Eduardo Cortés Cortés

TL;DR: In this paper, it was 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.

TL;DR: In this paper, the reaction of β-naphthylamine, dimedone and the appropriate aromatic aldehyde in ethanol gave 1,2,3,4,5,6-hexahydro-2,2-dimethyl-5-aryl-6-aza-9,10-benzophenanthren-4-ones, III, which upon treatement with chromic anhydride, yielded the corresponding tetrahydro derivatives, IV.

TL;DR: An efficient synthesis of four steps to obtain twelve new derivatives of 3,3-dimethyl-2,3,4,5,10,11-hexahydro-8]-(o-; and p-methoxy)phenoxy]-11-[(o,; andp-R)phenyl]-1H-dibenzo[b,e][1,4]diazepin-1-ones IV, 1-12 with possible biological and pharmacological activity as anticonvulsant and schizophrenia treatment in the central nervous system (C

TL;DR: In this article, the preparation of eleven novel 6,7-dimethoxy-1-[(ortho, and para-R)-phenyl]-3,4-dihydroisoquinolines with possible pharmacological activity is described.

TL;DR: In this article, triazolo-1,5-benzodiazepinones III with sodium hydride in methyl iodide gave a mixture of products from which were isolated two compounds IV and V. The structure of all products was confirmed by ir, 1H nmr and mass spectrometry.