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Journal Article

Chiral Deuterium-Labelled Methylene Groups in Trienoic and Dienoic Fatty Acids a Facile Approach Via Asymmetric Epoxidation of Deuterated Allyl Alcohols

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Neumann, C., & Boland, W. (1990). Chiral Deuterium-Labelled Methylene Groups in Trienoic and Dienoic Fatty Acids a Facile Approach Via Asymmetric Epoxidation of Deuterated Allyl Alcohols. Helvetica Chimica Acta, 73(3), 754-761.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0012-A23F-9
Abstract
Chiral [2H]-labelled methylene groups flanked by two double bonds within (poly)unsaturated fatty acids are readily available from trans-2,3-epoxy[2,3-2H2]alk-4-yn-l-ols, obtained in their turn by asymmetric epoxidation of the corresponding (E)-[2,3-2H2]