32263-20-0Relevant articles and documents
Amidine-Enediamine Tautomerism. A Novel Michael-type Reaction
Pfau, Michel,Chiriacescu, Marina,Revial, Gilbert
, p. 327 - 330 (1993)
Cyclic amidines 4 and 11 have been shown to be in N,C-tautomeric equilibrium with the corresponding ene-1,1-diamines which can be C-alkylated by methyl acrylate, leading respectively to the corresponding functionalized substituted amidines 6 (or 7) and 12.Key-words: amidine-ene-1,1-diamine tautomerism; C-alkylation; Michael-type reaction; α-alkylated cyclic amidines; methyl acrylate