Masafumi Ueda

Kobe Pharmaceutical University

Japan

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Articles (11)

A diazo-, metal- and additive-free oxime ether synthesis via formal reductive O–H bond insertion of oximes to α-keto esters has been developed.

Year:

2024

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2023

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2023

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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

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2020

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2020

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2020

Collaborators (3)

Motohiro Yasui

Assistant Professor

Kyoto Institute of Technology

JAPAN

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Hiroshi Matsubara

JAPAN

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Takumi Abe

Lecturer

Okayama University

JAPAN

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Masafumi Ueda

Research Interests

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Articles (11)

Synthesis of oxime ethers <i>via</i> a formal reductive O–H bond insertion of oximes to α-keto esters

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

Synthesis of isolable β-chloroenamines from N-alkoxylactams with organometallic reagents

Gold‐Catalyzed Oxyarylation/Hydroxylation of N‐Alkoxypropiolamides for Chemoselective Synthesis of 4‐Aryl‐3‐(2H)‐isoxazolones

Anhydrous Hydrogen Iodide-Mediated Reductive Indolization of In Situ-Generated Cyclopropyl Hydrazones

Construction of pyrazolodiazepines using AuI, a dual functional gold catalyst

Sc(OTf)3-Catalyzed Iodocyclization/Ritter-Type Amidation of N-Alkoxypropiolamides: A Synthetic Strategy for Isoxazol-3(2H)-ones

Synthesis of multi-substituted 1,2,4-triazoles utilising the ambiphilic reactivity of hydrazones

Sequential Nucleophilic Arylation/Ring-Contractive Rearrangement of N-Alkoxylactams

Synthesis of Pyrazoles Utilizing the Ambiphilic Reactivity of Hydrazones

Copper-Catalyzed Sequential Cyclization/Migration of Alkynyl Hydrazides for Construction of Ring-Expanded N–N Fused Pyrazolones

Collaborators (3)

Motohiro Yasui

Hiroshi Matsubara

Takumi Abe

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