2013
DOI: 10.3329/medtoday.v24i2.15012
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Montelukast in Allergic Rhinitis: A Review

Abstract: Abstract

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Cited by 5 publications
(3 citation statements)
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“…The 1 H NMR spectrum of the intermediate (I) are depicted in Fig.3. The 13 C NMR of dial derivative (I) exhibits a sharp peak at 78 ppm with 70% intensity which has been assigned to the methylenic carbons, the sharp peak of weak intensity observed at 192 ppm has been assigned to aldehydic carbon and the medium intensity peaks centered around 112-138 ppm has been attributed to the aromatic carbon atoms pertaining to benzene and naphthalene moieties 25 .…”
Section: Synthesis Of Complexes: General Procedures For the Synthesis mentioning
confidence: 99%
“…The 1 H NMR spectrum of the intermediate (I) are depicted in Fig.3. The 13 C NMR of dial derivative (I) exhibits a sharp peak at 78 ppm with 70% intensity which has been assigned to the methylenic carbons, the sharp peak of weak intensity observed at 192 ppm has been assigned to aldehydic carbon and the medium intensity peaks centered around 112-138 ppm has been attributed to the aromatic carbon atoms pertaining to benzene and naphthalene moieties 25 .…”
Section: Synthesis Of Complexes: General Procedures For the Synthesis mentioning
confidence: 99%
“…These donor atoms coordinate with the metal ion forming dative bonds, modifying its steric and electronic environment as well as its reactivity. [17] Therefore, Schiff bases have a variable denticity, classified according to the number of donor atoms as monodentate, [18] bidentate, [19] tridentate, [20] tetradentate, [21] pentadentate, [22] hexadentate [23] ligands, among others. Schiff bases have gained medical importance for their versatile applications in the treatment of various diseases.…”
Section: Introductionmentioning
confidence: 99%
“…The 1 H NMR spectrum of the intermediate (I)aredepicted in Fig.3. The 13 C NMR of dial derivative (I) exhibits a sharp peak at 78 ppm with 70% intensity which has been assigned to the methylenic carbons, the sharp peak of weak intensity observed at 192 ppm has been assigned to aldehydic carbon and the medium intensity peaks centered around 112-138 ppm has been attributed to the aromatic carbon atoms pertaining to benzene and naphthalene moieties 25 . The 13 C NMR spectrum of the intermediate (I) are depicted in Fig.4 The 1 H NMR spectrum of the ligand (L) exhibits a multiplet around 7.1 ppm to 8.1 ppm assignable to the aromatic protons of Napthaldehyde and benzene groups, the singlet of medium intensity occurring at 9.4 ppm has been assigned to azomethine protons in the macrocycle.…”
Section: Synthesis Of Dialdehydementioning
confidence: 99%