Obrecht D., Villalgordo J.M. (1998) Solid-Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compounds Libraries. New York : Pergamon Press 754 832.
Synthesis of the tricyclic portions of batzelladines A, B and D. Revision of the stereochemistry of batzelladines A and D
Snider B.B., Chen J., Patil A.D., Freyer A. (1996) Synthesis of the tricyclic portions of batzelladines A, B and D. Revision of the stereochemistry of batzelladines A and D. Tetrahedron Lett 37 : 6977 6980.
An enantiospecific synthesis of the tricyclic guanidine segment of the anti-HIV marine alkaloid batzelladine A
Rama Rao A.V., Gujar M.K., Vasudevan J. (1995) An enantiospecific synthesis of the tricyclic guanidine segment of the anti-HIV marine alkaloid batzelladine A. J Chem Soc Chem Commun 13 : 1369 1370.
KAl(SO4)2·12H2O supported on silica gel as a novel heterogeneous system catalyzed biginelli reaction: One-pot synthesis of di-hydropyrimidinones under solvent-free conditions
Azizian J., Mohammadi A.A., Karimi A.R., Mohammadizadeh M.R. (2006) KAl(SO4)2·12H2O supported on silica gel as a novel heterogeneous system catalyzed biginelli reaction: one-pot synthesis of di-hydropyrimidinones under solvent-free conditions. Appl Catal A Gen 300 : 85 88.
Biginelli-like three component reaction: Synthesis of some new ethyl 6-ethoxycarbonylmethyl-4-aryl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate derivatives
Azizian J., Mohammadi A.A., Kohshari M., Karimi A.R., Mohammadizadeh M.R. (2007) Biginelli-like three component reaction: synthesis of some new ethyl 6-ethoxycarbonylmethyl-4-aryl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate derivatives. J Heterocycl Chem 44 : 455 458.
Multi-component reaction of amines, alkyl propiolates, and ninhydrin: An efficient protocol for the synthesis of tetrahydro-dihydroxy-oxoindeno[1,2-b] pyrrole derivatives
Azizian J., Hatamjafari F., Karimi A.R., Shaabanzadeh M. (2006) Multi-component reaction of amines, alkyl propiolates, and ninhydrin: an efficient protocol for the synthesis of tetrahydro-dihydroxy-oxoindeno[1,2-b] pyrrole derivatives. Synthesis 5 : 765 767.
Silica sulfuric acid a novel and heterogeneous catalyst for the synthesis of some new oxindole derivatives
Azizian J., Mohammadi A.A., Karimi N., Mohammadizadeh M.R., Karimi A.R. (2006) Silica sulfuric acid a novel and heterogeneous catalyst for the synthesis of some new oxindole derivatives. Catal Commun 7 : 752 755.
Dihydropyridine derivatives to overcome atypical multidrug resistance: Design, synthesis, QSAR studies, and evaluation of their cytotoxic and pharmacological activities
Mehdipour A.R., Javidnia K., Hemmateenejad B., Amirghofran Z., Miri R. (2007) Dihydropyridine derivatives to overcome atypical multidrug resistance: design, synthesis, QSAR studies, and evaluation of their cytotoxic and pharmacological activities. Chem Biol Drug Des 70 : 337 346.
Synthesis, cytotoxicity, QSAR, and intercalation study of new diindenopyridine derivatives
Miri R., Javidnia K., Hemmateenejad B., Azarpira A., Amirghofran Z. (2004) Synthesis, cytotoxicity, QSAR, and intercalation study of new diindenopyridine derivatives. Bioorg Med Chem 12 : 2529 2536.
1,4-Cycloaddition of 1,3-diazabutadienes with enamines: An efficient route to the pyrimidine ring
Barluenga J., Tomas M., Ballesteros A., Lopez L.A. (1989) 1,4-Cycloaddition of 1,3-diazabutadienes with enamines: an efficient route to the pyrimidine ring. Tetrahedron Lett 30 : 4573 4576.
Unprecedented catalytic three component one-pot condensation reaction: An efficient synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin- 2(1H)-ones
Hu E.H., Sidler D.R., Dolling U.H. (1998) Unprecedented catalytic three component one-pot condensation reaction: an efficient synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin- 2(1H)-ones. J Org Chem 63 : 3454 3457.
An expedient protocol of the Biginelli dihydropyrimidine synthesis using carbonyl equivalents
Singh K., Singh J., Deb P.K., Singh H. (1999) An expedient protocol of the Biginelli dihydropyrimidine synthesis using carbonyl equivalents. Tetrahedron 55 : 12873 12880.