Abstract
Arylidene 2,5-dimethylacetophenones (1) reacted with thiourea and hydrogen peroxide to give pyrimidinethione (2) and oxirane derivatives (7), respectively. The behaviour of pyrimidinethione (2) towards hydrazine, acetylhydrazines, secondary amines under Michael reaction conditions, and phenylisocyanate has been investigated. The reaction of oxirane derivative (7) with aqueous sodium hydroxide, glacial acetic acid and p-xylene under Friedel Crafts reaction conditions is also described
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
