A transition metal-free approach towards synthesis of β-carboline tethered 1,3,4-oxadiazoles via oxidative C–O bond formation-Reference-Cited by-同舟云学术

A transition metal-free approach towards synthesis of β-carboline tethered 1,3,4-oxadiazoles via oxidative C–O bond formation

Published:2019 Issue:1 Volume:43 Page:93-102
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Singh Dharmender¹²³⁴,Tiwari Sandip Kumar⁵⁶⁷⁸⁴,Singh Virender¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Dr B R Ambedkar National Institute of Technology (NIT)

3. Jalandhar

4. India

5. Drug Discovery and Molecular Synthesis Lab

6. Centre of Biomedical Research

7. SGPGIMS

8. Lucknow- 226014

Abstract

An efficient protocol has been developed for one-pot synthesis of biologically interesting β-carboline substituted 1,3,4-oxadiazoles via an I₂-assisted oxidative C–O bond formation strategy.

Funder

Science and Engineering Research Board

Council of Scientific and Industrial Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C8NJ04294B

Reference58 articles.

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4. In Vivo Antimalarial Activity of the Beta-Carboline Alkaloid Manzamine A

5. Synthesis and evaluation of β-carboline derivatives as inhibitors of human immunodeficiency virus

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