Synthesis of cytotoxic maesaquinone bearing a 2,5-dihydroxy-6-methyl-1,4-benzoquinone nucleus

[1]  Y. Fukuyama,et al.  Naturally occurring 5-lipoxygenase inhibitors. VI. Structures of ardisiaquinones D, E, and F from Ardisia sieboldii. , 1995, Chemical & pharmaceutical bulletin.

[2]  Y. Fukuyama,et al.  Total synthesis of ardisiaquinone A, a potent 5-lipoxygenase inhibitor, isolated from Ardisia sieboldii, and degree of 5-lipoxygenase inhibitory activity of its derivatives. , 1994, Chemical & pharmaceutical bulletin.

[3]  I. Kubo,et al.  Structure of maesaquinone , 1994 .

[4]  Y. Fukuyama,et al.  Naturally occurring 5-lipoxygenase inhibitor. II. Structures and syntheses of ardisianones A and B, and maesanin, alkenyl-1,4-benzoquinones from the rhizome of Ardisia japonica. , 1993, Chemical & pharmaceutical bulletin.

[5]  J. Yadav,et al.  A practical preparation of functionalized alkylbenzoquinones: synthesis of maesanin and irisquinone , 1992 .

[6]  R. Sakai,et al.  Biologically active natural products , 1990 .

[7]  R. Danheiser,et al.  Total synthesis of the host defense stimulant maesanin , 1990 .

[8]  I. Kubo,et al.  Isolation, structure and synthesis of maesanin, a host defense stimulant from an african medicinal plant , 1987 .

[9]  O. Reinaud,et al.  Premiere synthese totale d'une hydroxy-methoxy-quinone: la dihydromaesanine , 1985 .

[10]  G. Feutrill,et al.  Reactions with thioethoxide ion in dimethylformamide. I. Selective demethylation of aryl methyl ethers , 1972 .

[11]  S. Natori,et al.  Hydroxybenzoquinones from Myrsinaceae Plants. III. The Structures of 2-Hydroxy-5-methoxy-3-pentadecenylbenzoquinone and Ardisiaquinones A, B and C from Ardisia spp. , 1968 .