Issue 15, 2024

Multicomponent synthesis via acceptorless alcohol dehydrogenation: an easy access to tri-substituted pyridines

Abstract

Herein, we report palladium supported on a hydroxyapatite catalyst for synthesizing tri-substituted pyridines using ammonium acetate as the nitrogen source via acceptorless alcohol dehydrogenation strategy. The strategy offers a broad substrate scope using inexpensive and readily available alcohols as the starting material. The catalyst was prepared using a simple method and analyzed by several techniques, including FE-SEM, EDS, HR-TEM, BET, XRD, FT-IR, UV-visible spectroscopy, and XPS, demonstrating the anchoring of Pd nanoparticles on hydroxyapatite in the zero oxidation state. Moreover, several controlled experiments were carried out to understand the reaction pathway and a suitable mechanism has been proposed.

Graphical abstract: Multicomponent synthesis via acceptorless alcohol dehydrogenation: an easy access to tri-substituted pyridines

Supplementary files

Article information

Article type
Paper
Submitted
17 Jan 2024
Accepted
06 Mar 2024
First published
03 Apr 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 10761-10767

Multicomponent synthesis via acceptorless alcohol dehydrogenation: an easy access to tri-substituted pyridines

H. P., V. M. and R. Dey, RSC Adv., 2024, 14, 10761 DOI: 10.1039/D4RA00439F

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