5,6,7,8-Tetra-hydroquinolines. 5. Antiulcer and antisecretory activity of 5,6,7,8-tetrahydroquinolinethio-ureas and related heterocycles
Beattie DE, Crossley R, Curran AC, Hill DG, Lawrence AE (1977) 5,6,7,8-Tetra-hydroquinolines. 5. Antiulcer and antisecretory activity of 5,6,7,8-tetrahydroquinolinethio-ureas and related heterocycles. J Med Chem 20:718-721
Synthesis of some 3-phenyl-4-methyl-6-(6-arylpyridin-2-yl)-and 3-phenyl-4-methyl-6-(4,6-diarylpyridin-2-yl) coumarins
Brahmbhatt DI, Patel CN, Pandya VP, Patel MA (2004) Synthesis of some 3-phenyl-4-methyl-6-(6-arylpyridin-2-yl)-and 3-phenyl-4-methyl-6-(4,6-diarylpyridin-2-yl) coumarins. Indian J Chem 43B:2228-2230
Synthesis of some 3-phenyl-4-methyl-6-(6-styryl-4-arylpyridin-2-yl)-, 6-(4-styryl-6-arylpyridin-2-yl)-and 6-(4-aryl-8-aryledine-5,6,7,8-tetrahydroquinolin-2-yl)coumarins
Brahmbhatt DI, Patel CN, Pandya VP, Patel MA (2005) Synthesis of some 3-phenyl-4-methyl-6-(6-styryl-4-arylpyridin-2-yl)-, 6-(4-styryl-6-arylpyridin-2-yl)-and 6-(4-aryl-8-aryledine-5,6,7,8-tetrahydroquinolin-2-yl)coumarins. Indian J Chem 44B:1863-1867
Crossley R, Opalko A, Shepherd RG (1990) Certain cyclopenta[ b]pyridines and 5,6,7,8-tetra-hydroquinolines having anti-inflammatory activity. US patent 5112832
Synthesis and dopaminergic activity of pyridine analogs of 5-hydroxy-2-(Di-n-propylamino)tetralin
Glase SA, Corbin AE, Pugaley TA, Heffner TG, Wise LD (1995) Synthesis and dopaminergic activity of pyridine analogs of 5-hydroxy-2-(di-n-propylamino)tetralin. JMedChem38:3132-3137
Reactions with heterocycles containing a 2-acyl-2-propenone structure, III: Pyrido[3,2-c]coumarins from 3-substituted 1-benzopyrans and enamines
Heber D (1987) Reactions with heterocycles containing a 2-acyl-2-propenone structure, III: pyrido[3,2-c]coumarins from 3-substituted 1-benzopyrans and enamines. Arch Pharm 320:402-406
Asymmetric synthesis of a selective endothelin A receptor antagonist
Kato Y, Niiyama K, Jona H, Okada S, Akao A, Hiraga S, Tsuchiya Y, Tomimoto K, Mase T (2002) Asymmetric synthesis of a selective endothelin A receptor antagonist. Chem Pharm Bull 50:1066-1072
Synthesis of 4-chloro-3-formylcoumarins and some coumarino[3,4-d]isoxazoles and coumarino[3,4-d]pyrazoles derived from them
Moorty SR, Sundaramurthy V, Subba Rao NV (1973) Synthesis of 4-chloro-3-formylcoumarins and some coumarino[3,4-d]isoxazoles and coumarino[3,4-d]pyrazoles derived from them. Indian J Chem 11:854-856
A convenient synthetic method of a 5,7-diarylcyclopenteno-[1,2-b]pyridine-6-carboxylate: A key intermediate for potent endothelin receptor antagonists
Niiyama K, Yoshizumi T, Takahashi H, Naya A, Ohtake N, Fukami T, Mase T, Hayama T, Ishikawa K (2002) A convenient synthetic method of a 5,7-diarylcyclopenteno-[1,2-b]pyridine-6-carboxylate: a key intermediate for potent endothelin receptor antagonists. Bioorg Med Chem 10:3437-3444
Mushroom tyrosinase catalysed synthesis of coumestans, bebzofuranderivatives and related heterocyclic compounds
Pandey G, Muralikrishna C, Bhalerao UT (1989) Mushroom tyrosinase catalysed synthesis of coumestans, bebzofuranderivatives and related heterocyclic compounds. Tetrahedron 45:6867-6874
Structure-activity studies of novobiocin analogs as modulators of the cytotoxicity of etoposide (VP-16)
Rappa G, Shyam K, Lorico A, Fodstad O, Sartorelli AC (2000) Structure-activity studies of novobiocin analogs as modulators of the cytotoxicity of etoposide (VP-16). Oncol Res 12:113-119
A convenient synthesis of b-chloro-vinylaldehydes with bis-(Trichloromehtyl) carbonate
Su WK, Zhuang YG, Wu DZ, Zhong WH (2007) A convenient synthesis of b-chloro-vinylaldehydes with bis-(trichloromehtyl) carbonate. Org Prep Proc Int 39:195-199
Santiagonamine: A new aporphinoid alkaloid incorporating a phenanthridine skeleton
Valencia E, Patra A, Freyer AJ, Shamma M, Fajardo V (1984) Santiagonamine: a new aporphinoid alkaloid incorporating a phenanthridine skeleton. Tetrahedron Lett 25:3163-3166