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4.6- Dihydroxy-2-methoxy-3-methylacetophenone

Dihydroxy-2-methoxy-3-methylacetophenone (4,6-Dihydroxy-2-methoxy-3-methylacetophenon)... [Pg.155]

Bolognese A, Chioccara F, Scherillo G (1974) Isolation and characterization of atranorin and 4,6-dihydroxy-2-methoxy-3-methylacetophenone from Stereocaulon vesuvianum. Phytochemistry 13 1989-1990... [Pg.449]

Hylands PJ, Ingolfsdottir K (1985) The isolation of methyl P-orsellinate from Stereocaulon alpinum and comments on the isolation of 4,6-dihydroxy-2-methoxy-3-methylacetophenone from Stereocaulon species. Phytochemistry 24 127-129... [Pg.462]

Bolognese, A., F. Chioccara, and G. Scherillo Isolation and Characterisation of Atranorin and 4,6-Dihydroxy-2-methoxy-3-methylacetophenone from Stereocaulon vesuvianum. Phytochem. 13, 1989 (1974). [Pg.220]

Preparation by reaction of methyl iodide with 4,6-dihydroxy-2-methoxy-3-methylacetophenone in the presence of potassium carbonate in refluxing acetone (93%) [3043]. [Pg.883]

Obtained by partial methylation of 2,5-dihydroxy-4-methoxy-6-methylacetophenone with dimethyl sulfate in acetone, in the presence of potassium carbonate (20%) [3050]. [Pg.884]

Also obtained by heating 2,4-dihydroxy-6-methoxy-3-methylacetophenone 4-0-a-L-arabinofuranosyl-(l—>6)-P-D-glucopyranoside with 10% HCl under reflux for 5 h [6321]. [Pg.1729]

See other pages where 4.6- Dihydroxy-2-methoxy-3-methylacetophenone is mentioned: [Pg.30]    [Pg.2890]    [Pg.2890]    [Pg.30]    [Pg.882]    [Pg.882]    [Pg.2890]   
See also in sourсe #XX -- [ Pg.155 ]



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