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- W2045658502 abstract "[1-2H]Oct-2-ynal is converted by fermenting bakers' yeast into (1S)-[1-2H]oct-2-yn-1-ol with an enantiomeric purity of >96% as measured by Mosher's MTPA method. The alcohol, as its tosyl ester, was then converted by copper-catalysed coupling with the di-Grignard of dec-9-ynoic acid and catalytic semi-hydrogenation, into (11R)-[11-2H]linoleic acid having less than 2%E-material and >95 atom %D. Provision for (11S)-[11-2H]linoleic acid was made by configurational inversion of (1R)-[1-2H]oct-2-yn-1-ol using Mitsunobu chemistry." @default.
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- W2045658502 date "1992-01-01" @default.
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- W2045658502 title "Synthesis of linoleic acid with chiral isotopic labelling at a flanking and a medial allylic methylene: the (8R,9Z,12Z)-[8-2H] and (11R,9Z,12Z)-[11-2H]-stereoisomers, and (Z)-[2,2-2H2]non-3-enal" @default.
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- W2045658502 doi "https://doi.org/10.1039/p19920001929" @default.
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