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铑催化的非活化末端和内部炔烃的化学和区域选择性的分子间交叉环三聚反应。

Rhodium-Catalyzed Chemo- and Regioselective Intermolecular Cross-Cyclotrimerization of Nonactivated Terminal and Internal Alkynes.

机构信息

Department of Chemical Science and Engineering, Tokyo Institute of Technology , O-okayama, Meguro-ku, Tokyo 152-8550, Japan.

出版信息

J Org Chem. 2017 Oct 20;82(20):11117-11125. doi: 10.1021/acs.joc.7b02121. Epub 2017 Oct 10.

Abstract

It has been established that a cationic rhodium(I)/BIPHEP complex is able to catalyze the unprecedented intermolecular cross-cyclotrimerization of nonactivated terminal and internal alkynes at room temperature. In this transformation, the use of arylacetylenes as terminal alkynes and 1,4-butynediol derivatives as internal alkynes afforded the cross-cyclotrimerization products with good chemo- and regioselectivity. The present study clearly demonstrated that an electronically biased combination of nonactivated and electron-deficient alkynes is not necessary to realize good chemo- and regioselectivity in the cationic rhodium(I) complex-catalyzed intermolecular cross-cyclotrimerization.

摘要

已经确定,一种阳离子铑(I)/BIPHEP 配合物能够在室温下催化非活化末端和内部炔烃的前所未有的分子间交叉环三聚反应。在这种转化中,使用芳基乙炔作为末端炔烃和 1,4-丁炔二醇衍生物作为内部炔烃,以良好的化学和区域选择性得到了交叉环三聚化产物。本研究清楚地表明,在阳离子铑(I)配合物催化的分子间交叉环三聚反应中,实现良好的化学和区域选择性并不一定需要非活化和缺电子炔烃的电子偏向组合。

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