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- W2097191036 abstract "The syntheses of 9-, 13-, and 9,13-desmethyl-vitamin A are described from the corresponding desmethyl homologues of vitamin A acid methyl esters. The latter were prepared by condensation of trans-β-ionylidene acetaldehyde and trans-5-(2′,6′,6′-trimethylcyclohexene-1′-yl-1′)-pentadiene 2,4-al-1 respectively, with the phosphonates of the appropriate crotonic acid esters. Biological investigations on growth promoting properties have shown that all-trans-13- and all-trans-9,13-desmethyl vitamin A acetate are completely inactive, while all-trans-9-desmethyl vitamin A acetate exhibits an activity of about 4%, when compared with all-trans-vitamin A acetate." @default.
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- W2097191036 date "1966-01-01" @default.
- W2097191036 modified "2023-10-09" @default.
- W2097191036 title "Vitamin A analogues—V" @default.
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- W2097191036 doi "https://doi.org/10.1016/0040-4020(66)80130-8" @default.
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