作者:Lenka Rodriguez、Roman Fišera、Barbora Gaálová、Kamila Koči、Helena Bujdáková、Mária Mečiarová、Renáta Górová、Helena Jurdáková、Radovan Šebesta
DOI:10.1002/ejoc.202000235
日期:2020.5.10
Organocatalytic Michael addition of aldehydes to nitroalkenes followed by reductive cyclization afford chiral 3,4‐disubstituted pyrrolidines, which are active against methicillin‐resistant strains of Escherichia coli and Staphylococcus aureus.
醛在硝基烯烃上的有机催化迈克尔加成反应,然后进行还原环化,得到手性3,4-二取代的吡咯烷,它们对耐甲氧西林的大肠埃希菌和金黄色葡萄球菌具有活性。