化学
立体选择性
钯
烷基化
催化作用
分子内力
亲核细胞
亲核取代
有机化学
基础(拓扑)
药物化学
数学分析
数学
作者
Lingyu Kong,Wenqing Ti,Aijun Lin,Hequan Yao,Yue Huang,Xuanyi Li
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-04-25
卷期号:26 (17): 3591-3596
标识
DOI:10.1021/acs.orglett.4c01045
摘要
A palladium-catalyzed defluorinative alkylation of gem-difluoroalkenes with cyclopropyl alcohols was developed. A range of γ-fluorinated γ,δ-unsaturated ketones were constructed in good yields with excellent stereoselectivities. In addition, by base-mediated intramolecular nucleophilic vinylic substitution (SNV), the products could be further transformed to 2,5-dimethylenetetrahydrofurans and analogues with excellent stereoselectivities.
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