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One-Step Synthesis of Substituted Dihydro- and Tetrahydroisoquinolines by FeCl<sub>3</sub>·6H<sub>2</sub>O Catalyzed Intramolecular Friedel−Crafts Reaction of Benzylamino-Substituted Propargylic Alcohols

87

Citations

22

References

2008

Year

Abstract

A mild, versatile, and efficient method for the one-step synthesis of substituted dihydro- and tetrahydroisoquinolines has been developed by the FeCl3.6H2O catalyzed intramolecular allenylation/cyclization reaction of benzylamino-substituted propargylic alcohols, representing the first example of the intramolecular Friedel-Crafts reaction of propargylic alcohols.

References

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