Ketone C–C Bond Activation Meets the Suzuki-Miyaura Cross-coupling

Xavier Just-Baringo; Igor Larrosa

doi:10.1016/j.chempr.2018.05.012

Ketone C–C Bond Activation Meets the Suzuki-Miyaura Cross-coupling

Xavier Just-Baringo, Igor Larrosa

Research output: Contribution to journal › Short survey › peer-review

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Abstract

In a recent issue of the Journal of the American Chemical Society, Dong and coworkers report that ketones can participate as electrophiles in the Suzuki-Miyaura cross-coupling reaction under Rh(I) catalysis. They show that activation of C–C bonds of unstrained ketones is a versatile process that can engage in cross-coupling reaction with aryl boronates. In a recent issue of the Journal of the American Chemical Society, Dong and coworkers report that ketones can participate as electrophiles in the Suzuki-Miyaura cross-coupling reaction under Rh(I) catalysis. They show that activation of C–C bonds of unstrained ketones is a versatile process that can engage in cross-coupling reaction with aryl boronates.

Original language	English
Pages (from-to)	1203-1204
Number of pages	2
Journal	Chem
Volume	4
Issue number	6
Early online date	14 Jun 2018
DOIs	https://doi.org/10.1016/j.chempr.2018.05.012
Publication status	Published - 14 Jun 2018

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10.1016/j.chempr.2018.05.012

Manuscript 2018-05-16Accepted author manuscript, 410 KBLicence: CC BY-NC-ND

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title = "Ketone C–C Bond Activation Meets the Suzuki-Miyaura Cross-coupling",

abstract = "In a recent issue of the Journal of the American Chemical Society, Dong and coworkers report that ketones can participate as electrophiles in the Suzuki-Miyaura cross-coupling reaction under Rh(I) catalysis. They show that activation of C–C bonds of unstrained ketones is a versatile process that can engage in cross-coupling reaction with aryl boronates. In a recent issue of the Journal of the American Chemical Society, Dong and coworkers report that ketones can participate as electrophiles in the Suzuki-Miyaura cross-coupling reaction under Rh(I) catalysis. They show that activation of C–C bonds of unstrained ketones is a versatile process that can engage in cross-coupling reaction with aryl boronates.",

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AU - Larrosa, Igor

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N2 - In a recent issue of the Journal of the American Chemical Society, Dong and coworkers report that ketones can participate as electrophiles in the Suzuki-Miyaura cross-coupling reaction under Rh(I) catalysis. They show that activation of C–C bonds of unstrained ketones is a versatile process that can engage in cross-coupling reaction with aryl boronates. In a recent issue of the Journal of the American Chemical Society, Dong and coworkers report that ketones can participate as electrophiles in the Suzuki-Miyaura cross-coupling reaction under Rh(I) catalysis. They show that activation of C–C bonds of unstrained ketones is a versatile process that can engage in cross-coupling reaction with aryl boronates.

AB - In a recent issue of the Journal of the American Chemical Society, Dong and coworkers report that ketones can participate as electrophiles in the Suzuki-Miyaura cross-coupling reaction under Rh(I) catalysis. They show that activation of C–C bonds of unstrained ketones is a versatile process that can engage in cross-coupling reaction with aryl boronates. In a recent issue of the Journal of the American Chemical Society, Dong and coworkers report that ketones can participate as electrophiles in the Suzuki-Miyaura cross-coupling reaction under Rh(I) catalysis. They show that activation of C–C bonds of unstrained ketones is a versatile process that can engage in cross-coupling reaction with aryl boronates.

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JO - Chem

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Ketone C–C Bond Activation Meets the Suzuki-Miyaura Cross-coupling

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