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Ergosteryl acetate tricarbonyliron

Similar reactions have been reported with various polyenes, but failed with ergosteryl acetate tricarbonyliron and the cyclooctatetraene complex (see, however, results with the use of Simmons-Smith reagent). ... [Pg.1854]

Ergosteryl acetate tricarbonyliron can be obtained in y-lTTfo yield by use of this reagent. Use of dodecacarbonyUron gives the complex in low yield. The tricarbonyliron complex is useful for protection of the diene system during reactions of the isolated double bond. ... [Pg.39]

A -Ergostadiene-Sll-ol, 502 A -5a-Ergostene-3 -ol, 502 Ergosterol, 502 Ergosteryl acetate, 100, 595 Ergosteryl acetate tricarbonyliron, 39 Erythionolide B, 215 Eschenmoser cleavage, 232-233 Eschenmoser s reagent, 106 Esterification, 106, 138, 246, 269, 274,... [Pg.374]

See also in sourсe #XX -- [ Pg.39 ]



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Ergosteryl acetate

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