Design and evaluation of dihydroisoquinolines as potent and orally bioavailable human cytomegalovirus inhibitors.
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L. Chan | N. Turcotte | J. Bédard | H. Jin | T. Stefanac | S. May | Y. Chen | Z. Hu | Z. Hu
[1] L. Chan,et al. Antiviral Properties of a Series of 1,6-Naphthyridine and 7,8-Dihydroisoquinoline Derivatives Exhibiting Potent Activity against Human Cytomegalovirus , 2000, Antimicrobial Agents and Chemotherapy.
[2] C. Bruggeman,et al. Cytomegalovirus and atherogenesis. , 1999, Antiviral research.
[3] L. Chan,et al. Discovery of 1,6-naphthyridines as a novel class of potent and selective human cytomegalovirus inhibitors. , 1999, Journal of medicinal chemistry.
[4] B. Gazzard,et al. Summary of the II International Symposium on Cytomegalovirus. , 1998, Antiviral research.
[5] J. Frost,et al. A Convenient Synthesis 7,8-Dihydroisoquinolin-5(6H)-One , 1996 .
[6] W. Stadlbauer,et al. Synthesis of aminopyridazines from azidopyridazines and tetrazolo[1,5-b]pyridazines , 1989 .
[7] W. Dmowski,et al. Polyhaloaromatics. Part II. Synthesis of octafluoro-1,3-dihydro-isobenzofuran and its conversion to tetrafluoroterephthalic acid , 1988 .
[8] A. Echavarren,et al. Palladium-catalyzed coupling of aryl triflates with organostannanes , 1987 .
[9] L. Mander,et al. Regioselective synthesis of β-ketoesters from lithium enolates and methyl cyanoformate , 1984 .
[10] Curtis D. Klaassen,et al. Casarett and Doull's Toxicology. The Basic Science of Poisons , 1981 .
[11] Yoshiro Kobayashi,et al. Studies on the Reactions of Heterocyclic Compounds. I. Syntheses and Some Reactions of 1, 6-Naphthyridine N-Oxides , 1969 .