Issue 8, 2024

Synthesis of enantiopure 1,2,3-triazolylidene-type mesoionic carbene (MIC) conjugate acids featuring a rigid bicyclic scaffold

Abstract

Chiral NHCs have found numerous applications as ligands for transition metals and in their own right for asymmetric catalysis. Here, we report a synthetic route from L-malic acid to enantiopure 1,2,3-triazoliums (mesoionic carbene conjugate acids) with a chiral center in a fused ring.

Graphical abstract: Synthesis of enantiopure 1,2,3-triazolylidene-type mesoionic carbene (MIC) conjugate acids featuring a rigid bicyclic scaffold

Supplementary files

Article information

Article type
Research Article
Submitted
07 Feb 2024
Accepted
19 Feb 2024
First published
20 Feb 2024

Org. Chem. Front., 2024,11, 2178-2181

Synthesis of enantiopure 1,2,3-triazolylidene-type mesoionic carbene (MIC) conjugate acids featuring a rigid bicyclic scaffold

V. Dočekal, M. Melaimi, S. Petrželová, J. Veselý, X. Yan and G. Bertrand, Org. Chem. Front., 2024, 11, 2178 DOI: 10.1039/D4QO00269E

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