Iron chloride enhancement of dimethylzinc-mediated radical conjugate addition of ethers and an amine to alkylidenemalonates
摘要:
The addition of FeCl 3 and the use of DMSO as a solvent enabled the radical conjugate addition of a cyclic acetal and a cyclic amine to alkylidenemalonates using a reagent amount (12.5 equiv) of the radical precursors to give Michael addition products in up to 84% yield. This represents a great improvement over the 5% yield obtained under the previously reported conditions.
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DOI:
10.1016/j.tetlet.2009.08.034
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年份:
2009
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来源期刊
Tetrahedron Letters
2009
引用走势
2010
被引量:13
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