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Chiral [2H]-labelled methylene groups in trienoic and dienoic fatty acids a facile approach via asymmetric epoxidation of [2H] allyl alcohols

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Neumann, C., & Boland, W. (1990). Chiral [2H]-labelled methylene groups in trienoic and dienoic fatty acids a facile approach via asymmetric epoxidation of [2H] allyl alcohols. Helvetica Chimica Acta, 73(3), 754-761. doi:10.1002/hlca.19900730324.


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]