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Synthesis of [13C?]-B6 Vitamers Labelled at Three Consecutive Positions Starting from [13C?]-Propionic Acid.


ABSTRACT: [13C?]-labelled vitamers (PN, PL and PM) of the B6 group were prepared starting from [13C?]-propionic acid. [13C?]-PN was synthesized in ten linear steps with an overall yield of 17%. Hereby, higher alkyl homologues of involved esters showed a positive impact on the reaction outcome of the intermediates in the chosen synthetic route. Oxidation of [13C?]-PN to [13C?]-PL was undertaken using potassium permanganate and methylamine followed by acid hydrolysis of the imine derivative. [13C?]-PM could be prepared from the oxime derivative of [13C?]-PN by hydrogenation with palladium.

SUBMITTER: Bachmann T 

PROVIDER: S-EPMC6225105 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

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Synthesis of [<sup>13</sup>C₃]-B6 Vitamers Labelled at Three Consecutive Positions Starting from [<sup>13</sup>C₃]-Propionic Acid.

Bachmann Thomas T   Rychlik Michael M  

Molecules (Basel, Switzerland) 20180823 9


[<sup>13</sup>C₃]-labelled vitamers (PN, PL and PM) of the B6 group were prepared starting from [<sup>13</sup>C₃]-propionic acid. [<sup>13</sup>C₃]-PN was synthesized in ten linear steps with an overall yield of 17%. Hereby, higher alkyl homologues of involved esters showed a positive impact on the reaction outcome of the intermediates in the chosen synthetic route. Oxidation of [<sup>13</sup>C₃]-PN to [<sup>13</sup>C₃]-PL was undertaken using potassium permanganate and methylamine followed by a  ...[more]

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