Synthesis of ethyl 5-cyano-6-hydroxy-2-methyl-4-(1-naphthyl)-nicotinate

[1]  Long-min Wu,et al.  N-Nitroso-2-aryl-1,3-oxazolidines catalyzed aromatization of Hantzsch 1,4-dihydropyridines , 2008 .

[2]  M. Hundal,et al.  An efficient, catalyst- and solvent-free, four-component, and one-pot synthesis of polyhydroquinolines on grinding , 2008 .

[3]  S. Fukuzawa,et al.  Catalytic synthesis of 1,4-dihydropyridine derivatives using scandium(III) triflate , 2008 .

[4]  Zhong-Quan Liu,et al.  Aromatization of Hantzsch 1,4-dihydropyridines and 1,3,5-trisubstituted pyrazolines with HIO3 and I2O5 in water , 2006 .

[5]  H. Tian,et al.  Facile Yb(OTf)3 promoted one-pot synthesis of polyhydroquinoline derivatives through Hantzsch reaction , 2005 .

[6]  A. Kirschning,et al.  2-Pyridinealdoxime, a new ligand for a Pd-precatalyst: Application in solid-phase-assisted Suzuki–Miyaura reaction , 2005, Molecular Diversity.

[7]  G. Bringmann,et al.  The total synthesis of streptonigrin and related antitumor antibiotic natural products , 2004 .

[8]  D. Zaller,et al.  p38MAP kinase inhibitors. Part 1: design and development of a new class of potent and highly selective inhibitors based on 3,4-dihydropyrido[3,2-d]pyrimidone scaffold. , 2003, Bioorganic & medicinal chemistry letters.

[9]  C. Nájera,et al.  A convenient oxime-carbapalladacycle-catalyzed Suzuki cross-coupling of aryl chlorides in water. , 2002, Angewandte Chemie.

[10]  Y. Fujikawa,et al.  Synthesis and biological evaluations of condensed pyridine and condensed pyrimidine-based HMG-CoA reductase inhibitors. , 2001, Bioorganic & medicinal chemistry letters.

[11]  O. Mongin,et al.  Total Synthesis of (.+-.)-Atpenin B. An Original "Clockwise" Functionalization of 2-Chloropyridine , 1994 .

[12]  E. Mash,et al.  A new synthetic approach to the C-D ring portion of streptonigrin analogues , 1990 .

[13]  S. Hibino,et al.  Total synthesis of the antitumor antibiotic streptonigrin , 1982 .

[14]  T. Liao,et al.  Synthetic studies of the antitumor antibiotic streptonigrin. 3. Synthesis of the C-D ring of streptonigrin by an unsymmetrical Ullmann reaction , 1979 .