Catalyst-free facile synthesis of polycyclic indole/pyrrole substituted-1,2,3-triazoles-Reference-Cited by-同舟云学术

Catalyst-free facile synthesis of polycyclic indole/pyrrole substituted-1,2,3-triazoles

Published:2019 Issue:35 Volume:17 Page:8153-8165
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Gour Jitendra¹²³,Gatadi Srikanth¹²³,Akunuri Ravikumar¹²³,Yaddanapudi Madhavi Venkata¹²³,Nengroo Mushtaq Ahmad⁴⁵⁶³,Datta Dipak⁴⁵⁶³,Chopra Sidharth⁷⁸⁶³^ORCID,Nanduri Srinivas¹²³^ORCID

Affiliation:

1. National Institute of Pharmaceutical Education and Research (NIPER)

2. Hyderabad 500 037

3. India

4. Biochemistry Division

5. CSIR-Central Drug Research Institute (CDRI)

6. Lucknow 226031

7. Division of Microbiology

8. CSIR-Central Drug Research Institute

Abstract

A general and catalyst-free access to the fused polycyclic N-heterocycles via an intramolecular azide–alkene cascade reaction under mild reaction conditions has been developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB01560D

Reference82 articles.

1. From Nature to Drug Discovery: The Indole Scaffold as a ‘Privileged Structure’

2. Chemistry and biology of monoterpene indole alkaloid biosynthesis

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5. Design, synthesis and diversification of natural product-inspired hydantoin-fused tetrahydroazepino indoles

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