Issue 0, 1973

Cycloadducts of ergosterol with azo-type dienophiles, and their chemical reactivities

Abstract

The 1,4-cycloadduct of ergosteryl acetate with pyridazine-3,6-dione was made and used in a synthesis of 3β-acetoxycholesta-5,7,22-triene. The Cycloadducts of ergosteryl acetate with 4,5-dihydropyridazine-3,6-dione, phthalazine-1,4-dione, and 4-phenyl-1,2,4-triazoline-3,5-dione were also prepared. Selective hydrogenation of the 22,23-double bond was not achieved in any of these Cycloadducts.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1973, 888-891

Cycloadducts of ergosterol with azo-type dienophiles, and their chemical reactivities

P. E. Georghiou and G. Just, J. Chem. Soc., Perkin Trans. 1, 1973, 888 DOI: 10.1039/P19730000888

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