Naohiko Yoshikai

Professor

Tohoku University

Japan

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About

Naohiko Yoshikai is a Professor at Tohoku University in Japan. His research focuses on organic synthesis, specifically in the areas of cyclopropylation, atropisomerism, and the development of new methodologies for the synthesis of complex organic molecules. Recent publications include work on stereocontrolled access to amino alcohols and regioselective methodologies for polycyclic aromatics.

Articles (24)

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2025

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2022

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2022

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2022

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2021

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2021

Collaborators (4)

Shingo Ito

Assistant Professor

Nanyang Technological University (NTU)

SINGAPORE

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Kazuya Kanemoto

JAPAN

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Eunsang Kwon

Associate Professor

Tohoku University

JAPAN

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Jun Kikuchi

Assistant Professor

Tohoku University

JAPAN

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Naohiko Yoshikai

Research Interests

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About

Articles (24)

Iodine(III)-Mediated Cyclization Cascade of Diynes to Benzofulvene Derivatives

Stable and responsive atropisomerism around a carbon–iodine bond

Formal Cyclopropylation of Imines with Cyclopropanols: Stereocontrolled Access to Conformationally Constrained γ‐Amino Alcohols

Formal Cyclopropylation of Imines with Cyclopropanols: Stereocontrolled Access to Conformationally Constrained γ‐Amino Alcohols

Hexadehydro Diels–Alder/Alkynyliodanation Cascade: A Highly Regioselective Entry to Polycyclic Aromatics

A versatile entry to unnatural, disulfide-linked amino acids and peptides through the disulfuration of azlactones

Diazomethyl-λ3-iodane meets aryne: dipolar cycloaddition and C-to-N iodane shift leading to indazolyl-λ3-iodanes

Amino‐ and Alkoxybenziodoxoles: Facile Preparation and Use as Arynophiles

Three-component N-alkenylation of azoles with alkynes and iodine(III) electrophile: synthesis of multisubstituted N-vinylazoles

Carboiodanation of Arynes: Organoiodine(III) Compounds as Nucleophilic Organometalloids

Three-component Friedel–Crafts-type difunctionalization of ynamides with (hetero)arenes and iodine(iii) electrophile

Stereoselective Hydroxyallylation of Cyclopropenes with Cyclopropanols via NHC Catalysis of Transient Organozinc Species

Stereoselective Hydroxyallylation of Cyclopropenes with Cyclopropanols via NHC Catalysis of Transient Organozinc Species

Site‐Selective C−H Alkenylation of N‐Heteroarenes by Ligand‐Directed Co/Al and Co/Mg Cooperative Catalysis**

Site‐Selective C–H Alkenylation of N‐Heteroarenes by Ligand‐Directed Co/Al and Co/Mg Cooperative Catalysis

Zinc‐Mediated Diastereoselective Annulation of Cyclopropanols with Alkylidenemalononitriles via Enolized Homoenolate

Stereoselective Approach to Multisubstituted Enolates from Unactivated Alkynes: Oxyalkylidenation of Alkynyl Ketone Enolates with Aldehydes

Stereoselective Synthesis of β-Alkoxy-β-amido Vinylbenziodoxoles via Iodo(III)etherification of Ynamides

Cobalt selectively annulates

Cobalt-Catalyzed Carbo- and Hydrocyanation of Alkynes via C–CN Bond Activation

Zinc-Mediated Hydroxyallylation of Aldehydes with Cyclopropanols: Direct Access to Vicinal anti-sec,tert-Diols via Enolized Homoenolates

Regio- and Stereoselective Synthesis of Enol Carboxylate, Phosphate, and Sulfonate Esters via Iodo(III)functionalization of Alkynes

Zinc-Catalyzed β-Functionalization of Cyclopropanols via Enolized Homoenolate

Iron-Catalyzed Remote C–H Alkylation of 8-Amidoquinolines with Cycloalkanes

Collaborators (4)

Shingo Ito

Kazuya Kanemoto

Eunsang Kwon

Jun Kikuchi

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