An efficient one pot synthesis of 2-amino quinazolin-4(3H)-one derivative via MCR strategy
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[1] C. Cai,et al. One-pot synthesis of 2-amino-4(3H)-quinazolinones via ring-opening of isatoic anhydride and palladium-catalyzed oxidative isocyanide-insertion. , 2014, Organic & biomolecular chemistry.
[2] Jianghua He,et al. Synthesis of 2‐Amino 3‐Substituted Quinazolin‐4(3H)‐one Derivatives via Iodine‐Mediated Guanidinylation of Pbf‐Activated Thiourea , 2013 .
[3] Hanmant Gaikwad,et al. TBAHS-Catalyzed Synthesis of 2-Dihydroquinazolin-2-ylquinoline: An Efficient and Practical Synthesis of Naturally Occurring Alkaloids Luotonin A, B, and E , 2012 .
[4] Jaulang Hwang,et al. One-pot synthesis of luotonin A and its analogues. , 2011, Organic letters.
[5] M. Takacs,et al. Synthesis of hybrids between the alkaloids rutaecarpine and luotonins A, B , 2008 .
[6] S. Chierici,et al. Concise synthesis of 2-amino-4(3H)-quinazolinones from simple (Hetero)aromatic amines. , 2008, The Journal of organic chemistry.
[7] P. Knochel,et al. Relative Geschwindigkeiten der Brom-Magnesium-Austauschreaktionen an substituierten Brombenzolderivaten† , 2008 .
[8] M. Elsegood,et al. Radical reactions with 3H-quinazolin-4-ones: synthesis of deoxyvasicinone, mackinazolinone, luotonin A, rutaecarpine and tryptanthrin. , 2007, Organic & biomolecular chemistry.
[9] P. Knochel,et al. Hocheffiziente Reagentien für den Brom-Magnesium-Austausch† , 2006 .
[10] M. Iranshahi,et al. Improved Synthesis of Vasicinone , 2004 .
[11] S. P. Chavan,et al. A short and efficient general synthesis of luotonin A, B and E , 2004 .
[12] A. Kamal,et al. One pot conversion of azido arenes to N-arylacetamides and N-arylformamides: synthesis of 1,4-benzodiazepine-2,5-diones and fused [2,1-b]quinazolinones , 2004 .
[13] N. Argade,et al. Regioselective quinazolinone-directed ortho lithiation of quinazolinoylquinoline: practical synthesis of naturally occurring human DNA topoisomerase I poison luotonin a and luotonins B and E. , 2004, The Journal of organic chemistry.
[14] N. Argade,et al. Facile zeolite induced Fischer-indole synthesis: a new approach to bioactive natural product rutaecarpine , 2004 .
[15] T. Nomura,et al. Novel quinazoline-quinoline alkaloids with cytotoxic and DNA topoisomerase II inhibitory activities. , 2004, Bioorganic & medicinal chemistry letters.
[16] K. Shikhaliev,et al. Condensation of Isatoic Anhydride with Hetarylguanidines , 2003 .
[17] H. Abe,et al. A Convenient Synthesis of Luotonins A and B , 2003 .
[18] B. Kundu,et al. Solid-phase synthesis of quinazolin-4(3H)-ones with three-point diversity☆ , 2002 .
[19] R. Houghten,et al. A traceless approach for the parallel solid-phase synthesis of 2-(arylamino)quinazolinones. , 2002, The Journal of organic chemistry.
[20] H. Tokuda,et al. Studies on the chemical transformations of rotenoids. 6 Synthesis and antitumor-promoting activity of† benzofuro[2,3-d]pyridazines fused with 1,2,4-triazole, 1,2,4-triazine and 1,2,4-triazepine , 2001 .
[21] M. Shvekhgeimer. Synthesis of Heterocyclic Compounds Based on Isatoic Anhydrides (2H-3,1-Benzoxazine-2,4-diones). (Review) , 2001 .
[22] A. Kamal,et al. Chemoenzymatic synthesis of pyrrolo[2,1-b]quinazolinones: lipase-catalyzed resolution of vasicinone. , 2001, The Journal of organic chemistry.
[23] Rui Yang,et al. A concise and efficient solid-phase synthesis of 2-amino-4(3H)-quinazolinones , 2000 .
[24] A. Gopalsamy,et al. Combinatorial synthesis of heterocycles: solid-phase synthesis of 2-amino-4(1H)-quinazolinone derivatives. , 2000, Journal of combinatorial chemistry.
[25] D. Sriram,et al. Synthesis, antibacterial, antifungal and anti-HIV evaluation of Schiff and Mannich bases of isatin derivatives with 3-amino-2-methylmercapto quinazolin-4(3H)-one. , 1999, Pharmaceutica acta Helvetiae.
[26] N. A. Santagati,et al. 4-quinazolinones: synthesis and reduction of prostaglandin E2 production. , 1999, Farmaco.
[27] J Ramis,et al. New azole antifungals. 3. Synthesis and antifungal activity of 3-substituted-4(3H)-quinazolinones. , 1998, Journal of medicinal chemistry.
[28] A. Bell,et al. Novel antifungal 2-aryl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol derivatives with high activity against Aspergillus fumigatus , 1996 .
[29] N. Leonard,et al. Convenient synthesis of linear benzopurines through a common intermediate , 1987 .
[30] J. Bergman,et al. Studies of rutaecarpine and related quinazolinocarboline alkaloids , 1985 .
[31] F. Kurzer. 221. Cyanamides. Part I. The synthesis of substituted arylsulphonylcyanamides , 1949 .
[32] F. Kurzer. 638. Cyanamides. Part II. The influence of substituents in the synthesis of arylsulphonylarylcyanamides , 1949 .