The Mechanism of the Bischler-Napieralski Reaction, II: o-Chlorinated β-Phenethylamides as By-Products of the Ring Closure with PCl5

DOI: 10.1002/ardp.19843170603

Source and publish data:

Archiv der Pharmazie p. 488 - 495 (1984)

Update date:2022-08-02

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Authors:

Berger, Ulrich

Dannhardt, Gerd

Wiegrebe, Wolfgang

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Article abstract of DOI:10.1002/ardp.19843170603

In addition to 3,4-dihydroisoquinolines o-chloro-β-phenethylamides are formed in the Bischler-Napieralski reaction using PCl5.Possible mechanisms for the chlorination were tested in model experiments.

Full text of DOI:10.1002/ardp.19843170603

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