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Olivier David

Publications and source records attributed to Olivier David.

20 records · Page 2Linked to original sources

Estimation of neural dynamics from MEG/EEG cortical current density maps: application to the reconstruction of large-scale cortical synchrony.

There is a growing interest in elucidating the role of specific patterns of neural dynamics--such as transient synchronization between distant cell assemblies--in brain functions. Magnetoencephalography (MEG)/electroencephalography (EEG) recordings consist in the spatial integration of the activity from large and multiple remotely located populations of neurons. Massive diffusive effects and poor signal-to-noise ratio (SNR) preclude the proper estimation of indices related to cortical dynamics from nonaveraged MEG/EEG surface recordings. Source localization from MEG/EEG surface recordings with its excellent time resolution could contribute to a better understanding of the working brain. We propose a robust and original approach to the MEG/EEG distributed inverse problem to better estimate neural dynamics of cortical sources. For this, the surrogate data method is introduced in the MEG/EEG inverse problem framework. We apply this approach on nonaveraged data with poor SNR using the minimum norm estimator and find source localization results weakly sensitive to noise. Surrogates allow the reduction of the source space in order to reconstruct MEG/EEG data with reduced biases in both source localization and time-series dynamics. Monte Carlo simulations and results obtained from real MEG data indicate it is possible to estimate non invasively an important part of cortical source locations and dynamic and, therefore, to reveal brain functional networks.

Action Potentials↗

Enamino Ester Reduction: A Short Enantioselective Route to Pyrrolizidine and Indolizidine Alkaloids. Synthesis of (+)-Laburnine, (+)-Tashiromine, and (-)-Isoretronecanol.

Various chiral pyrrolidine tetrasubstituted beta-enamino esters were reduced catalytically or chemically with good to moderate diastereoselectivity owing to a chiral induction originated from (S)-alpha-methylbenzylamine. With endocyclic double bond compounds, the best result was obtained using PtO(2) as hydrogenation catalyst and led to a major syn addition product (e.d. 90%). In the case of exocyclic double bond compounds, hydrogenation over Pd/C gave rise to the higher diastereoselectivity and mainly afforded the unexpected anti addition product (e.d. 84%). The scope of these reductions has been extended to the synthesis of three pyrrolizidine or indolizidine alkaloids: (+)-tashiromine, (+)-laburnine, and (-)-isoretronecanol. Syntheses of these natural products, starting from chiral beta-enamino diesters, were achieved in a short and convenient manner, leading to enantiopure compounds in good overall yields.

Journal Article↗