Issue 44, 2021

Reactions involving aryl methyl ketone and molecular iodine: a powerful tool in the one-pot synthesis of heterocycles

Abstract

The preparation of heterocyclic compounds has attracted great attention in organic chemistry because of their extensive application in the field of bioactive molecules, materials science, and natural products. Accordingly, the straightforward design and synthesis of heterocycles using readily accessible starting materials and reagents are among the main targets of synthetic chemists. In this context, reactions involving aryl methyl ketone and molecular iodine are recognized as powerful approaches for one-pot synthesis of heterocyclic compounds. This review focuses on the approaches developed for one-pot synthesis of N,O,S,Se-heterocyclic compounds through reactions involving aryl methyl ketone and molecular iodine over the past ten years.

Graphical abstract: Reactions involving aryl methyl ketone and molecular iodine: a powerful tool in the one-pot synthesis of heterocycles

Article information

Article type
Perspective
Submitted
24 júl 2021
Accepted
14 okt 2021
First published
14 okt 2021

New J. Chem., 2021,45, 20486-20518

Reactions involving aryl methyl ketone and molecular iodine: a powerful tool in the one-pot synthesis of heterocycles

S. Rajai-Daryasarei, M. H. Gohari and N. Mohammadi, New J. Chem., 2021, 45, 20486 DOI: 10.1039/D1NJ03572J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements