Issue 10, 2024

Blue light-mediated carbene transfer reaction of thioesters with diazoesters: efficient synthesis of tetrasubstituted Z-enol esters

Abstract

A novel and efficient metal-free, blue light-mediated carbene transfer reaction of thioesters with diazoesters has been achieved. This protocol produces a variety of tetrasubstituted Z-enol esters containing aryl sulfur groups in good yields under mild, convenient and catalyst-free conditions.

Graphical abstract: Blue light-mediated carbene transfer reaction of thioesters with diazoesters: efficient synthesis of tetrasubstituted Z-enol esters

Supplementary files

Article information

Article type
Research Article
Submitted
06 Feb 2024
Accepted
02 Apr 2024
First published
04 Apr 2024

Org. Chem. Front., 2024,11, 2928-2933

Blue light-mediated carbene transfer reaction of thioesters with diazoesters: efficient synthesis of tetrasubstituted Z-enol esters

S. Wang, H. Zhang, J. Yang, D. Zhang and X. Hui, Org. Chem. Front., 2024, 11, 2928 DOI: 10.1039/D4QO00265B

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