Organic letters

Synthetic Utility of Stannyl Enolates as Radical Alkylating Agents1

K Miura, N Fujisawa, H Saito, D Wang, A Hosomi

文献索引：Miura, Katsukiyo; Fujisawa, Naoki; Saito, Hiroshi; Wang, Di; Hosomi, Akira Organic Letters, 2001 , vol. 3, # 16 p. 2591 - 2594

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被引用次数: 43

摘要

The radical-initiated β-ketoalkylation of haloalkanes with tributylstannyl enolates is described. Stannyl enolates derived from aromatic ketones are reactive toward the homolytic β-ketoalkylation of simple haloalkanes as well as those activated by an electron-withdrawing group. The reactivity of stannyl enolates as radical alkylating agents can be utilized for an efficient three-component coupling reaction among stannyl enolates, haloalkanes, and ...