Author:
Liška František,Valenta Miroslav,Fikar Jiří,Jandová Martina,Pešek Miroslav,Trška Petr
Abstract
UV-light- and γ-60Co-initiated addition of acetaldehyde to allyl formate (I) and allyl acetate (II) yielded the 1:1 adducts - 4-oxopentyl formate (III) and 4-oxopentyl acetate (IV), respectively, together with the 1:2 telomers - 7-formyloxy-4-formyloxymethyl-2-heptanone (V) and 7-acetoxy-4-acetoxymethyl-2-heptanone (VI). The initial radiation yields are: G(III) = 200·8, G(IV) = 211·3, G(V) = 39·5, G(VI) = 37·9. Base-catalyzed transesterification of oxopentyl alkanoates III and IV afforded 5-hydroxy-2-pentanone (XIV), the same reaction of dialkylalkanoates VI and VII gave 5-hydroxy-4-hydroxymethyl-2-heptanone (XV).
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
2 articles.
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