The pseudo-michael reaction of 1-aryl-4,5-dihydro-1 h -imidazol- 2-amines with ethyl ethoxymethylenecyanoacetate

HIGHLIGHTS

• who: Annelation Michael addition and colleagues from the Department of Synthesis and Chemical Technology of Medical University of Lublin, A Chodźki St, Lublin, Poland have published the research work: The pseudo-Michael reaction of 1-aryl-4,5-dihydro-1 H -imidazol- 2-amines with ethyl ethoxymethylenecyanoacetate, in the Journal: (JOURNAL)

SUMMARY

Reaction of EMCA with 4,5-dihydro1H-imidazol-2-amines leads to 2,3-dihydroimidaz pyrimidines and represents one of the synthetic methods of this heterocyclic system by reaction of imidazol-2-amine derivatives with electrophilic compounds (the main alternative . . .

 



If you want to have access to all the content you need to log in!

Thanks :)

Username or Email

Password

Remember me

Lost your password?

If you don't have an account, you can create one here.