Issue 36, 2020

3-Aminooxetanes: versatile 1,3-amphoteric molecules for intermolecular annulation reactions

Abstract

Despite the versatility of amphoteric molecules, stable and easily accessible ones are still limitedly known. As a result, the discovery of new amphoteric reactivity remains highly desirable. Herein we introduce 3-aminooxetanes as a new family of stable and readily available 1,3-amphoteric molecules and systematically demonstrated their amphoteric reactivity toward polarized π-systems in a diverse range of intermolecular [3 + 2] annulations. These reactions not only enrich the reactivity of oxetanes, but also provide convergent access to valuable heterocycles.

Graphical abstract: 3-Aminooxetanes: versatile 1,3-amphoteric molecules for intermolecular annulation reactions

Supplementary files

Article information

Article type
Edge Article
Submitted
04 Aug 2020
Accepted
28 Aug 2020
First published
08 Sep 2020
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2020,11, 9945-9949

3-Aminooxetanes: versatile 1,3-amphoteric molecules for intermolecular annulation reactions

Z. Lai, R. Zhang, Q. Feng and J. Sun, Chem. Sci., 2020, 11, 9945 DOI: 10.1039/D0SC04254D

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