One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones
Herein, a direct strategy to synthesize 3-(2-hydroxybenzoyl)-1-aza-anthraquinones with excellent efficiency, mild conditions, and benign functional group compatibility was reported. A variety of 3-formylchromone compounds were employed as compatible substrates and this protocol gave the 3-(2-hydroxy...
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doaj-5706de60694d47b7b22802418cde535c2020-11-25T00:28:02ZengMDPI AGMolecules1420-30492019-08-012416301710.3390/molecules24163017molecules24163017One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinonesJiaqi Yuan0Qian He1Shanshan Song2Xiaofei Zhang3Zehong Miao4Chunhao Yang5State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, ChinaState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, ChinaState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, ChinaState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, ChinaState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, ChinaState Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, ChinaHerein, a direct strategy to synthesize 3-(2-hydroxybenzoyl)-1-aza-anthraquinones with excellent efficiency, mild conditions, and benign functional group compatibility was reported. A variety of 3-formylchromone compounds were employed as compatible substrates and this protocol gave the 3-(2-hydroxybenzoyl)-1-aza-anthraquinone derivatives in good to excellent yields without inert gas and expensive transition metal catalysts. Some compounds displayed good anti-proliferative activities.https://www.mdpi.com/1420-3049/24/16/30173-(2-hydroxybenzoyl)-1-aza-anthraquinoneschromonesanti-proliferation agent |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jiaqi Yuan Qian He Shanshan Song Xiaofei Zhang Zehong Miao Chunhao Yang |
spellingShingle |
Jiaqi Yuan Qian He Shanshan Song Xiaofei Zhang Zehong Miao Chunhao Yang One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones Molecules 3-(2-hydroxybenzoyl)-1-aza-anthraquinones chromones anti-proliferation agent |
author_facet |
Jiaqi Yuan Qian He Shanshan Song Xiaofei Zhang Zehong Miao Chunhao Yang |
author_sort |
Jiaqi Yuan |
title |
One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones |
title_short |
One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones |
title_full |
One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones |
title_fullStr |
One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones |
title_full_unstemmed |
One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones |
title_sort |
one pot and metal-free approach to 3-(2-hydroxybenzoyl)-1-aza-anthraquinones |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2019-08-01 |
description |
Herein, a direct strategy to synthesize 3-(2-hydroxybenzoyl)-1-aza-anthraquinones with excellent efficiency, mild conditions, and benign functional group compatibility was reported. A variety of 3-formylchromone compounds were employed as compatible substrates and this protocol gave the 3-(2-hydroxybenzoyl)-1-aza-anthraquinone derivatives in good to excellent yields without inert gas and expensive transition metal catalysts. Some compounds displayed good anti-proliferative activities. |
topic |
3-(2-hydroxybenzoyl)-1-aza-anthraquinones chromones anti-proliferation agent |
url |
https://www.mdpi.com/1420-3049/24/16/3017 |
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