Issue 24, 2022

Micelle-guided Morita–Baylis–Hillman reaction of ketones in water

Abstract

A novel Morita–Baylis–Hillman reaction employing electron-deficient alkenes like acrylonitrile with a wide range of aryl and aliphatic ketones using cooperative catalysis in micellar media has been delineated. This transformation executed in water under mild reaction conditions in a confined environment of micelles is aligned to the ideas of sustainable and green chemistry. The site of the reaction was established by incisive proton NMR studies in the palisade region of the micellar assembly. This study is expected to encourage the use of micellar catalysis for energetically less favorable chemical reactions.

Graphical abstract: Micelle-guided Morita–Baylis–Hillman reaction of ketones in water

Supplementary files

Article information

Article type
Communication
Submitted
05 Apr 2022
Accepted
23 May 2022
First published
26 May 2022

Org. Biomol. Chem., 2022,20, 4888-4893

Micelle-guided Morita–Baylis–Hillman reaction of ketones in water

M. M. Wani, A. A. Dar and B. A. Bhat, Org. Biomol. Chem., 2022, 20, 4888 DOI: 10.1039/D2OB00638C

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