Sequential multicomponent site-selective synthesis of 4-iodo and 5-iodopyrrole-3-carboxaldehydes from a common set of starting materials by tuning the conditions-Reference-Cited by-同舟云学术

Sequential multicomponent site-selective synthesis of 4-iodo and 5-iodopyrrole-3-carboxaldehydes from a common set of starting materials by tuning the conditions

Published:2020 Issue:6 Volume:18 Page:1155-1164
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Choudhary Sachin¹²³⁴^ORCID,Yadav Jyothi¹²³⁴,Mamta ¹²³⁴,Pawar Amol Prakash¹²³⁴,Vanaparthi Satheeshvarma¹²³⁴^ORCID,Mir Nisar A.¹²³⁴,Iype Eldhose⁵⁶⁷⁸,Sharma Ratika⁹¹⁰¹¹¹²⁴,Kant Rajni⁹¹⁰¹¹¹²⁴,Kumar Indresh¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Birla Institute of Technology and Science

3. Pilani 333 031

4. India

5. Department of Chemical Engineering

6. BITS Pilani

7. Dubai

8. United Arab Emirates

9. X-ray Crystallography Laboratory

10. Post-Graduate Department of Physics & Electronics

11. University of Jammu

12. Jammu 180 006

Abstract

A simple and straightforward method for the synthesis of 4-iodo and 5-iodopyrrole-3-carboxaldehydes is developed in good to high yields (up to 78%) from a common set of starting materials by tuning the reaction conditions.

Funder

Birla Institute of Technology and Science, Pilani

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/C9OB02501D

Reference43 articles.

1. Pyrroles , in The Chemistry of Heterocyclic Compounds , ed. R. A. Jones , Wiley , New York , 1990 , vol. 48 , part I

2. Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions