Meerwein arylation reactions of olefins with anthraquinone diazonium hydrogen sulfates: formation f new carbon bonds at the carbon atoms C-1 and at C-1-Reference-Cited by-同舟云学术

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Meerwein arylation reactions of olefins with anthraquinone diazonium hydrogen sulfates: formation f new carbon bonds at the carbon atoms C-1 and at C-1

Published:1988-01 Issue:1 Volume:9 Page:1-20
ISSN:0143-7208
Container-title:Dyes and Pigments
language:en
Short-container-title:Dyes and Pigments

Author:

Weis Claus D.

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,General Chemical Engineering

Reference34 articles.

1. The Development and Synthetic Applications of the Meerwein Reaction

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Blue Light-Emitting Diode-Induced Direct C–H Functionalization of 1,4-Quinones with Aryl and Alkyl Boronic Acids;The Journal of Organic Chemistry;2022-11-02

2. Efficient Processing of Reactions Involving Diazonium Salts: Meerwein Arylation in an Impinging-Jet Reactor;Organic Process Research & Development;2020-07-10

3. Selectivity engineering of Meerwein arylation in a continuous flow reactor: a modelling approach;Reaction Chemistry & Engineering;2020

4. Generation of Arylated Quinones by Iron-Catalyzed Oxidative Arylation of Phenols: Formal Synthesis of Phellodonin, Sarcodonin ε, Leucomelone and Betulinan A;Advanced Synthesis & Catalysis;2014-03-03

5. Practical C−H Functionalization of Quinones with Boronic Acids;Journal of the American Chemical Society;2011-02-22

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