Recent tests for the statistical parton distributions

We compare some recent experimental results obtained at DESY, SLAC and Jefferson Lab., with the predictions of the statistical model, we have previously proposed. The result of this comparison is very satisfactory.Comment: 12 pages, 6 eps figures, version to appear in Mod. Phys. Lett.

Sea-quark flavor asymmetry in the nucleon from a relativistic analysis of the Drell-Yan scattering off nuclei

It is shown that accounting for the relativistic structure of the deuteron allows to explain the ratio of the Drell-Yan pair production cross-section at the low Bjorken $x$ off the deuteron and the proton. Thus, the sea quark distributions in the nucleon should be studied with accounting for the effects of the relativistic structure of the deuteron. The suggested approach reduces theoretical uncertainty in extracting the ratio $\bar u/\bar d$ from the data and it is important for the clarification of the nature of the sea quark asymmetry in the nucleon.Comment: 4 pages, 1 figures, Chiral Symmetry in Hadron and Nuclear Physics November 13-16, 2007, Osak

Catalytic intramolecular hydroamination of aminoallenes using titanium and tantalum complexes of sterically encumbered chiral sulfonamides

Catalysis using earth abundant metals is an important goal due to the relative scarcity and expense of precious metal catalysts. It would be even more beneficial to use earth abundant catalysts for the synthesis of common pharmaceutical structural motifs such as pyrrolidine and pyridine. Thus, developing titanium catalysts for asymmetric ring closing hydroamination is a valuable goal. In this work, four sterically encumbered chiral sulfonamides derived from naturally occurring amino acids were prepared. These compounds undergo protonolysis reactions with Ti(NMe₂)₄ or Ta(NMe₂)₅ to give monomeric complexes as determined by both DOSY NMR and X-ray crystallography. The resulting complexes are active for the ring closing hydroamination hepta-4,5-dienylamine to give a mixture of tetrahydropyridine and pyrrolidine products. However, the titanium complexes convert 6-methylhepta-4,5-dienylamine exclusively to 2-(2-methylpropenyl)pyrrolidine in higher enantioselectivity than those previously reported, with enantiomeric excesses ranging from 18–24%. The corresponding tantalum complexes were more selective with enantiomeric excesses ranging from 33–39%

Parton energy loss limits and shadowing in Drell-Yan dimuon production

A precise measurement of the ratios of the Drell-Yan cross section per nucleon for an 800 GeV/c proton beam incident on Be, Fe and W targets is reported. The behavior of the Drell-Yan ratios at small target parton momentum fraction is well described by an existing fit to the shadowing observed in deep-inelastic scattering. The cross section ratios as a function of the incident parton momentum fraction set tight limits on the energy loss of quarks passing through a cold nucleus