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ChemInform Abstract: In(OTf)3‐Catalyzed Synthesis of 2‐Styryl Quinolines: Scope and Limitations of Metal Lewis Acids for Tandem Friedlaender Annulation—Knoevenagel Condensation. Issue 23 (June 2015)
Record Type:
Journal Article
Title:
ChemInform Abstract: In(OTf)3‐Catalyzed Synthesis of 2‐Styryl Quinolines: Scope and Limitations of Metal Lewis Acids for Tandem Friedlaender Annulation—Knoevenagel Condensation. Issue 23 (June 2015)
Main Title:
ChemInform Abstract: In(OTf)3‐Catalyzed Synthesis of 2‐Styryl Quinolines: Scope and Limitations of Metal Lewis Acids for Tandem Friedlaender Annulation—Knoevenagel Condensation.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Among a variety of metal Lewis acids evaluated, In/OTf/<sub>3</sub> is found to be sole catalyst allowing for the synthesis of 2‐styrylguinones (IV)/(17 examples) by a tandem Friedlaender annulation/Knoevenagel condensation sequence.</p> </abstract>