4.7 Article

Hydropyridylation of α,β-Unsaturated Esters through Electroreduction of 4-Cyanopyridine

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 87, Issue 8, Pages 5328-5338

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.2c00177

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Funding

  1. National Natural Science Foundation of China [22071067, 21672074]

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A mild and highly efficient method for the hydropyridylation of alpha,beta-unsaturated esters has been developed. This protocol provides the products smoothly with a wide substrate scope in an undivided cell under ambient conditions. Moreover, studies showed that the scope could be extended to other unsaturated compounds, including enones and aldehydes.
A mild and highly efficient method for the hydropyridylation of alpha,beta-unsaturated esters has been developed. This protocol provides the products smoothly with a wide substrate scope in an undivided cell under ambient conditions. Moreover, studies showed that the scope could be extended to other unsaturated compounds, including enones and aldehydes

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