Issue 31, 2019

Iodine–DMSO-promoted divergent reactivities of arylacetylenes

Abstract

An unprecedented set of efficient, economical, atom-economic and exceedingly selective I2–DMSO-promoted methods is described for the generation of different structures. The reaction represents the first of its kind, involving the use of different iodine concentrations, temperatures, acids and salt to adjust the selectivity for the synthesis of different alkenes, α-functionalized ketones and α-ketomethylthioesters.

Graphical abstract: Iodine–DMSO-promoted divergent reactivities of arylacetylenes

Supplementary files

Article information

Article type
Communication
Submitted
15 янв 2019
Accepted
07 мар 2019
First published
07 мар 2019

Chem. Commun., 2019,55, 4511-4514

Iodine–DMSO-promoted divergent reactivities of arylacetylenes

S. A. Rather, A. Kumar and Q. N. Ahmed, Chem. Commun., 2019, 55, 4511 DOI: 10.1039/C9CC00346K

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