enables the Reductive Cleavage of C–Br Bonds through Halogen Bonding

Y. Takemoto, Takeshi Nanjo, N. Kato, 2022, ACS Catalysis.

Boronic Acid‐Mediated Photocatalysis Enables the Intramolecular Hydroacylation of Olefins Using Carboxylic Acids

Y. Takemoto, Takeshi Nanjo, Taichi Yumura, 2022, European Journal of Organic Chemistry.

Remote, Late-Stage Oxidation of Aliphatic C-H Bonds in Amide-Containing Molecules.

M. White, Takeshi Nanjo, E. C. de Lucca, 2017, Journal of the American Chemical Society.

Domino Pd-catalyzed Heck cyclization and bismuth-catalyzed hydroamination: formal synthesis of elacomine and isoelacomine.

C. Tsukano, Y. Takemoto, Takeshi Nanjo, 2011, Chemistry.

Photocatalytic Activation of Elemental Sulfur Enables a Chemoselective Three-Component Thioesterification.

Y. Takemoto, Takeshi Nanjo, S. Murakami, 2021, Organic letters.

Chemoselective methylene oxidation in aromatic molecules

Jinpeng Zhao, M. White, Takeshi Nanjo, 2018, Nature Chemistry.

Total Synthesis of Lyconesidine B, a Lycopodium Alkaloid with an Oxygenated, Amine-Type Fawcettimine Core.

Tomohiro Kurose, C. Tsukano, Y. Takemoto, 2020, Organic letters.

Palladium-catalyzed cascade process consisting of isocyanide insertion and benzylic C(sp3)-H activation: concise synthesis of indole derivatives.

C. Tsukano, Y. Takemoto, Takeshi Nanjo, 2012, Organic letters.

Divergent and Scalable Synthesis of α-Hydroxy/Keto-β-amino Acid Analogues by the Catalytic Enantioselective Addition of Glyoxylate Cyanohydrin to Imines

Xuan Zhang, Y. Takemoto, Takeshi Nanjo, 2019, ACS Catalysis.

A Hydroperoxide-Mediated Decarboxylation of α-Ketoacids Enables the Chemoselective Acylation of Amines.

Xuan Zhang, Y. Takemoto, Takeshi Nanjo, 2019, Chemistry.

Highly Stereoselective, Organocatalytic Mannich-type Addition of Glyoxylate Cyanohydrin: A Versatile Building Block for the Asymmetric Synthesis of β-Amino-α-ketoacids

Y. Takemoto, Takeshi Nanjo, Y. Tokuhiro, 2022, ACS Catalysis.

Photocatalytic C-O Bond Cleavage of Alcohols Using Xanthate Salts.

Y. Takemoto, Takeshi Nanjo, Tatsuki Matsugasako, 2021, Organic letters.

Mild and Chemoselective Thioacylation of Amines Enabled by the Nucleophilic Activation of Elemental Sulfur.

M. Saito, Yusuke Kobayashi, Y. Takemoto, 2020, Journal of the American Chemical Society.

Oxidative Decarboxylation Enables Chemoselective, Racemization-Free Esterification: Coupling of α-Ketoacids and Alcohols Mediated by Hypervalent Iodine(III).

Y. Takemoto, Takeshi Nanjo, N. Kato, 2018, Organic letters.

Palladium-Catalyzed Double C-H Functionalization of Arenes at the Positions ortho and meta to Their Directing Group: Concise Synthesis of Benzocyclobutenes.

C. Tsukano, Y. Takemoto, Takeshi Nanjo, 2016, Chemical & pharmaceutical bulletin.

Synthesis of 3,3-Disubstituted 2-Aminoindolenines by Palladium-Catalyzed Allylic Amidination with Isocyanide

C. Tsukano, Y. Takemoto, Takeshi Nanjo, 2014, Synlett.

Remote, Late-Stage Oxidation of Aliphatic C-H Bonds in Amide-Containing Molecules.

M. White, Takeshi Nanjo, E. C. de Lucca, 2017, Journal of the American Chemical Society.

Bulky Alkyl Substituents Enhance the Photocatalytic Activity of Pyridine-Based Donor-Acceptor Molecules in the Direct Reductive Cleavage of the C-Br Bond of Aliphatic Bromides.

Y. Takemoto, Takeshi Nanjo, Natsuki Kato, 2024, Organic letters.

A Benzophenothiazine/Boronic Acid Hybrid Photocatalyst Enables the Single Electron Transfer (SET) to Carboxy Groups: SET-Initiated Cyclization of α,β-Unsaturated Carboxylic Acids

Y. Takemoto, Takeshi Nanjo, Taichi Yumura, 2023, ACS Catalysis.

Synthesis of Chlorinated Oligopeptides via γ- and δ-Selective Hydrogen Atom Transfer Enabled by the N-Chloropeptide Strategy.

Y. Takemoto, Takeshi Nanjo, Ayaka Matsumoto, 2023, Journal of the American Chemical Society.