Preparation of high specific activity all trans?螃窿?retinyl??11??3H acetate

…, W Burger, CW Perry, AA Liebman

Index: Hale; Burger; Perry; Liebman Journal of Labelled Compounds and Radiopharmaceuticals, 1977 , vol. 13, # 1 p. 123 - 135

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Citation Number: 5

Abstract

Abstract Lithium borotritide reduction of α-ionylidene-acetaldehyde (5) followed by manganese dioxide oxidation provided the tritiated aldehyde (9) which retainad over 95% of the label. On treatment with the ylide derived from ethyl 4-chloro-3-methylcrotonate, ethyl α- retinoate-11-3 H (14) was obtained which, after purification, was hydrolyzed to α-retinoic-11- 3 H acid (15). Conversion to the methyl ester (16) followed by lithium aluminum hydride ...