BOM-tert-butylmethylphosphinite borane is an efficient electrophilic P-stereogenic transfer reagent for the synthesis of bulky tertiary phosphines. The novel methodology relies on a one-pot deprotection/substitution trivalent phosphinite that takes place with very high stereospecificity. potential this strategy demonstrated wide scope phosphines in excellent enantiomeric excess. was applied to ...

Different numerical and analytical models are presently available that provide the tools to predict pollutant and water transfer processes between the soil surface and the groundwater level. Among the existing models, the Hydrus-1D model has been used for years in the prediction of water and pollutants transfer in the unsaturated zone. The main purpose of this paper was to model the movement of...

Extraction-As the oxidation is essentially non-specific, the plasma extract must be as free of non-lipide reducing substances as possible. All solvents should be tested occasionally for reducing residues remaining after evaporation, and redistilled if necessary. Ether should be maintained peroxide-free. The determinations reported here followed a conventional alcohol-ether extraction and subseq...

Transition metal-free radical α-perfluoroalkylation with concomitant β-alkynylation of unactivated alkenes is presented. These cascades proceed via electron-catalysis and comprise a radical 1,4- or 1,5-alkynyl migration from tertiary propargylic alcoholates to secondary or tertiary C-radicals as the key step. Alkynyl migration leads to a ketyl radical anion that sustains the chain as a single e...

N,N'-Dibenzyl diketiminate copper isopropanolate, (nacnac(Bn)CuOiPr)(2), polymerizes rac- and S,S-lactide in the presence or absence of isopropanol as a chain-transfer reagent with very high activity (k(2) = 32 M(-1) s(-1)), narrow polydispersities and without evidence of side reactions such as transesterification, epimerization or catalyst decomposition.

Chiral phase‐transfer catalyst brings insoluble ionic halogenating reagents into the solution and mediates enantioselective halogenations by forming highly ordered asymmetric environments through ion pairing and/or hydrogen‐bonding interactions with substrate reagent. Such approaches have been enormously successful in both nucleophilic electrophilic halogenations. In this review, remarkable exa...