An Accessible Route for the Synthesis of Novel Lignan Derivatives and Their Biological Evaluation


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

2-(Aryl(thiophen-2-yl)methyl)succinic acids (4a – 4d), 3-(aryl(thiophen-2-yl)methyl)dihydrofuran-2,5-diones (5a – 5d), 7-aryl-4-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-6-carboxylic acids (6a – 6d), and ethyl 7-aryl-4-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-6-carboxylates (7a – 7d) were synthesized via Stobbe condensation of aryl(thiophen-2-yl)methanones and diethyl succinate. The newly synthesized compounds (5a – 5d, 6a – 6d, and 7a - 7d) were screened in vitro for their antimicrobial and antioxidant properties. Compounds 5b, 6d, and 7d exhibited promising antifungal and antibacterial activity against various microorganisms tested. Compounds 7d and 7b showed remarkable DPPH radical scavenging abilities.

作者简介

Kanchipura Raghavendra

Department of Studies in Chemistry, University of Mysore, Manasagangothri

Email: ajaykkchem@gmail.com
印度, Mysore

Nagamallu Renuka

Post Graduate Department of Chemistry, Yuvaraja College, University of Mysore

Email: ajaykkchem@gmail.com
印度, Mysore

Kariyappa Kumar

Post Graduate Department of Chemistry, Yuvaraja College, University of Mysore

编辑信件的主要联系方式.
Email: ajaykkchem@gmail.com
印度, Mysore

Sheena Shashikanth

Department of Studies in Chemistry, University of Mysore, Manasagangothri

Email: ajaykkchem@gmail.com
印度, Mysore


版权所有 © Springer Science+Business Media, LLC, part of Springer Nature, 2017
##common.cookie##