Heteroring Annulated Benzimidazolinone Condensed Azepinone Derivatives: A New Class of Highly Potent Antioxidants-Reference-Cited by-同舟云学术

Heteroring Annulated Benzimidazolinone Condensed Azepinone Derivatives: A New Class of Highly Potent Antioxidants

Published:2014-07-20 Issue: Volume:2014 Page:1-5
ISSN:2356-6612
Container-title:Advances in Chemistry
language:en
Short-container-title:Advances in Chemistry

Author:

Garg Neha¹,Jain Priyanka¹,Kishore D.¹

Affiliation:

1. Department of Chemistry, Banasthali University, Banasthali, Rajasthan 304022, India

Abstract

A new class of benzimidazolinone condensed azepinone derivatives annulated on its face “d” with pyrazole, isoxazole, pyrimidine, benzodiazepine, and benzothiazepine nucleus in 3–8, respectively, have been evaluated for their antioxidant activity by DPPH method. Results indicate these to belong to a novel class of highly potent antioxidant agents.

Publisher

Hindawi Limited

Link

http://downloads.hindawi.com/archive/2014/961076.pdf

Reference9 articles.

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2. An approach to regioselective synthesis of pyrazole and isoxazole derivatives and study of their antimicrobial effect

3. Application of chalcones in heterocycles synthesis: Synthesis of 2-(isoxazolo, pyrazolo and pyrimido) substituted analogues of 1,4-benzodiazepin-5-carboxamides linked through an oxyphenyl bridge

4. Expedient Protocols for the Installation of Pyrimidine Based Privileged Templates on 2-Position of Pyrrolo[2,1-c][1,4]-benzodiazepine Nucleus Linked Through a p-phenoxyl Spacer

5. Hard and soft electrophilic and nucleophilic dissymmetry of α-oxoketenedithioacetals and p-nitro-o-phenylenediamine exploited to achieve the regioselectivity in the synthesis of 2-thiomethyl ether substituted isomer of the privileged nucleus of 1,5-benzodiazepines over to its 4-substituted isomers