Issue 16, 2021, Issue in Progress

Monoallylation and benzylation of dicarbonyl compounds with alcohols catalysed by a cationic cobalt(iii) compound

Abstract

Monoallylation and monoalkylation of diketones and β-keto esters with allylic and benzylic alcohols catalysed by [Cp*Co(CH3CN)3][SbF6]2 (I) are reported. The method does not require any additive and affords regioselective products. The mechanistic investigations were done by in situ 1H NMR spectroscopy as well as control experiments. It has been shown that reactions proceed via η3-allyl complex formation or ally ether intermediate. The alkylation takes place via only ether intermediate. The resulting allylated and alkylated products have been used for the synthesis of eleven new trisubstituted pyrazoles and one pyrazolone.

Graphical abstract: Monoallylation and benzylation of dicarbonyl compounds with alcohols catalysed by a cationic cobalt(iii) compound

Supplementary files

Article information

Article type
Paper
Submitted
18 Nov 2020
Accepted
19 Feb 2021
First published
01 Mar 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 9235-9245

Monoallylation and benzylation of dicarbonyl compounds with alcohols catalysed by a cationic cobalt(III) compound

M. Chandra Sau, S. Mandal and M. Bhattacharjee, RSC Adv., 2021, 11, 9235 DOI: 10.1039/D0RA09778K

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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