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Methyl evernate

Deriv Methyl evernate, prisms (EtOH), mp 140 °C, from evernic acid with CHjN, in Et,0 at 20°Cin 30 s... [Pg.255]

Robertson A, Stephenson RJ (1932) Lichen acids. Part II. The constitution of evernic acid and the synthesis of methyl evernate. J Chem Soc 1388-1395... [Pg.468]

Methyl evernate OH H OMe H Me H OH C02Me Me H Pseudocyphellaria crocata Lobaria linita Peltigera aphthosa Column chromatography Spectral data and synthesis (252, 255, 234)... [Pg.160]

Methyl-evernic acid OH H OMe H Me H OMe CO2H Me H Evernia prunastri Column chromatography Spectral data ( 3c-n.m.r.) synthesis 252)... [Pg.160]

Finally aphthosin (278), an orcinol tetradepside was obtained through condensing evernic acid (279) and methyl lecanorate (280) (Scheme 36) (57). The properties of this synthetic material were identical with those of the natural product isolated by Bachelor and King 10), although a reinvestigation of the constituents of Peltigera aphthosa failed to verify the natural occurrence of this tetradepside 234). [Pg.158]

See other pages where Methyl evernate is mentioned: [Pg.34]    [Pg.107]    [Pg.115]    [Pg.270]    [Pg.124]    [Pg.9]    [Pg.84]    [Pg.245]    [Pg.34]    [Pg.107]    [Pg.115]    [Pg.270]    [Pg.124]    [Pg.9]    [Pg.84]    [Pg.245]    [Pg.228]    [Pg.229]   
See also in sourсe #XX -- [ Pg.270 ]

See also in sourсe #XX -- [ Pg.124 , Pg.160 ]

See also in sourсe #XX -- [ Pg.9 , Pg.84 ]



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