Synthesis and evaluation of some new fluorinated hydroquinazoline derivatives as antifungal agents II
doi:10.1016/S0014-827X(00)00029-X
Abdel-Gawad SM, El-Gaby MSA, Ghorab MM (2000) Synthesis and evaluation of some new fluorinated hydroquinazoline derivatives as antifungal agents II. Farmaco 55(4):249-255. doi:10.1016/S0014-827X(00)00029-X
A revision of the biginelli reaction under solid acid catalysis solvent-free synthesis of dihydropyrimidines over montmorillonite KSF
doi:10.1016/S0040-4039(99)00424-4
Bigi F, Carloni S, Frullanti B, Muggi R, Sartori G (1999) A revision of the biginelli reaction under solid acid catalysis solvent-free synthesis of dihydropyrimidines over montmorillonite KSF. Tetrahedron Lett 40(17):3465-3468. doi:10.1016/S0040-4039(99)00424-4
An efficient and high yielding protocol for the synthesis of substituted dihydropyrimidin-2(1 h)-ones and spiro-fused heterocycles by involving tandem reactions
doi:10.1002/jhet.5570440133
Bose DS, Idrees M (2007) An efficient and high yielding protocol for the synthesis of substituted dihydropyrimidin-2(1 h)-ones and spiro-fused heterocycles by involving tandem reactions. J Heterocyclic Chem 44(1):211-214. doi:10.1002/jhet.5570440133
One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-(thio)ones using strontium(II) nitrate as a catalyst
doi:10.1016/j.molcata.2006.07.037
Chenjiang L, Wang J, Yanping L (2006) One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-(thio)ones using strontium(II) nitrate as a catalyst. J Mol Catal A 258(1-2):367-370. doi:10.1016/j.molcata.2006.07.037
(2006)J Mol Catal A, vol.258, Issue.1-2, pp. 367-370
An efficient and clean one-pot synthesis of 3,4-dihydropyrimidine-2(1H)- ones catalyzed by tungstate sulfuric acid in solvent-free conditions
doi:10.1002/jhet.5570450438
Esfahani MN, Karami B, Montazerozohori M, Abdi K (2008) An efficient and clean one-pot synthesis of 3,4-dihydropyrimidine-2(1H)-ones catalyzed by tungstate sulfuric acid in solvent-free conditions. J Heterocyclic Chem 45(4):1183-1185. doi:10.1002/jhet.5570450438
Researches on pyrimidines. CXXXVI. The mechanism of formation of tetrahydropyrimidines by the biginelli reaction
doi:10.1021/ja01336a054
Folkers K, Johnson TB (1933) Researches on pyrimidines. CXXXVI. The mechanism of formation of tetrahydropyrimidines by the biginelli reaction. J Am Chem Soc 55(9):3784-3791. doi:10.1021/ja01336a054
Hydrogenation of cyclic ureides under elevated temperatures and pressures. I1 2-keto-1,2,3,4-tetrahydropyrimidines
doi:10.1021/ja01320a058
Folkers K, Johnson TB (1934) Hydrogenation of cyclic ureides under elevated temperatures and pressures. I1 2-keto-1,2,3,4-tetrahydropyrimidines. J Am Chem Soc 56(5):1180-1185. doi:10.1021/ja01320a058
Researches on pyrimidines. Cxxx. Synthesis of 2-keto-1,2,3,4- tetrahydropyrimidines
doi:10.1021/ja01348a040
Folkers K, Harwood HJ, Johnson TB (1932) Researches on pyrimidines. Cxxx. Synthesis of 2-keto-1,2,3,4-tetrahydropyrimidines. J Am Chem Soc 54(9):3751-3758. doi:10.1021/ja01348a040
A novel approach for mannich-type bases having a terminal olefin: Zinc triflate and water-promoted cyclization/C-N bond cleavage process
doi:10.1021/jo0011888
Ishimaru K, Kojima T (2000) A novel approach for mannich-type bases having a terminal olefin: zinc triflate and water-promoted cyclization/C-N bond cleavage process. J Org Chem 65(24): 8395-8398. doi:10.1021/jo0011888
A reexamination of the mechanism of the biginelli dihydropyrimidine synthesis. Support for an N-acyliminium ion intermediate
doi:10.1021/jo971010u
Kappe CO (1997) A reexamination of the mechanism of the biginelli dihydropyrimidine synthesis. Support for an N-acyliminium ion intermediate. J Org Chem 62(21):7201-7204. doi:10.1021/jo971010u
Biologically active dihydropyrimidones of the biginelli-type - A literature survey
doi:10.1016/S0223-5234(00)01189-2
Kappe CO (2000) Biologically active dihydropyrimidones of the biginelli-type-a literature survey. Eur J Med Chem 35(12): 1043-1052. doi:10.1016/S0223-5234(00)01189-2
Synthesis of 4-aryl-7,7-dimethyl-1,2,3,4,5,6,7,8-octahydroquinazoline-2- one/thione-5-one derivatives and evaluation as antibacterials
doi:10.1016/j.ejmech.2005.02.009
Kidwai M, Saxena S, Khan MKR, Thukral SS (2005) Synthesis of 4-aryl-7,7-dimethyl-1,2,3,4,5,6,7,8-octahydroquinazoline-2-one/thione-5-one derivatives and evaluation as antibacterials. Eur J Med Chem 40(8):816-819. doi:10.1016/j.ejmech.2005.02.009
An efficient three component one-pot synthesis of some new octahydroquinazolinone derivatives and investigation of their antimicrobial activities
Ladani NK, Patel MP, Patel RG (2009) An efficient three component one-pot synthesis of some new octahydroquinazolinone derivatives and investigation of their antimicrobial activities. Arkivoc vii:292-302
Nafion-H catalyzed cyclocondensation reaction for the synthesis of octahydroquinazolinone derivatives
doi:10.1016/j.molcata.2006.12.020
Lin H, Zhao Q, Xu B, Wang X (2007) Nafion-H catalyzed cyclocondensation reaction for the synthesis of octahydroquinazolinone derivatives. J Mol Catal 268(1-2):221-226. doi:10.1016/j.molcata.2006.12.020
(2007)J Mol Catal, vol.268, Issue.1-2, pp. 221-226
Microwave assisted synthesis of some novel thiopyrano[2, 3-b]quinolines as a new class of antimicrobial agent
doi:10.1080/10426500500366285
Nandeshwarappa B, Aruna Kumar DB, Kumaraswamy MN, Ravikumar YS, Bhojya Naik H, Mahadevan KM (2006) Microwave assisted synthesis of some novel thiopyrano[2, 3-b]quinolines as a new class of antimicrobial agent. Phosphorus Sulfur Silicon 181(7):1545-1556. doi:10.1080/10426500500366285
National Committee for Clinical Laboratory Standards (NCCLS) West Valley Road, Suite 1400, Wayne, Pennsylvania 19087-1898, USA; Twelfth Informational Supplement ISBN 1-56238-454-6,M100-S12 (M7)
National Committee for Clinical Laboratory Standards (NCCLS) (2002) West Valley Road, Suite 1400, Wayne, Pennsylvania 19087-1898, USA. Performance Standards for Antimicrobial Susceptibility Testing; Twelfth Informational Supplement ISBN 1-56238-454-6,M100-S12 (M7)
Synthesis, characterization and anti-bacterial activity of some new 2,3,6-trisubstituted quinazolin-4(3H)-ones
Patel RD, Patel MP, Patel RG (2005) Synthesis, characterization and anti-bacterial activity of some new 2,3,6-trisubstituted quinazolin-4(3H)-ones. Indian J Chem 44B(9):1944-1946
(2005)Indian J Chem, vol.44 B, Issue.9, pp. 1944-1946
Synthesis of the tricyclic portions of batzelladines A, B and D. Revision of the stereochemistry of batzelladines A and D
doi:10.1016/0040-4039(96)01575-4
Sinder B, Chen J, Patil AD, 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(39): 6977-6980. doi:10.1016/0040- 4039(96)01575-4
Biomimetic synthesis of (.+-.)-crambines A, B, C1, and C2. Revision of the structure of crambines B and C1
doi:10.1021/jo00067a014
Snider BB, Shi Z (1993) Biomimetic synthesis of (.+-.)-crambines A, B, C1, and C2. Revision of the structure of crambines B and C1. J Org Chem 58(15):3828-3839. doi:10.1021/jo00067a014
Vilsmeier-Haack reagent: A facile synthesis of 2-chloro-3- formylquinolines from N-arylacetamides and transformation into different functionalities
Sriyastava A, Singh RM (2005) Vilsmeier-Haack reagent: a facile synthesis of 2-chloro-3-formylquinolines from N-arylacetamides and transformation into different functionalities. Indian J Chem 44B(9):1868-1875
(2005)Indian J Chem, vol.44 B, Issue.9, pp. 1868-1875
A solid phase protocol of the biginelli dihydropyrimidine synthesis suitable for combinatorial chemistry
doi:10.1016/0040-4039(95)01660-A
Wipf P, Cunningham A (1995) A solid phase protocol of the biginelli dihydropyrimidine synthesis suitable for combinatorial chemistry. Tetrahedron Lett 36(43):7819-7822. doi:10.1016/0040-4039(95)01660-A
One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones using chloroacetic acid as catalyst
doi:10.1016/j.bmcl.2006.12.068
Yang Y, Liu D, Liu C, Luo G (2007) One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones using chloroacetic acid as catalyst. Bioorg Med Chem Lett 17(12):3508-3510. doi:10.1016/j.bmcl.2006.12.068
Synthesis and in vitro calcium antagonist activity of 4-aryl-7,7-dimethyl/1,7,7-trimethyl-1,2,3,4,5,6,7,8-octahydroquinazoline-2, 5-dione derivatives
doi:10.1016/S0014-827X(02)00009-5
Yarim M, Sarac S, Kilic FS, Erol K (2003) Synthesis and in vitro calcium antagonist activity of 4-aryl-7,7-dimethyl/1,7,7-trimethyl-1,2,3,4,5,6,7,8- octahydroquinazoline-2,5-dione derivatives. II Farmaco 58(1):17-24. doi:10.1016/S0014-827X(02)00009-5
Multi-component synthesis of dihydropyrimidines by iodine catalyst at ambient temperature and in vitro antimycobacterial activity
doi:10.1002/ardp.200800224
Zalavadiya P, Tala S, Akbari J, Joshi H (2009) Multi-component synthesis of dihydropyrimidines by iodine catalyst at ambient temperature and in vitro antimycobacterial activity. Arch Pharm Chem Life Sci 342(8):469-475. doi:10.1002/ardp.200800224