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Study of the transformation products of the oxime of 2,7‐dioxo‐3‐methyl‐5‐phenyl‐2,3,5,6‐tetrahydrocyclopenta[ f ]benzoxazole
Author(s) -
Barbry Didier,
Couturier Daniel,
Abdellatifi Noureddine,
Lesieur Daniel,
Lespagnol Charles
Publication year - 1991
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570280246
Subject(s) - chemistry , benzoxazole , beckmann rearrangement , isoquinoline , oxime , derivative (finance) , catalytic hydrogenation , catalysis , medicinal chemistry , stereochemistry , transformation (genetics) , organic chemistry , financial economics , economics , biochemistry , gene
Beckmann rearrangement of the title compound gave only a derivative of an isoquinoline structure and its catalytic hydrogenation afforded the cis isomer of 1‐amino‐3‐phenyl‐1,2‐dihydroindenes.