TY - JOUR
AU - Toscano, R. Alfredo
AB - It has been reported that dimedone added to α‐arylidennaphthylamines in ethanol with formation of 1,4‐addition products derivatives of 5‐aryl‐5,6,7,8,9,10‐hexahydrobenzo(c)phenanthridin‐7‐ones, III, which are easily oxidized by chromic anhydride to the corresponding tetrahydro derivatives, IV. However, the attempted preparation of these compounds resulted instead of the formation of isomeric acridin‐8‐ones V and VI. Structures were confirmed by ir, 1H nmr, ms and X‐ray spectroscopy.
TI - Synthesis and spectra of 7‐( o ‐ and p‐R ‐phenyl)‐10,10‐dimethyl‐8,9,10,11‐tetrahydrobenz( c )acridin‐8‐ones. Structure correction of 1,2,3,4‐tetrahydro‐2,2‐dimethyl‐5‐aryl‐6‐aza‐7,8‐benzophenanthren‐4‐ones
JF - Journal of Heterocyclic Chemistry
DO - 10.1002/jhet.5570250337
DA - 1988-05-01
UR - https://www.deepdyve.com/lp/wiley/synthesis-and-spectra-of-7-o-and-p-r-phenyl-10-10-dimethyl-8-9-10-11-VPJ4oR6Px0
SP - 895
EP - 899
VL - 25
IS - 3
DP - DeepDyve
ER -