Water-mediated decarboxylative radical nitrosation of β-keto acids with <i>tert</i>-butyl nitrite: access to α-oximino ketones-Reference-Cited by-同舟云学术

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Water-mediated decarboxylative radical nitrosation of β-keto acids with tert-butyl nitrite: access to α-oximino ketones

Published:2022 Issue:46 Volume:46 Page:22045-22049
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Jia Lina¹²^ORCID,Li Linlin¹,Han Fuzhong¹²^ORCID,Hu Xiangping³^ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering, Qiqihar University, Qiqihar 161006, China

2. Heilongjiang Provincial Key Laboratory of Catalytic Synthesis for Fine Chemicals, Qiqihar 161006, China

3. Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China

Abstract

A practical catalyst-free decarboxylative radical nitrosation system of β-keto acids with tert-butyl nitrite in water has been described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ04175H

Reference59 articles.

1. Recent Advances in Catalytic Asymmetric Decarboxylative Addition Reactions

2. Catalytic enantioselective decarboxylative reactions using organocatalysts

3. β-Keto Acids in Organic Synthesis

4. Transition metal-free decarboxylative alkylation reactions

5. Catalytic enantioselective decarboxylative nucleophilic addition reactions using chiral organocatalysts

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