Copper-catalyzed synthesis of 1,3,5-triarylpentane-1,5-diones from α,β-unsaturated ketones-Reference-Cited by-同舟云学术

Copper-catalyzed synthesis of 1,3,5-triarylpentane-1,5-diones from α,β-unsaturated ketones

Published:2015 Issue:64 Volume:5 Page:52121-52125
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Li Zheng¹²³⁴,Wen Gong¹²³⁴,He Lili¹²³⁴,Li Jiasheng¹²³⁴,Jia Xianggui¹²³⁴,Yang Jingya¹²³⁴

Affiliation:

1. College of Chemistry and Chemical Engineering

2. Northwest Normal University

3. Lanzhou

4. P. R. China

Abstract

An efficient method for copper catalyzed synthesis of 1,3,5-triarylpentane-1,5-diones using α,β-unsaturated ketones as a unique starting material is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA09155A

Reference25 articles.

1. InCl3/Me3SiCl-Catalyzed Direct Michael Addition of Enol Acetates to α,β-Unsaturated Ketones

2. Direct Catalytic Asymmetric Michael Reaction of Hydroxyketones: Asymmetric Zn Catalysis with a Et2Zn/Linked-BINOL Complex

3. The Mukaiyama–Michael addition of a β,β-dimethyl substituted silyl ketene acetal to α,β-unsaturated ketones using tetra-n-butylammonium bibenzoate as a nucleophilic catalyst

4. Magnesium Chloride-Promoted Michael Addition of Dimethylsilyl Enolates to α-Enones

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