Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 87, Issue 8, Pages 5328-5338Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.2c00177
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Funding
- 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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