Facile synthesis of 1,4-benzodiazepine-2,5-diones and quinazolinones from amino acids as anti-tubercular agents-Reference-Cited by-同舟云学术

Facile synthesis of 1,4-benzodiazepine-2,5-diones and quinazolinones from amino acids as anti-tubercular agents

Published:2019 Issue:1 Volume:43 Page:182-187
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Anil Seegehalli M.¹²³⁴⁵,Shobith Rangappa⁶⁷⁵,Kiran Kuppalli. R.¹²³⁴⁵,Swaroop Toreshettahally R.⁸²³⁴⁵,Mallesha Ningegowda⁹⁴⁵,Sadashiva Maralinganadoddi P.¹²³⁴⁵^ORCID

Affiliation:

1. Department of Studies in Chemistry

2. University of Mysore

3. Manasagangothri

4. Mysuru

5. India

6. Adichunchanagiri Institute for Molecular Medicine

7. Nagamangala

8. Department of Studies in Organic chemistry

9. Sri Ram Chem

Abstract

A family of 1,4-benzodiazepine-2,5-diones and quinazolinones with diverse substituents at C-3 position are synthesized by novel, simple and convenient methodology using H₂PtCl₆as catalyst and were all screened for anti-TB activity.

Funder

University Grants Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C8NJ04936J

Reference62 articles.

1. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures

2. Privileged Diazepine Compounds and Their Emergence as Bromodomain Inhibitors

3. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals