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Issue 2, 2021
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Single point activation of pyridines enables reductive hydroxymethylation

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Abstract

The single point activation of pyridines, using an electron-deficient benzyl group, facilitates the ruthenium-catalysed dearomative functionalisation of a range of electronically diverse pyridine derivatives. This transformation delivers hydroxymethylated piperidines in good yields, allowing rapid access to medicinally relevant small heterocycles. A noteworthy feature of this work is that paraformaldehyde acts as both a hydride donor and an electrophile in the reaction, enabling the use of cheap and readily available feedstock chemicals. Removal of the activating group can be achieved readily, furnishing the free NH compound in only 2 steps. The synthetic utility of the method was illustrated with a synthesis of (±)-Paroxetine.

Graphical abstract: Single point activation of pyridines enables reductive hydroxymethylation

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Article information


Submitted
13 Oct 2020
Accepted
10 Nov 2020
First published
16 Nov 2020

This article is Open Access
All publication charges for this article have been paid for by the Royal Society of Chemistry

Chem. Sci., 2021,12, 742-746
Article type
Edge Article

Single point activation of pyridines enables reductive hydroxymethylation

B. Marinic, H. B. Hepburn, A. Grozavu, M. Dow and T. J. Donohoe, Chem. Sci., 2021, 12, 742 DOI: 10.1039/D0SC05656A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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