Issue 67, 2020

A new entry to highly functionalized pyrroles via a cascade reaction of α-amino esters and alkynals

Abstract

Here, we developed an expedient access route to highly functionalized pyrroles from readily available α-amino acid ester hydrochlorides and alkynals via a cascade condensation/intramolecular cyclization followed by a unique C–N ester migration process. A variety of 1,2,3-trisubstituted pyrroles, which were difficult to acquire with the common methodologies, were successfully prepared in good yields under mild conditions.

Graphical abstract: A new entry to highly functionalized pyrroles via a cascade reaction of α-amino esters and alkynals

Supplementary files

Article information

Article type
Communication
Submitted
24 Apr 2020
Accepted
13 Jul 2020
First published
13 Jul 2020

Chem. Commun., 2020,56, 9691-9694

A new entry to highly functionalized pyrroles via a cascade reaction of α-amino esters and alkynals

L. Wei, S. Xu, Z. Jia, H. Tao and C. Wang, Chem. Commun., 2020, 56, 9691 DOI: 10.1039/D0CC02964E

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