A highly effective synthesis of 2-alkynyl-7-azaindoles: Pd/C-mediated alkynylation of heteroaryl halides in water

The reaction of 4-chloro-2-iodo-7-azaindole with terminal alkynes was investigated using 10% Pd/C-PPh₃-CuI as a catalyst system in water. This study afforded a new, mild and selective process for the preparation of 2-alkynyl-4-chloro-7-azaindole in good yields via C-C bond forming reaction. The resulting chloro derivative can be functionalized further via another Pd-mediated C-C bond forming reaction with arylboronic acid.     

Anti-inflammatory chromone alkaloids and glycoside from Dysoxylum binectariferum

Herein we report isolation of a new chromone alkaloid chrotacumine K (12) from fruits and a chromone glycoside schumaniofioside A (13) from leaves of Dysoxylum binectariferum Hook f. Schumaniofioside A is reported for the first time from Meliaceae family. Other known alkaloids isolated include rohitukine (1) and chrotacumine E (6). The structure of new alkaloid 12 was elucidated on the basis of extensive 1D and 2D NMR analysis, synthesis and chemical hydrolysis. Chemically, chrotacumine K (12) is a 3′-O-acetyl rohitukine which on chemical or enzymatic hydrolysis produces rohitukine. The new alkaloid 12 is also present in seeds and stem-barks of this plant. The glycoside schumaniofioside A (13) is present only in leaves, and in abundance (～1% w/w of dried leaves). The isolated compounds and extracts were evaluated for in vitro effect on the proinflammatory cytokines (TNF-α and IL-6) in human monocytic THP-1 cells. The alkaloid 12 displayed potent inhibition (57%) of TNF-α at 0.3 µM, and was non-toxic to THP-1 cells up to 40 µM, indicating its excellent therapeutic window. Furthermore, a nitrobenzoyl ester analog 15e showed better inhibition of IL-6 than parent natural product chrotacumine K.     

Thermoluminescence studies of UV-irradiated Y2O3:Eu3+ doped phosphor

The present paper reports thermoluminescence (TL) glow curves of Eu³⁺-doped Y₂O₃ phosphor with different ultraviolet (UV) exposure times. The glow peak shows second-order kinetics of Eu³⁺-doped Y₂O₃, and corresponding kinetic parameters were evaluated using the peak shape method. Calculations of trap depth were carried out using different methods. The kinetics order, activation energy, and frequency factor were calculated. The recorded glow curve shifts towards higher intensity with longer UV exposure. The heating rate used for recording TL was 3.0 °C s^?1. Particle size and structure were verified by X-ray diffraction (XRD) pattern and morphology by scanning electron microscopy (SEM) imaging.     

Concentrated solar radiation-assisted one-pot/multicomponent synthesis of pyranopyrazole derivatives under neat condition

Research on Chemical Intermediates - Concentrated solar radiation (CSR)-assisted synthesis of pyranopyrazole derivatives under solvent and catalyst-free condition has been reported in the present...     

Chiral Lagrangian and skyrmion from quark and parity-doublet determinants

We consider the effective action of the chiral quark model to leading order in the number of colors. A set of massive ghost-like Gervais-Lee fermion doublets is introduced which effectively simulate an asymptotically free behavior for the quarks at short distances. This suppresses the vacuum instability and leaves the Wess-Zumino sector unspoiled. At small momenta, we show that the action generated in this way compares well with experiment by performing a chiral expansion up to fourth order. It is found that this action supports stable soliton solutions with baryon number one. Masses, mass-splittings and the sigma-term are estimated in theSU(2) limit.Unité de Recherche des Universités Paris 11 et Paris 6 associée au CNRS     

Review of the preparation,characterization, and luminescence properties of Pr3+-doped CaTiO3 phosphors

Research on Chemical Intermediates - In this paper we review the luminescence properties of Pr3+-doped CaTiO3 phosphors, the different methods of sample preparation, and characterization of the...