Search results for " clero"

showing 10 items of 11 documents

Notulae to the Italian alien vascular flora: 2

2016

In this contribution, new data concerning the Italian distribution of alien vascular flora are presented. It includes new records, exclusions and confirmations for Italy or for Italian administrative regions for taxa in the genera Ageratum, Aster, Buddleja, Cedrus, Centranthus, Cephalotaxus, Clerodendrum, Cotoneaster, Cyperus, Honorius, Lantana, Ligustrum, Morus, Muscari, Oenothera, Opuntia, Platycladus, Plumbago, Pseudotsuga, Sedum, Sporobolus, Stachys, Ulmus and Yucca. A nomen novum, Stachys talbotii, is proposed as a replacement name for Sideritis purpurea.

0106 biological sciencesnew combinationClerodendrumUlmusLantanaLigustrumAgeratum Aster Buddleja Cedrus Centranthus Cephalotaxus Clerodendrum Cotoneaster Cyperus Honorius Lantana Ligustrum Morus Muscari Oenothera Opuntia Platycladus Plumbago Pseudotsuga Sedum Sporobolus Stachys Ulmus YuccaZoologyAlienPlant ScienceAgeratumPlatycladusBiologyCentranthus010603 evolutionary biology01 natural sciencesSedumCephalotaxusSporoboluslcsh:BotanyYuccaCyperusCedrusEcology Evolution Behavior and SystematicsAsterPlumbagoFloristic data ItalySettore BIO/02 - Botanica SistematicaHonoriusOpuntiaFloristic dataCotoneasterMuscariPseudotsugalcsh:QK1-989GeographyItalyOenotheraSettore BIO/03 - Botanica Ambientale E ApplicataItalian FloraStachysMorusBuddleja010606 plant biology & botany
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Complete 1H and 13C NMR assignments of clerodane diterpenoids of Salvia splendens.

2006

Unambiguous and complete assignments of 1H and 13C NMR chemical shifts for five clerodane diterpenes, four of them isolated from Salvia splendens (salviarin, splendidin and splenolides A and B) and one obtained by acetylation of splenolide A, are presented. The assignments are based on 2D shift-correlated [1H,1H–COSY, 1H,13C-gHSQC–1J(C,H) and 1H,13C-gHMBC-nJ(C,H) (n = 2 and 3)] and nuclear Overhauser effect (NOE) experiments. The conformation of the rings of these compounds is supported by the 3J(H,H) values and NOE results. Copyright © 2006 John Wiley & Sons, Ltd.

Carbon IsotopesMagnetic Resonance SpectroscopybiologyStereochemistryChemistryChemical shiftAcetylationGeneral ChemistryNuclear Overhauser effectCarbon-13 NMRSalviabiology.organism_classificationDiterpenes ClerodaneUnambiguous and complete assignments of 1H and 13C NMR chemical shifts for five clerodane diterpenes four of them isolated from Salvia splendens (salviarin splendidin and splenolides A and B) and one obtained by acetylation of splenolide A are presented. The assignments are based on 2D shiftcorrelated [1H1H–COSY 1H13C-gHSQC–1J(CH) and 1H13C-gHMBC-nJ(CH) (n = 2 and 3)] and nuclear Overhauser effect (NOE) experiments. The conformation of the rings of these compounds is supported by the 3J(HH) values and NOE results. Copyright  2006 John Wiley & Sons LtdClerodane DiterpenesProton NMRGeneral Materials ScienceSalviaHydrogenMagnetic resonance in chemistry : MRC
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Sulle donazioni da parte degli istituti di sostentamento del clero

2003

Chiesa donazioni clero
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Una lectura teológica del sermón de José María Cos

2015

<p>El presente trabajo hace una lectura teológica de un sermón insurgente de José María Cos y puede ser considerado un capítulo en la historia de la teología en América Latina, un área todavía poco desarrollada, y es necesario hacer nuevos estudios en este campo. El artículo se inserta en la nueva historiografía que se ha interesado por la religiosidad de los curas insurgentes y resalta la motivación cristiana del padre Cos, quien se había volcado hacia la praxis política de la independencia de México motivado en primera instancia por su fe cristiana. El artículo concluye aseverando que José María Cos forma entonces parte de una larga tradición de sacerdotes políticos en la historia d…

Cultural StudiesIglesia y clerolcsh:Latin America. Spanish AmericaHistoryPraxisSociology and Political Sciencelcsh:HN1-995Interpretation (philosophy)media_common.quotation_subjectlcsh:F1201-3799discurso retóricoHistoriographyHistory of theologylectura teológicaIndependenceReligiosityPoliticsindependencia de MéxicoSociologylcsh:Social history and conditions. Social problems. Social reformReligious studiesJosé María CosSermonHumanitiesmedia_commonSecuencia
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Hastifolins A-G, antefeedant neo-clerodane diterpenoids from Scutellaria hastifolia

2010

From the aerial parts of Scutellaria hastifolia, family Lamiaceae (Labiatae), seven neo-clerodane diterpenoids (hastifolins A-G) were isolated. The products are similar to the known scuteparvin and are characterized by being trans-cinnamoyl derivatives. Structures and stereochemistry were determined by intensive NMR investigation. Six of the products form three pairs of epimers at C-13. Hastifolins A-C showed significant antifeedant activity.

Family LamiaceaeStereochemistryScutellariaChemical structurePlant ScienceHorticultureSpodopteraBiochemistryDiterpenes Clerodanechemistry.chemical_compoundFeeding behaviorAnimalsMolecular BiologyNuclear Magnetic Resonance BiomolecularbiologyMolecular StructureGeneral MedicineFeeding BehaviorSettore CHIM/06 - Chimica Organicabiology.organism_classificationTerpenoidchemistryLarvaScutellariaLamiaceaeEpimerDiterpeneScutellaria hastifolia Lamiaceae diterpenes neo-clerodanes epimers antifeedant
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Phytochemical study of Cistus libanotis L.

2015

n continuation of our ongoing study on Mediterranean Flora, we focused the attention on Cistus genus. These plants possess interesting secondary metabolites and are used in many fields, principally in perfumery and more recently as raw material for food supplements (botanicals). n this article, we report the phytochemical analysis of Cistus libanotis L. from Tunisia. Among the diterpenes, labdane compounds resulted absent, in favour of two clerodanes, one of that never reported in Cistus sp. The main representative compounds were found to be several flavonoids with various grades of O-methylation. Other interesting components were two cinnamic esters of borneol, reported here for the first …

FloraTunisiaCistuPlant ScienceCistus libanotisBiochemistryditerpeneBorneolDiterpenes ClerodanePlant ExtractAnalytical ChemistryLabdanechemistry.chemical_compoundGenusCistusBotanycistus libanotis; clerodane; diterpene; phenolsphenolbiologyMolecular StructurePlant ExtractsOrganic ChemistryCistusbiology.organism_classificationPlant LeaveschemistryPhytochemicalclerodaneCistus libanotiDiterpenePlant Leave
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Extremely potent antifeedant neo-clerodane derivatives of scutecyprol A

2004

Two known neo-clerodane diterpenoids, scutecyprol A (1) and scutalbin C (2), have been isolated from the acetone extract of the aerial parts of Scutellaria sieberi. The antifeedant activity of scutecyprol A (1), of its 15-oxo derivative (3), and of several halohydrins (4-9), synthesized starting from compounds 1 and 3, against Spodoptera littoralis have been determined and structure-antifeedant relationships are discussed.

InsecticidesbiologyScutellaria sieberiScutalbin CStereochemistryScutellariaGeneral ChemistryhalohydrinSpodoptera littoralisSpodopterabiology.organism_classificationantifeedant activityDiterpenes ClerodaneLepidoptera genitaliachemistry.chemical_compoundchemistryAcetoneNoctuidaeAnimalsscutecyprol ASettore BIO/15 - Biologia FarmaceuticaScutellaria sieberiGeneral Agricultural and Biological SciencesSpodoptera littoralis
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Neoclerodanes from Teucrium orientale

2004

Abstract Two new neoclerodane diterpenoids, 6-deacetyl-teucrolivin A (5) and 8beta-hydroxy-teucrolivin B (6), were isolated from the aerial parts of Teucrium orientale, along with four already known neoclerodane diterpenoids, teucrolivin A (1), teucrolivin B (2), teucrolivin C (3) and teucrolivin H (4), previously isolated from Teucrium oliverianum. Their structures were elucidated on the basis of spectroscopic evidence and chemical transformations. Compounds 1-3 were assayed for antifeedant activity against Spodoptera littoralis, S. frugiperda and Heliocoverpa armigera. Teucrolivin A was the most potent of the three compounds tested.

LamiaceaeMagnetic Resonance SpectroscopyLamiaceae Teucrium orientale structure elucidation neo-clerodane diterpenoid antifeedant activityTraditional medicinebiologyStereochemistryChemistryMolecular ConformationTeucrium oliverianumGeneral ChemistryFeeding BehaviorGeneral MedicineSettore CHIM/06 - Chimica OrganicaSpodopterabiology.organism_classificationDiterpenes ClerodaneTerpeneLarvaDrug DiscoveryTeucrium orientaleAnimalsLamiaceaeChromatography Thin LayerSettore BIO/15 - Biologia FarmaceuticaSpodoptera littoralis
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La aplicación de las reformas tridentinas en Sicilia: las fronteras jurisdiccionales

2016

Tema dell'articolo è il problema dell’applicazione delle riforme tridentine sulla chiesa siciliana in relazione al peculiare assetto giurisdizionale del Regno, gravitante sul privilegio della Legazia Apostolica e sul foro che ne tutelava l’osservanza, il Tribunale della Regia Monarchia. Riorganizzato nel suo funzionamento e struttura tra il 1579 e il 1583, esso godeva di una giurisdizione superiore agli stessi canoni tridentini e, come ultima istanza di giudizio per gli ecclesiastici dell’isola, poteva ribaltare le sentenze o annullare i provvedimenti emanati dai tribunali episcopali nei confronti di chierici e religiosi “indisciplinati” o colpevoli dei più vari reati. Le testimonianze coev…

Settore M-STO/07 - Storia Del Cristianesimo E Delle ChieseConcilio di Trento giurisdizione ecclesiastica disciplina del clero SiciliaCouncil of Trent Ecclesiastical jurisdictions Clergy discipline SicilySettore M-STO/02 - Storia Moderna
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L'incardinazione dei chierici nella legislazione italiana di derivazione pattizia: con particolare riferimento alle norme sul sostentamento

2006

Sostentamento del cleroIncardinazioneTitulum beneficii
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