Abstract
1,3-Diaryl-2-propene-1-ones react with ethyl cyanoacetate in presence of sodium ethoxide at room temperature to give 2-aroyl-1,3,5-triaryl-4-carbethoxy-4-cyanocyclohexanols. The structure of the reaction products was established by infrared, H-1 and C-13 nuclear magnetic resonance spectral data as well as elemental analysis. X-ray crystallography shows the presence of the cyclohexanol moeity.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
