Publications by authors named "J M Quintard"

Article Synopsis
  • A highly enantioselective method has been developed to synthesize (R,S) or (S,S)-2,6-disubstituted dehydropiperidines using Sn/Li transmetalation of stannylated compounds.
  • The study also explores dihydroxylation reactions, both syn and anti, leading to the conversion of these compounds into NH or NMe iminosugar hydrochlorides, utilizing protecting groups for stereochemical control.
  • Initial tests of the resulting iminosugar C-glycosides as glycosidase inhibitors showed potential for selectively inhibiting specific enzymes, while the synthetic method offers flexibility for designing drugs with improved biological properties.
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To test the feasibility, safety, and efficacy of partial extracorporeal CO2 removal (PECCO2R) using a standard continuous renal replacement (CRRT) device with a pediatric oxygenation membrane introduced into the circuit in a serial manner. In this retrospective single-center study, we have studied mechanically ventilated patients with persistent significant respiratory acidosis and acute renal failure requiring ongoing CRRT. Sixteen patients were treated with our PECCO2R device.

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An original access to iminosugars from a cis/trans mixture of stannylated oxazolidinones 5 is reported. The dehydropiperidines 7-trans and 7-cis were obtained stereoselectively with an RS and SS configuration depending on the order of the Sn-Li transmetalation (followed by electrophilic trapping) and of the ring closing metathesis reactions due to the stereoselective epimerization of the α-aminoanion intermediate. The dehydropiperidines 7-trans and 7-cis were subsequently used for the synthesis of enantiopure homonojirimycin analogs.

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The electrochemical reduction of sensitive sulfonamides is described. The addition of a benzoyl group on the nitrogen atom facilitates the reductive cleavage of sulfonamides preventing β-fragmentation and epimerization. This strategy was successfully applied to the cyclopropylamine and to α-amino stannanes.

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