摘要
Pyridin-2-ylmethyl tosylate derivatives are obtained in high yields from 2-alkylpyridine 1-oxides via a [3,3]-sigmatropic rearrangement of the adduct between 2-alkylpridine 1-oxides with benzenesulfonyl chlorides. Moreover, alkylnitrones also undergo [3,3]-sigmatropic rearrangement to give α-tosylated ketones after hydrolysis. Substitution reactions with nucleophiles then lead to diverse useful functionalizations for the synthesis of pincer ligands.
源语言 | 英语 |
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页(从-至) | 4954-4957 |
页数 | 4 |
期刊 | Organic and Biomolecular Chemistry |
卷 | 16 |
期 | 27 |
DOI | |
出版状态 | 已出版 - 2018 |
已对外发布 | 是 |