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- W2149968303 abstract "Beginning with (R)-pulegone, a CD 3 group attached to the stereogenic center containing CH 3 has been created by conversion to citronellal-1-d, exchange of the acidic hydrogens at C-2 by deuterium, and decarbonylation with Wilkinson's catalyst. Oxidation to isovaleric acid-d 3 and conversion to leucine by standard procedures gave the (2S,4S) and (2R,4S) diastereomers (10 and 12) of [5,5,5- 2 H 3 ]leucine." @default.
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- W2149968303 date "1994-01-01" @default.
- W2149968303 modified "2023-09-27" @default.
- W2149968303 title "Synthesis of (2<i>S</i>,4<i>S</i>)- and (2<i>S</i>,4<i>R</i>)-[5,5,5-<sup>2</sup>H<sub>3</sub>] leucine from (<i>R</i>)-pulegone" @default.
- W2149968303 doi "https://doi.org/10.1139/v94-017" @default.
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