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ChemInform Abstract: Maleimide as an Efficient Nucleophilic Partner in the Aza‐Morita—Baylis—Hillman Reaction: Synthesis of Chiral 3‐Substituted‐3‐aminooxindoles. Issue 39 (September 2015)
Record Type:
Journal Article
Title:
ChemInform Abstract: Maleimide as an Efficient Nucleophilic Partner in the Aza‐Morita—Baylis—Hillman Reaction: Synthesis of Chiral 3‐Substituted‐3‐aminooxindoles. Issue 39 (September 2015)
Main Title:
ChemInform Abstract: Maleimide as an Efficient Nucleophilic Partner in the Aza‐Morita—Baylis—Hillman Reaction: Synthesis of Chiral 3‐Substituted‐3‐aminooxindoles.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>An organocatalytic enantioselective Aza‐Morita—Baylis—Hillman Reaction of maleimide derivatives with various N‐substituted isatin imine derivatives by employing chiral β‐isocupreidine as a catalyst is developed.</p> </abstract>