An efficient, step-economical synthesis of β-carboline tethered imidazopyrido[3,4-<i>b</i>]indoles from acetals-Reference-Cited by-同舟云学术

An efficient, step-economical synthesis of β-carboline tethered imidazopyrido[3,4-b]indoles from acetals

Published:2024 Issue:25 Volume:48 Page:11394-11406
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Vaishali ¹²^ORCID,Banyal Naveen¹³^ORCID,Sharma Shubham⁴^ORCID,Singh Manpreet⁵,Malakar Chandi C.⁶^ORCID,Singh Virender³

Affiliation:

1. Department of Chemistry, Dr B R Ambedkar National Institute of Technology (NIT), Jalandhar, 144027, Punjab, India

2. Department of Chemistry, BK Birla Institute of Higher Education, Pilani, Rajasthan, 333031, India

3. Department of Chemistry, Central University of Punjab, Bathinda, 151401, Punjab, India

4. Department of Chemistry, GLA University, Mathura, UP, 281406, India

5. Department of Chemistry, Baba Farid Group of Institutions, Bathinda, India

6. Department of Chemistry, NIT Manipur, Imphal, India

Abstract

An efficient one-pot pseudo three component cascade annulation reaction has been devised to generate the fluorescent β-carboline tethered imidazopyrido[3,4-b]indole derivatives.

Funder

Human Resource Development Group

Council of Scientific and Industrial Research, India

Science and Engineering Research Board

University of Central Punjab

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NJ/D4NJ01467G

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