The Effect of Aryl Substituents in Some Spiro[2‐oxo‐4, 6‐bis (aryl)hexahydropyrimidine‐5,5′‐barbituric acids]

Archiv der Pharmazie

Volumn 322, Issue 4, 1989, Pages 231-235

  Mokrosz, Jerzy L ^a   Paluchowska, Maria H ^a   Szneler, Edward ^b   Drozdz, Barbara ^a  

^a JAGIELLONIAN UNIVERSITY MEDICAL COLLEGE   (Poland)

^b JAGIELLONIAN UNIVERSITY   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

SPIRO[HEXAHYDRO 4,6 DIPHENYL 2 PYRIMIDINONE 5,5' BARBITURIC ACID] DERIVATIVE; UNCLASSIFIED DRUG;

DRUG STRUCTURE; MASS SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE;

EID: 0024560217     PISSN: 03656233     EISSN: 15214184     Source Type: Journal    
DOI: 10.1002/ardp.19893220408     Document Type: Article

References (18)

1. Hydrolysis of barbituric acid derivatives. Part 6. Hydrolysis of spirocyclopropane- and spiro-2?-methylcyclopropane-1?,5-barbituric acids
2. Ortho effects in organic molecules on electron impact. VIII. Intramolecular aromatic substitution in (arylmethylene)barbituric acids.