Turkish Journal of Chemistry
DOI
-
Abstract
3,4-Diformyl-2,5-dimethylpyrrole (1) reacts with 1,2-diphenyl-1,2-diamine derivatives to form the potentially tautomeric 2:2 macrocyclic adduct (1)=(1). ^1H and ^{13}C n.m.r. spectral data along with acidity measurements indicate that the 2-azafulvene structure (7) is predominant for all adducts.
First Page
137
Last Page
142
Recommended Citation
ÖĞRETİR, Cemil and SEVERCAN, Fatma (1998) "Reaction of 3,4-Diformyl-2,5-dimethylpyrrole with 1,2(substituted)diphenyl-1,2-diaminoethanes," Turkish Journal of Chemistry: Vol. 22: No. 2, Article 7. Available at: https://journals.tubitak.gov.tr/chem/vol22/iss2/7