Kim, Sung-Gon published the artcileDiastereoselective organocatalytic Michael addition of 2-arylacetates having an electron-withdrawing group to nitro alkenes, Application In Synthesis of 4230-93-7, the publication is Letters in Organic Chemistry (2012), 9(8), 572-576, database is CAplus.
The first efficient organocatalytic conjugate addition reaction of 2-arylacetates and 2-arylacetonitriles having an electron-withdrawing group to nitro alkenes was achieved using a bifunctional amino thiourea catalyst. The reagents having NO2-, CO2Me-, and CN-functional groups on the aromatic ring can be used; the bifunctional catalyst, N-aminocyclohexyl-N’-bis(trifluoromethyl)phenylthiourea provided Michael adducts in the reaction of various nitro alkenes with broad generality in high yield and diastereoselectivity.
Letters in Organic Chemistry published new progress about 4230-93-7. 4230-93-7 belongs to catalysis-chemistry, auxiliary class Alkenyl,Nitro Compound,Benzene,Ether, name is 1,2-Dimethoxy-4-(2-nitrovinyl)benzene, and the molecular formula is C10H11NO4, Application In Synthesis of 4230-93-7.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia