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ChemInform Abstract: Organocatalytic Enantioselective Synthesis of Tetrahydrofluoren‐9‐ones via Vinylogous Michael Addition/Henry Reaction Cascade of 1, 3‐Indandione‐Derived Pronucleophiles. Issue 27 (16th June 2016)
Record Type:
Journal Article
Title:
ChemInform Abstract: Organocatalytic Enantioselective Synthesis of Tetrahydrofluoren‐9‐ones via Vinylogous Michael Addition/Henry Reaction Cascade of 1, 3‐Indandione‐Derived Pronucleophiles. Issue 27 (16th June 2016)
Main Title:
ChemInform Abstract: Organocatalytic Enantioselective Synthesis of Tetrahydrofluoren‐9‐ones via Vinylogous Michael Addition/Henry Reaction Cascade of 1, 3‐Indandione‐Derived Pronucleophiles.
Abstract: An asymmetric vinylogous Michael addition/Henry cyclization cascade with 1, 3‐indandione derivatives (I), (IV), and (VI) and nitro alkenes affords highly substituted tetrahydrofluorenones.