Thiourea catalysed reduction of α-keto substituted acrylate compounds using Hantzsch ester as a reducing agent in water-Reference-Cited by-同舟云学术

Thiourea catalysed reduction of α-keto substituted acrylate compounds using Hantzsch ester as a reducing agent in water

Published:2017 Issue:37 Volume:7 Page:22909-22912
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Weng Guanglin¹²³⁴,Ma Xiaobo¹²³⁴,Fang Dongmei⁵⁶³⁴,Tan Ping¹²³⁴,Wang Lijiao¹²³⁴,Yang Linlin¹²³⁴,Zhang Yuanyuan¹²³⁴,Qian Shan¹²³⁴,Wang Zhouyu¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Xihua University

3. Chengdu

4. China

5. Chengdu Institute of Biology

6. Chinese Academy of Sciences

Abstract

The first method for the reduction of α-keto substituted acrylate compounds by Hantzsch ester in water under the catalysis of thiourea has been developed. The products were isolated with moderate to high yields (38–95%).

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/RA/C7RA00995J

Reference37 articles.

1. Enantioselective Michael Reaction of α-Alkyl-β-keto Esters and Enones under Multifunctional Catalysis

2. N,N′-Dioxide-Magnesium Ditriflate Complex-Catalyzed Asymmetric α-Hydroxylation of β-Keto Esters and β-Keto Amides

3. A convenient synthesis of tetrazole, precursors of α-dialkylated α-amino acids, by reaction of trimethylsilyl azide with α-dialkylated β-ketoesters

4. Acid Catalyzed Ring Transformation of Benzofurans to Tri- and Tetrasubstituted Furans

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