Pd-Catalyzed Spirocyclization via C-H Activation and Benzyne Insertion.

Pd-Catalyzed Spirocyclization via C-H Activation and Benzyne Insertion.
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DOI:
10.1021/acs.orglett.6b03213
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发表时间:
2016-12
期刊:
影响因子:
5.2
通讯作者:
H. Yoon;A. Lossouarn;Felicitas Landau;M. Lautens
H. Yoon;A. Lossouarn;Felicitas Landau;M. Lautens
中科院分区:
化学1区
文献类型:
--
作者:
H. Yoon;A. Lossouarn;Felicitas Landau;M. Lautens

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钯催化的螺环化反应生成螺羟吲哚和螺二氢苯并呋喃。机理研究表明,通过连续的碳钯化,C-H活化,和苯炔插入的转化收益。这两类螺环化合物的合成产率都很高,并且该方法易于扩展。
A palladium-catalyzed spirocyclization forming spirooxindoles and spirodihydrobenzofurans has been achieved. Mechanistic studies suggest that the transformation proceeds through sequential carbopalladation, C-H activation, and benzyne insertion. Both classes of spirocycles have been synthesized in good to excellent yields, and the procedure is readily scalable.