HIGHLIGHTS
- who: jlradomsky from the , Le Mans , France College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science have published the article: Asymmetric Michael addition of acetone to -nitrostyrenes catalyzed by novel organocatalysts derived from D-isomannide or L- isoidide, in the Journal: (JOURNAL)
- what: Although moderate enantioselectivities were observed this study has highlighted that a simple chiral primary diamine can catalyze this reaction. The authors report the preliminary results on asymmetric Michael addition of acetone to trans--nitrostyrenes catalyzed by chiral thioureas and imines organocatalysts derived from D-isomannide- or L-isoidide.
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