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Meystre

Additional applications are exemplified by the well-known Meystre-Miescher degradation of the bile acid side chain and, more recently, in the preparation of a-pyrones from a,iS-unsaturated lactones. ... [Pg.333]

The mp of this substance depends on the solvent used for recrystallization. A mp of 171-174 was reported for a sample recrystallized from ether-petroleum ether [K. Heusler, J. Kalvoda, Ch. Meystre, P. Wieland, G. Anner, A. Wettstein, G. Cainelli, D. Arigoni and O. Jeger, Helv. Chim. Acta, 44, 502 (1961)]. [Pg.245]

The preparation of the title lactone has been described by a multistep synthesis from holarrhimine. The method described in detail above is essentially an application of the hypoiodite reaction published by Ch. Meystre and co-workers. These authors also describe the isolgition of the intermediate hemiacetal in pure form. Saturated lactones epimeric at C-20 have also been obtained by chromic acid oxidation of 18,20-dihydroxy compounds which were in turn prepared by treatment of 20-hydroxypregnanes with lead tetraacetate, acetolysis of the resulting 18,20 3-oxides, and hydrolysis. Saturated lactones of the... [Pg.95]

K. Heusler, J. Kalvoda, Ch. Meystre, P. Wieland, G. Anner, A. Wettstein,... [Pg.96]


See other pages where Meystre is mentioned: [Pg.106]    [Pg.141]    [Pg.259]    [Pg.260]    [Pg.261]    [Pg.261]    [Pg.368]    [Pg.421]    [Pg.121]    [Pg.229]    [Pg.230]    [Pg.233]    [Pg.233]    [Pg.284]    [Pg.284]    [Pg.285]    [Pg.285]    [Pg.285]    [Pg.285]    [Pg.286]    [Pg.968]    [Pg.968]    [Pg.800]    [Pg.332]    [Pg.843]    [Pg.1268]    [Pg.1833]    [Pg.257]    [Pg.1272]    [Pg.991]    [Pg.202]    [Pg.30]    [Pg.409]    [Pg.96]    [Pg.96]    [Pg.245]    [Pg.263]    [Pg.708]    [Pg.364]    [Pg.388]    [Pg.234]    [Pg.917]    [Pg.1376]    [Pg.297]    [Pg.301]    [Pg.301]   
See also in sourсe #XX -- [ Pg.41 ]




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Meystre-Miescher modification

Meystre-Miescher-Wettstein degradation

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