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D-Erythropentose

The utility of l,3-dichloro-l,l,3,3-tetraisopropyldisiloxane was extended to include open-chain polyhydroxy compounds. Glycerol reacted to form the eight-membered ring (eq 4) while the D-erythropentose derivative gave only the seven-membered ring (eq 5). This strategy was used as a key step in the synthesis of the steroid 19-norcanrenone. ... [Pg.230]

See other pages where D-Erythropentose is mentioned: [Pg.219]    [Pg.93]    [Pg.17]    [Pg.219]    [Pg.93]    [Pg.17]   
See also in sourсe #XX -- [ Pg.6 , Pg.360 , Pg.364 , Pg.463 ]



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C4-P bond analogs of D-erythropentose

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