Author:
Nadaraj Vetrivel,Selvi Senniappan Thamarai,Mohan Sellappan,Thangadurai Thangaian Daniel
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics
Reference29 articles.
1. Ambrogi V, Artini D, De Carneri I, Castellino S, Dradi E, Logemann W, Meinardi G, Di Somma M, Tosolini G (1970) Studies on the antibacterial and antifungal properties of 1,4-naphthoquinones. Br J Pharmacol 40:871–880
2. Atwal KS, Swanson BN, Unger SE, Floyd DM, Moreland S, Hedberg A, O’Reilly BC (1991) Dihydropyrimidine calcium channel blockers. 3. 3-Carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agents. J Med Chem 34:806–811
3. Burckhalter JH, Tendick FH, Jones EM, Jones PA, Holcomb WF, Rawlins AL (1948) Aminoalkylphenols as antimalarials. II. (Heterocyclic-amino)-α-amino-o-cresols. The synthesis of camoquin. J Am Chem Soc 70:1363–1373
4. Caddick S (1995) Microwave assisted organic reactions. Tetrahedron 51:10403–10432
5. Daniel Thangadurai T, Ihm SK (2007) Catalytic and antimicrobial studies of ruthenium(III) schiff base complexes containing NS and NNSS donor atoms. Chin J Inorg Chem 23:1515–1522
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