Answers are grounded in this paper and cite their sources.
All articles of this category A number of 6,9-disubstituted cyclohepta[ b ]pyrimido[5,4- d ]pyrrole-8(6 H ),10(9 H )-dione derivatives have been synthesized in good to moderate yields by the reaction of 6-amino-3-methyluracil derivatives with 2-chlorotropone in an enamine-alkylation process, subsequent condensation of the amino group with the carbonyl function, dehydrochlorination, and dehydration. cyclohepta[ b ]pyrimido[5,4- d ]pyrrole - 1-azaazulene - 2-chlorotropone - 6-amino-3-methyluracil - enamine-alkylation
No takes yet. Share an insight, caveat, or question.
Nitta et al. (2000) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: