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16/?-Acetoxyhopan

Deriv 6a-Acetoxy-7-oxo-hopan-22-ol, mp 229-230 °C, by oxidation of 6a-acetoxyhopan-7a,22-diol with Jones reagent StL Pseudocyphellaria crocata (L.) Vain. [Pg.365]

Deriv 6-Oxo-7a-acetoxyhopan-22-ol, mp 256-257 °C, from 7a-acetoxyhopan-6a,22-diol with Jone s reagent... [Pg.365]

Deriv 15a-Acetoxyhopan-22-ol, mp 200-201 °C (n-hexane), from hopan-15a,22-diol with AcjO-pyridine... [Pg.376]

Deriv 16p-Acetoxyhopan-22-ol,mp 228°C, [a]o + 52 (CHCI3), from hopan-16p,22-diol with ACjO-pyridine... [Pg.377]

Huneck S, Preiss A, Schmidt J, Morales Mendez A (1983) 3P-Acetoxyhopan-lp,22-diol, a triterpene from the lichen Pseudoparmelia texana. Phytochemistry 22 2027-2030... [Pg.462]

See other pages where 16/?-Acetoxyhopan is mentioned: [Pg.44]    [Pg.44]    [Pg.44]    [Pg.44]    [Pg.44]    [Pg.44]    [Pg.45]    [Pg.45]    [Pg.45]    [Pg.45]    [Pg.50]    [Pg.118]    [Pg.118]    [Pg.118]    [Pg.118]    [Pg.119]    [Pg.119]    [Pg.119]    [Pg.119]    [Pg.120]    [Pg.121]    [Pg.364]    [Pg.365]    [Pg.365]    [Pg.365]    [Pg.365]    [Pg.366]    [Pg.366]    [Pg.366]    [Pg.367]    [Pg.367]    [Pg.367]    [Pg.367]    [Pg.367]    [Pg.206]    [Pg.206]    [Pg.206]    [Pg.74]    [Pg.74]    [Pg.206]    [Pg.206]    [Pg.285]    [Pg.290]   
See also in sourсe #XX -- [ Pg.22 , Pg.367 ]



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6a-Acetoxyhopan

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