Search results for "cycles"

showing 10 items of 306 documents

Cyclicity of Triassic to Lower Jurassic continental red beds of the Argana Valley, Morocco: implications for palaeoclimate and basin evolution

2000

Abstract Cyclical playa deposits form a prominent part of the continental clastic succession of the Argana Valley, Western High Atlas of Morocco. The red beds formed in Triassic to Lower Jurassic times during rifting of the North American and African plates. Detailed stratigraphic work revealed asymmetrical, metre-scale cycles in mudstone-dominated successions that constitute the intermediate and upper portion of the basin fill. Sedimentary cycles commonly comprise ephemeral lake shales at the base, playa mudflat mudstones in the intermediate part, and both fluvial and aeolian sandstones at the top. Cycles of the Aglegal Member (T4) are mainly characterized by analcime-rich playa mudflat de…

Red bedsMilankovitch cyclesEphemeral keyPaleontologyFluvialCyclostratigraphyOceanographyPaleontologyClastic rockFaciesSedimentary rockEcology Evolution Behavior and SystematicsGeologyEarth-Surface ProcessesPalaeogeography, Palaeoclimatology, Palaeoecology
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Non-Classical Transformation of Benzendiazonium Hydrogen Sulfates. Access to 1,3-Dimethylisochromeno[4,3-c]pyrazol-5(1H)-one, a Potential Benzodiazep…

2013

The compound 2-((1,3-dimethyl-1H-pyrazol-5-yl)(methyl)carbamoyl)benzene-diazonium hydrogen sulfate (10) was reacted with copper sulfate and sodium chloride, in the presence of ascorbic acid as reducing agent, to afford a mixture of the chlorinated epimers 4′-chloro-2,2′,5′-trimethyl-2′,4′-dihydrospiro[isoindoline-1,3′-pyrazol]-3-one (18) and (19), the epimers 4′-hydroxy-2,2′,5′-trimethyl-2′,4′-dihydrospiro[isoindoline-1,3′-pyrazol]-3-one (20) and (21), and N-(1,3-dimethyl-1H-pyrazol-5-yl)benzamide (22). Under the foregoing conditions, diazonium salt 10 affords neither the 2-chloro-N-(1,3-dimethyl-1H-pyrazol-5-yl)-N-methylbenzamide (23) nor the tricyclic derivative 24, the classical products…

Reducing agentGABA AgentsSodiumPharmaceutical Sciencechemistry.chemical_elementSalt (chemistry)Sulfuric Acid EstersLigandsMedicinal chemistryArticleSandmeyer reactionAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryisochromeno[43-c]pyrazol-5(1H)-oneDrug DiscoverySandmeyer reactionOrganic chemistryPhysical and Theoretical ChemistryBenzamide15-hydrogen atom transferchemistry.chemical_classificationheterocyclesChemistryOrganic ChemistrySettore CHIM/06 - Chimica OrganicaDiazonium CompoundsAscorbic acidPschorr reactionReceptors GABA-ASettore CHIM/08 - Chimica FarmaceuticaIsocoumarinsChemistry (miscellaneous)Molecular MedicinePyrazolesEpimerCrystallizationisochromeno[43-<i>c</i>]pyrazol-5(1<i>H</i>)-oneDerivative (chemistry)heterocycles; Pschorr reaction; Sandmeyer reaction; 15-hydrogen atom transfer; isochromeno[43-c]pyrazol-5(1H)-oneheterocycleMolecules
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Exergy recovery during LNG regasification: Electric energy production – Part one

2009

Abstract In liquefied natural gas (LNG) regasification facilities, for exergy recovery during regasification, an option could be the production of electric energy recovering the energy available as cold. In a previous paper, the authors propose an innovative process which uses a cryogenic stream of LNG during regasification as a cold source in an improved combined heat and power (CHP) plant. Considering the LNG regasification projects in progress all over the World, an appropriate design option could be based on a modular unit having a mean regasification capacity of 2 × 109 standard cubic meters/year. This paper deals with the results of feasibility studies, developed by the authors at DRE…

RegasificationExergyEngineeringRegasificationPower stationExergy recoverybusiness.industryImproved CHP cyclesImproved CHP cycleEnergy Engineering and Power TechnologyMechanical engineeringContext (language use)Liquefied natural gas Regasification Exergy recoveryHeliumIndustrial and Manufacturing EngineeringElectric energyElectric energy productionLiquefied natural gasSettore ING-IND/10 - Fisica Tecnica IndustrialeProduction (economics)MetrebusinessProcess engineeringLiquefied natural gasApplied Thermal Engineering
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Optimization of a new lead promoting the readthrough of the nonsense mutations for CFTR rescue in human CF cells

2017

Optimization of a new lead promoting the readthrough of the nonsense mutations for CFTR rescue in human CF cells Laura Lentini, Raffaella Melfi, Sara Baldassano, Marco Tutone, Aldo Di Leonardo, Andrea Pace, Ivana Pibiri Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo Background and rationale Cystic Fibrosis patients with nonsense mutations in the CFTR gene have a more severe form of the disease. Nonsense mutations represent about 10% of the mutations that affect the CFTR gene and they are frequently associated to the classical F508 mutation (1). A potential treatment for this genetic alteration is to promote the translationa…

Settore BIO/18 - Genetica-Fluorinated heterocycles -Nonsense Mutations -Premature stop codon -ReadthroughSettore BIO/11 - Biologia MolecolareSettore CHIM/06 - Chimica OrganicaSettore BIO/09 - FisiologiaSettore CHIM/08 - Chimica Farmaceutica
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Sunlight-induced reactions of some heterocyclic bases with ethers in the presence of TiO2. A green route for the synthesis of heterocyclic aldehydes

2005

Settore CHIM/03 - Chimica Generale e InorganicaheterocyclesethersaldehydesTiO2sunlightPhotocatalysisPhotocatalysis; TiO2; sunlight; ethers; heterocycles; aldehydes;
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Novel ANRORC rearrangements of 1,2,4-oxadiazoles

2010

Settore CHIM/06 - Chimica OrganicaAnrorc rearrangement oxadiazole triazole fused heterocycles
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Bioactive Azoles with Three Heteroatoms

2010

This issue is dedicated to scientists belonging to either or both the fields of heterocyclic and medicinal chemistry. Nowadays, pharmaceutical industries are more and more dedicating their research towards different use or applications of the same molecule rather than towards the development of new drugs. In the latter decades, in fact, the time which is necessary since a given molecule is synthesized to when it is approved as a drug has significantly increased. Therefore, the development of time-saving methodologies such as combinatorial chemistry and computationally driven drug design has attracted the interest of several organic and medicinal chemists. Many of the molecules tested in-vit…

Settore CHIM/06 - Chimica OrganicaBioactive Compounds Azoles HeterocyclesSettore CHIM/08 - Chimica Farmaceutica
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New examples of specific base catalysis in mononuclear rearrangements of heterocycles found via a designed modification of the side chain structure

2009

To select suitable candidates for the occurrence of specific-base-catalysis in MRH of (Z)-hydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazole we have designed a modification of the side-chain structure by linking a strong electron-withdrawing system to the hydrazono group. Thus we have synthesized the (Z)-semicarbazone (3d), the (Z)-phenylsemicarbazone (3e), and the (Z)-acetylhydrazone (3f) of the above oxadiazole and examined their kinetic behavior in dioxane/water in a large range of proton concentrations (pS + 4.0 14.5). In all the pS+ range examined only a base-catalyzed process has been evidenced (no uncatalysed path occurs). The behavior at the largest pS+ values (the reactivity tends t…

Settore CHIM/06 - Chimica OrganicaMononuclear rearrangement of heterocycles base catalysis kinetic measurements
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Functionalised Imidazolium Dicationic Ionic Liquids used as reaction media for base catalyzed organic reactions

Settore CHIM/06 - Chimica Organicatask specific ionic liquids base catalysis mononuclear rearrangement of heterocycles.
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BIOSYNTHESIS OF HEROCYCLES. FROM ISOLATION TO GENE CLUSTER

2015

This book describes biosynthetic methods to synthesize heterocyclic compounds, offering a guide for the development of new drugs based on natural products. The authors explain the role of natural products in chemistry and their formation along with important analytical methods and techniques for working with heterocycles. • Covers methods and techniques: isotopic labelling, enzymes and mutants, and pathway identification • Provides a thorough resource of information specifically on heterocyclic natural products and their practical biosynthetic relevance • Explains the role of natural products in chemistry and their formation • Discusses gene cluster identification and the use of biogenetic …

Settore CHIM/08 - Chimica FarmaceuticaBIOSYNTHESIS HETEROCYCLES GENE CLUSTER
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