Issue 38, 2022, Issue in Progress

Gold-catalyzed synthesis of oxazoles from alkynyl triazenes and dioxazoles

Abstract

A gold-catalyzed regioselective [3 + 2] cycloaddition of alkynyl triazenes with 1,2,4-dioxazoles was developed. The triazene group in the products could be replaced to obtain iodo-oxazoles, providing potential transformations to diverse oxazole structures. This protocol features readily available starting materials, mild reaction conditions and scalability. A plausible mechanism involving a nitrene transfer process was proposed.

Graphical abstract: Gold-catalyzed synthesis of oxazoles from alkynyl triazenes and dioxazoles

Supplementary files

Article information

Article type
Paper
Submitted
22 Jul 2022
Accepted
25 Aug 2022
First published
31 Aug 2022
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2022,12, 24857-24860

Gold-catalyzed synthesis of oxazoles from alkynyl triazenes and dioxazoles

Z. Mao and H. Zeng, RSC Adv., 2022, 12, 24857 DOI: 10.1039/D2RA04559A

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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