Nozomi Saito

Meiji Pharmaceutical University

Japan

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Articles (9)

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

The first synthesis of N -(acyloxy)ynamides was realized through the coupling of N -(acyloxy)amides and hypervalent alkynyliodane under mild conditions.

Year:

2023

Year:

2023

Year:

2021

Collaborators (3)

kakeru matsukuma

Meiji Pharmaceutical University

JAPAN

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Masanori Tayu

Assistant professor

Meiji Pharmaceutical University

JAPAN

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Masahiro Noji

Associate Professor

Meiji Pharmaceutical University

JAPAN

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Nozomi Saito

Research Interests

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Articles (9)

Aminoalkylation of Alkenes for Modular Pyrrolidine Synthesis <i>via</i> Electron Donor–Acceptor Complexes Generated from Alkenes and Amine-Tethered <i>N</i>-Hydroxyphthalimide Esters

Catalytic Synthesis of Azepinoindoles from Ynamides Containing Indolyl Moieties <i>via</i> Ruthenium–Vinylidene Species

Switchable Four- and Five-Component Reactions with Perfect Regioselectivity Promoted by Photoredox/Sulfide Dual-Catalytic Quenching for Access to Diverse Complex Imides

A General Catalytic Sulfide‐based Electron Donor–Acceptor Complex Platform for Decarboxylative Transformations of N‐Hydroxyphthalimide Esters

Photoredox/Sulfide Dual Catalysis for Modular Synthesis of Multi‐substituted Furan Rings via Catalytic Indirect Reductive Quenching

Photoredox catalysis using methoxyarenes: mechanistic studies and synthetic applications

Synthesis of<i>N</i>-(acyloxy)-<i>N</i>-alkynylamides<i>via</i>generation of “C<sub>2</sub>” from hypervalent alkynyliodane and a weak base

A Photoredox/Sulfide Dual Catalysis System That Uses Sulfide Radical Cations to Promote Alkene Chlorotrifluoromethylation

A Catalytic Construction of Indoles via Formation of Ruthenium Vinylidene Species from N‐Arylynamides

Collaborators (3)

kakeru matsukuma

Masanori Tayu

Masahiro Noji

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Nozomi Saito

Research Interests

Explore related searches

Contact this professor

Articles (9)

Aminoalkylation of Alkenes for Modular Pyrrolidine Synthesis &lt;i&gt;via&lt;/i&gt; Electron Donor–Acceptor Complexes Generated from Alkenes and Amine-Tethered &lt;i&gt;N&lt;/i&gt;-Hydroxyphthalimide Esters

Catalytic Synthesis of Azepinoindoles from Ynamides Containing Indolyl Moieties &lt;i&gt;via&lt;/i&gt; Ruthenium–Vinylidene Species

Switchable Four- and Five-Component Reactions with Perfect Regioselectivity Promoted by Photoredox/Sulfide Dual-Catalytic Quenching for Access to Diverse Complex Imides

A General Catalytic Sulfide‐based Electron Donor–Acceptor Complex Platform for Decarboxylative Transformations of N‐Hydroxyphthalimide Esters

Photoredox/Sulfide Dual Catalysis for Modular Synthesis of Multi‐substituted Furan Rings via Catalytic Indirect Reductive Quenching

Photoredox catalysis using methoxyarenes: mechanistic studies and synthetic applications

Synthesis of<i>N</i>-(acyloxy)-<i>N</i>-alkynylamides<i>via</i>generation of “C<sub>2</sub>” from hypervalent alkynyliodane and a weak base

A Photoredox/Sulfide Dual Catalysis System That Uses Sulfide Radical Cations to Promote Alkene Chlorotrifluoromethylation

A Catalytic Construction of Indoles via Formation of Ruthenium Vinylidene Species from N‐Arylynamides

Collaborators (3)

kakeru matsukuma

Masanori Tayu

Masahiro Noji

Make your next move.

Aminoalkylation of Alkenes for Modular Pyrrolidine Synthesis <i>via</i> Electron Donor–Acceptor Complexes Generated from Alkenes and Amine-Tethered <i>N</i>-Hydroxyphthalimide Esters

Catalytic Synthesis of Azepinoindoles from Ynamides Containing Indolyl Moieties <i>via</i> Ruthenium–Vinylidene Species