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

Neumann, C.; Boland, W.

doi:10.1002/hlca.19900730324

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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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Citation

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: https://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]