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ChemInform Abstract: Catalytic Asymmetric Aminolactonization of 1, 2‐Disubstituted Alkenoic Acid Esters: Efficient Construction of Aminolactones with an All‐Carbon Quaternary Stereo‐Center. Issue 47 (6th November 2014)
Record Type:
Journal Article
Title:
ChemInform Abstract: Catalytic Asymmetric Aminolactonization of 1, 2‐Disubstituted Alkenoic Acid Esters: Efficient Construction of Aminolactones with an All‐Carbon Quaternary Stereo‐Center. Issue 47 (6th November 2014)
Main Title:
ChemInform Abstract: Catalytic Asymmetric Aminolactonization of 1, 2‐Disubstituted Alkenoic Acid Esters: Efficient Construction of Aminolactones with an All‐Carbon Quaternary Stereo‐Center.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The title reaction of alkenoic acid esters gives exclusively trans‐γ and δ‐lactones bearing the amino‐functionality with high enantioselectivities.</p> </abstract>