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Dioxane promoted photochemical O-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C–H and C–C bonds
Chemical Communications ( IF 4.9 ) Pub Date : 2024-03-19 , DOI: 10.1039/d4cc00778f
Xinlong Zhou 1 , Jingjing Jiang 1 , Min Zhang 1 , Qingqing Wu 1 , Keyong Zhu 1 , Dongjie Shi 1 , Sensen Hou 1 , Jingjing Zhao 1 , Pan Li 1
Affiliation  

A photochemical synthesis of enol ethers and furan-3(2H)-ones from 1,3-dicarbonyl compounds and aryl diazoacetates has been developed. Significantly, 1,4-dioxane promoted O-alkylation of various 1,3-dicarbonyl compounds beyond previous carbene insertion into C–H and C–C bonds has been disclosed.

中文翻译:

除卡宾插入 C-H 和 C-C 键外,二恶烷促进 1,3-二羰基化合物的光化学 O-烷基化

已经开发出由1,3-二羰基化合物和重氮乙酸芳基酯光化学合成烯醇醚和呋喃-3(2H ) -酮的方法。值得注意的是,1,4-二恶烷促进了各种1,3-二羰基化合物的O-烷基化,超越了之前卡宾插入C-H和C-C键的作用。
更新日期:2024-03-19
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