Location of olefinic links in long-chain esters by methoxymercuration–demercuration followed by gas chromatography–mass spectrometry
Abstract
The position of double bonds in mono- and poly-enoic long-chain esters may be conveniently determined by reduction of their methoxymercuration products with sodium borohydride followed by combined gas chromatography–mass spectrometry of the resulting methoxylated esters.
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