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ChemInform Abstract: A General, Scalable, Organocatalytic Nitro‐Michael Addition to Enones: Enantioselective Access to All‐Carbon Quaternary Stereocenters. Issue 31 (August 2015)
Record Type:
Journal Article
Title:
ChemInform Abstract: A General, Scalable, Organocatalytic Nitro‐Michael Addition to Enones: Enantioselective Access to All‐Carbon Quaternary Stereocenters. Issue 31 (August 2015)
Main Title:
ChemInform Abstract: A General, Scalable, Organocatalytic Nitro‐Michael Addition to Enones: Enantioselective Access to All‐Carbon Quaternary Stereocenters.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>A tert‐leucine‐derived chiral diamine efficiently catalyzes the asymmetric Michael addition of nitromethane to five, six‐, and seven‐membered β‐substituted cyclic enones furnishing the corresponding adducts with quaternary stereocenter in excellent enantioselectivities.</p> </abstract>