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1‐Aralkylated Tetrahydro‐2‐benzazepines . Part III. Synthesis from β‐tetralones
Author(s) -
Berney Daniel,
Schuh Karlheinz
Publication year - 1976
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19760590619
Subject(s) - tetralones , chemistry , beckmann rearrangement , benzazepines , stereochemistry , organic chemistry , catalysis
1‐Benzyl‐tetrahydro‐2‐benzazepin‐3‐ones 4 were prepared by submitting the corresponding 1‐benzyl‐β‐tetralones 3 to the Schmidt reaction. On the other hand, the rearrangement of the tetralones 3 by the Beckmann procedure gave 1‐benzyl‐tetrahydro‐3‐benzazepin‐2‐ones 5 . The syntheses of some hexahydrophenanthro‐azepines of types 10 and 15 are also described.
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