2002
DOI: 10.1016/s0223-5234(02)01355-7
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Mannich bases of 3H-pyrrolo[3,2-f]quinoline having vasorelaxing activity

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Cited by 52 publications
(27 citation statements)
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“…The diazepines, synthesized using our method (Scheme ), have at least two possible centers that are attractive for iminium ions arisen from formaldehyde and an amine interaction: the pyrrole ring and the aromatic one. Both electron‐rich heterocycles such as pyrroles and activated arenes have been reported to undergo aminoalkylation under Mannich conditions.…”
Section: Resultsmentioning
confidence: 99%
“…The diazepines, synthesized using our method (Scheme ), have at least two possible centers that are attractive for iminium ions arisen from formaldehyde and an amine interaction: the pyrrole ring and the aromatic one. Both electron‐rich heterocycles such as pyrroles and activated arenes have been reported to undergo aminoalkylation under Mannich conditions.…”
Section: Resultsmentioning
confidence: 99%
“…Quinoline-based heterocycles have attracted much attention from both synthetic chemists and medicinal chemists due to their interesting anticancer, 1 antimalarial, 2 antibacterial, 3 antimycobacterial, 4 anti-inflammatory, 5 antihypertensive, 6 antiviral, 7 and anti-oxidant activities. 8 Several marketed drugs such as quinine and cabozantinib contain the quinoline scaffold.…”
Section: Introductionmentioning
confidence: 99%
“…Many alkaloids, nucleotides, steroids, peptides, antibiotics and vitamins [6e10] comprise Mannich base fragments. Bioactivity, such as antioxidative [11], antifungal [12], antiinflammatory [13], antimalarial [14], vasorelaxing [15], antitubercular [16], analgesic [17], anticancer [18e21], etc., is a common feature of this class of compounds. Recently, the details on the synthesis and biological activity of some Mannich bases were reported [22].…”
Section: Introductionmentioning
confidence: 99%