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  • NoteA kinetic study on the reductive opening of the diphenylmethylene acetal in methyl 2,3-O-diphenylmethylene-α-l-rhamnopyranoside

  • Add time:09/24/2019    Source:sciencedirect.com

    Reductive opening of the diphenylmethyl acetal in methyl 2,3-O-diphenylmethylene-α-l-rhamnopyranoside has been investigated by kinetic studies, and the results have been compared to those recently obtained by quantum chemical calculations. In contrast to the previous theoretical calculations which related only to the presumably rate limiting step of the reductive opening, the reaction system LiAlH4, AlCl3, and the title compound consists of at least four simultaneous reactions. Nevertheless, reasonable agreement can be found between the activation Gibbs free energy obtained from kinetic measurements and the theoretically calculated ones in spite of the experimental errors and the approximate nature of theoretical calculations.

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    Prev:Reaction of α,β-unsaturated Fischer carbene complexes with allyl alkoxide
    Next:Stannylene acetal-mediated regioselective open glycosylation of methyl β-d-galactopyranoside and methyl α-l-rhamnopyranoside)

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