Volume 130, Issue 13 pp. 3502-3506
Zuschrift

Epoxides as Alkylating Reagents for the Catellani Reaction

Dr. Hong-Gang Cheng

Dr. Hong-Gang Cheng

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

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Chenggui Wu

Chenggui Wu

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

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Han Chen

Han Chen

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

These authors contributed equally.

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Ruiming Chen

Ruiming Chen

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

These authors contributed equally.

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Guangyin Qian

Guangyin Qian

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

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Zhi Geng

Zhi Geng

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

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Qiang Wei

Qiang Wei

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

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Yuanyuan Xia

Yuanyuan Xia

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

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Jingyang Zhang

Jingyang Zhang

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

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Yuming Zhang

Yuming Zhang

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

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Prof. Dr. Qianghui Zhou

Corresponding Author

Prof. Dr. Qianghui Zhou

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072 China

The Institute for Advanced Studies, Wuhan University, Wuhan, 430072 China

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First published: 24 January 2018
Citations: 23

Dedicated to Prof. Phil S. Baran and Prof. Dawei Ma

Abstract

We report a cooperative catalytic system comprising a PdII complex, XPhos, and the potassium salt of 5-norbornene-2-carboxylic acid that enables the use of epoxides as alkylating reagents in the Catellani reaction, thereby expanding the existing paradigm of this powerful transformation. The potassium salt of inexpensive 5-norbornene-2-carboxylic acid acts as both mediator and base in the process. This mild, chemoselective, scalable, and atom-economical protocol is compatible with a wide variety of readily available functionalized aryl iodides and epoxides, as well as terminating olefins. The resulting products undergo facile oxa-Michael addition to furnish ubiquitous isochroman scaffolds.

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