In this paper we show that the neutrino observables, including an information about the transverse neutrino spin polarization, can be sensitive to the effects coming from the interference terms between the standard vector V, axial A couplings of L-handed neutrinos and exotic scalar S coupling of R-handed ones in the differential cross section. Our analysis is based on the electron neutrino-elec...

BCl3 -induced borylative cyclization of aryl-alkynes possessing ortho-EMe (E=S, O) groups represents a simple, metal-free method for the formation of C3-borylated benzothiophenes and benzofurans. The dichloro(heteroaryl)borane primary products can be protected to form synthetically ubiquitous pinacol boronate esters or used in situ in Suzuki-Miyaura cross couplings to generate 2,3-disubstituted...

We analyze near-threshold cross section data for the reaction pp→ppφ published by the DISTO collaboration and recent, still preliminary results presented by the ANKE Collaboration. We formulate a procedure to evaluate the OZI ratio at low energies by taking into account corrections from the kinematics and the final-state interaction. Combining the new data with the few measurements available at...

[reaction: see text] The 1-fluoro-1-haloalkenes undergo Pd-catalyzed Negishi cross-couplings with primary alkylzinc bromides to give multisubstituted fluoroalkenes. The alkylation was trans-selective giving pure Z-fluoroalkenes in most cases. The highest yields were obtained with Pd2(dba)3 and PdCl2(dppb) catalysts but the best stereochemical outcome was obtained with less reactive Pd(PPh3)4. T...

We calculate the one-quark-loop amplitude for the low energy γγ → ππ collision in the context of the Nambu and Jona-Lasinio model with scalar and pseudoscalar four quark couplings to all orders in the external momenta. We show that the NJL predictions for the γγ → π + π − reaction are not far from the Born amplitude, which is close to the data, and is compatible with the chiral perturbation the...

The title azaazulene 3 was synthesized either by reaction of tropone with N-{(2-pyridyl)acetyl}pyridinium iodide in the presence of ammonium acetate or by palladium-catalyzed cross-couplings between 2-halo-1-azaazulene and 2-substituted pyridine. The compound shows relatively stronger basicity compared with 2,2’-bipyridyl. While 3 showed no emission from the S1 state but from the S2 state like ...