摘要
In this study, we present a superacid catalyzed protocol for the α-deuteration of ketones with D2O using [Ph3C]+[B(C6F5)4]− as a pre-catalyst to generate in situ the superacidic species [D]+[B(C6F5)4]−. The features of this catalytic process include simple manipulation, high deuteration efficiency (up to 99%), excellent functional group compatibility and a broad substrate scope, including 30 substrates comprising common building blocks and bioactive molecules like pentoxifylline. Moreover, the avoidance of toxic reagents enables sustainable access to deuterated products, demonstrating the method's practical potential for use in mechanistic studies and pharmaceutical applications.
源语言 | 英语 |
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期刊 | Organic and Biomolecular Chemistry |
DOI | |
出版状态 | 已接受/待刊 - 2025 |
已对外发布 | 是 |