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Development of a continuous process for enol esters of fatty acids

✍ Scribed by J. C. Craig; M. F. Kozempel; H. I. Sinnamon; M. J. Calhoun; W. K. Heiland

Book ID
112822466
Publisher
Springer-Verlag
Year
1977
Tongue
English
Weight
690 KB
Volume
54
Category
Article
ISSN
0003-021X

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## Abstract The enolates of fatty acid methyl esters 1a–g are dimerized in good yields (56 to 73%) by means of oxidative coupling with copper(II) bromide to dialkylated succinic esters 2a–g. The configuration of __meso__‐2a was established by independent synthesis. On treatment with ozone the unsat