Search results for " Synthesis"

Design Synthesis and Biological/Biophysical Evaluation of New Oligopyrrole Carboxamides, Biscarbazoles, Oxocarbazoles and Benzo[a]carbazoles: Antitum…

2006

<strong>In Silico Repurposing, Design, Synthesis and Biological Evaluation of Bisacodyl Analogues</strong>

2018

In a recent article was described in silico repositioning, design, synthesis, biological evaluation and structure-activity relationship (SAR) of an original class of anti-inflammatory agents based on a polyaromatic pharmacophore structurally related to bisacodyl (BSL) drug used in therapeutic as laxative.

Enantiomeric separation of amphetamine and related compounds by liquid chromatography using precolumn derivatization witho-phthaldialdehyde

2002

The utility of the derivatization reagento-phthaldialdehyde (OPA) in combination with the chiral thiol N-acetyl-L-cysteine (NAC) for the enantioselective analysis of primary amphetamines and structurally related substances has been investigated. The diastereomers obtained have been chromatographed on an achiral, reversed phase C18 column (125 mm×4 mm i.d., 5 μm), and detected fluorimetrically. The influence of parameters affecting the chromatographic separation as well as the derivatization reaction has been optimized, using amphetamine, norephedrine, norepinephrine and 3,4-methylenedioxyamphetamine (MDA) as model compounds. On the basis of the results obtained, possible conditions for the …

New reactions and step economy: the total synthesis of (±)-salsolene oxide based on the type II transition metal-catalyzed intramolecular [4+4] cyclo…

2006

Studies on the viability of the type II nickel-catalyzed intramolecular [4+4] cycloaddition of bis-dienes show that it is influenced by both diene substitution and geometry. Both E- and Z-isomers of 19 and 20 react, albeit at markedly different rates, to afford cycloadducts, whereas only the Z-isomer of 9 (and not the E-isomer) reacts to give 8 and 25. Chemoselective elaboration of 8 to (±)-salsolene oxide (7) was used to confirm the cycloadduct structure while establishing a step economical route to the natural product.

Diastereoselective synthesis of spongian diterpenes. Total synthesis of the furanoditerpene (−)-spongia-13(16),14-diene

1999

Abstract An effective diastereoselective synthesis of the marine-sponge metabolite (−)-spongia-13(16),14-diene 1 is achieved starting from S-(+)-carvone via a homochiral phenanthrenone as the key intermediate for the construction of the furan ring system. S-(+)-Carvone was transformed into the phenanthrenone 2a in six steps (53% overall yield), using an intramolecular Diels-Alder reaction as the key step. Conversion of the enone function in 2a into an epoxyaldehyde function followed by cyclisation and aromatisation in acid conditions completed the construction of ring D.

Influence of the pH on the ZnO nanoparticle growth in supercritical water: Experimental and simulation approaches

2014

Abstract In order to improve the knowledge on the nucleation and the growth mechanisms of metal oxides nanoparticles produced in supercritical water domain, ZnO was used as a “model” material. A continuous process of hydrothermal synthesis was employed to synthesize ZnO nanopowders ( T  = 410 °C and P  = 305 bar) from Zn(NO 3 ) 2 and KOH solutions with different values of [KOH]/[Zn(II)] ratio from 0 to 8 in order to investigate the pH effect on the growth of ZnO nanocrystallite in terms of size and morphology. The samples were characterized by X-Ray Diffraction and Transmission Electronic Microscopy. ZnO crystal was considered as a cylindrical crystallite with a diameter D and height H . Es…

Mechanically Activated SHS Reaction in the Fe-Al System: In Situ Time Resolved Diffraction Using Synchrotron Radiation

1998

The Mechanical Activation Self propagating High temperature Synthesis (M.A.S.H.S.) processing is a new way to produce nanocrystalline iron aluminide intermetallic compounds. This process is maily the combination of two steps ; in the one hand, a mechanical activation where the Fe - Al powder mixture was milled during a short time at given energy and frequency of shocks and in the other hand, a Self propagating High temperature Synthesis (S.H.S.) reaction, for which the exothermicity of the Fe + Al reaction is used. This fast propagated MASHS reaction has been in -situ investigated using the Time Resolved X - Ray Diffraction (TRXRD) using a X - ray synchrotron beam and an infrared thermograp…

Enhancement of self-sustaining reaction by mechanical activation: case of an FeSi system

1999

Mechanical high energy ball milling of an Fe2Si elemental powders mixture was used to activate a self sustaining combustion reaction or so-called self-propagating high-temperature synthesis (SHS) to form iron disilicide, a reaction for which the thermodynamic criterion is not favorable. A complete characterization of the milled powders before reaction was performed with energy dispersive X-ray spectrometry, specific surface measurements and X-ray diffraction profile analysis. Thermal and structural information describing the combustion front initiated by heating up a sample to 400°C in a Fe‐Si system is communicated. In order to isolate the phases involved in the gasless reaction, a time-re…

Time-resolved XRD experiments for a fine description of mechanisms induced during reactive sintering

2005

The control of Mechanically Activated Field Activated Pressure Assisted Synthesis hereafter called the MAFAPAS process is the main objective to be achieved for producing nanostructure materials with a controlled consolidation level. Consequently, it was essential to develop characterization tools "in situ" such as the Time Resolved X-ray Diffraction (TRXRD), with an X-ray synchrotron beam (H10, LURE Orsay) coupled to an infrared thermography to study simultaneously structural transformations and thermal evolutions. From the 2003 experiments, we took the opportunity to modify the sample-holder in order to reproduce the better synthesis conditions of the MAFAPAS process, but without the conso…

In situ synchrotron characterization of mechanically activated self-propagating high-temperature synthesis applied in Mo–Si system

1999

Abstract An original experiment was designed to monitor structural and thermal evolutions during the MASHS (Mechanically Activated Self-propagating High-temperature Synthesis) process in the Mo–Si system. Time-Resolved X-Ray Diffraction (TRXRD) coupled with an infrared imaging technique was performed to study, in situ, the formation of the α-MoSi2 phase in the combustion front. Despite a temporal resolution of 50 ms between two consecutive diffractograms, no intermediate phase was observed during the passage of the combustion front. The only reaction responsible for the self-sustentation is Mo+2Si→MoSi2 in the primary zone inside the combustion wave. The mechanical activation was found to i…