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ChemInform Abstract: p‐Nitrophenyl Ethylthioester in Enantioselective Organocatalytic Michael Additions: Different Behavior of β‐Aryl and β‐Alkyl Enals. Issue 13 (1st April 2014)
Record Type:
Journal Article
Title:
ChemInform Abstract: p‐Nitrophenyl Ethylthioester in Enantioselective Organocatalytic Michael Additions: Different Behavior of β‐Aryl and β‐Alkyl Enals. Issue 13 (1st April 2014)
Main Title:
ChemInform Abstract: p‐Nitrophenyl Ethylthioester in Enantioselective Organocatalytic Michael Additions: Different Behavior of β‐Aryl and β‐Alkyl Enals.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The differences in the reactivity of the thioesters (I) with β‐alkyl and β‐aryl‐substituted enals (II) are overcome by optimization allowing the synthesis of diastereomeric mixtures of Michael adducts (III) and (IV).</p> </abstract>