Abstract
Pyridines are ubiquitous N-heterocycles that are present in many natural products and synthetic drugs with important biological applications. Introduction into a pyridine of a methyl (Me) or an isotopically labeled methyl group at carbon can alter its biological properties. However, regioselective introduction of a Me group in high yield, and preferably in a green manner, is often quite challenging. In this mini-review, several methods, most of which are recent, are examined whereby a Me or CD3 is introduced at a specific carbon in pyridines, as well as in some quinolines.
| Original language | English |
|---|---|
| Pages (from-to) | 766-813 |
| Number of pages | 48 |
| Journal | Heterocycles |
| Volume | 99 |
| Issue number | 2 |
| DOIs | |
| State | Published - 2019 |
Bibliographical note
Publisher Copyright:© 2019 The Japan Institute of Heterocyclic Chemistry.
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