0000000000521709

AUTHOR

Salvatore Passannanti

showing 26 related works from this author

Diterpenoids fromStachys mucronata

1994

PharmacologyComplementary and alternative medicineTraditional medicineOrganic ChemistryDrug DiscoveryBotanyStachys mucronataPharmaceutical ScienceMolecular MedicineBiologyAnalytical ChemistryPlanta Medica
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Chimica dalla H alla Z. Edizione BLU - Volume BLU Dai fenomeni alle soluzioni, 1° Biennio

2019

Chimica Scuola secondaria licei
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Comparison of the volatile oils ofHypericum scabrum L. andHypericum perforatum L. from Turkey

1997

The composition of the volatile oils obtained from the aerial parts of Hypericum scabrum L. and H. perforatum L. was analysed by GC and GC‐MS. While the oil of H. scabrum L. contained a-pinene (71.6%), b-caryophyllene (4.8%), myrcene (3.8%), cadalene (3.4%) and b-pinene (2.9%), the oil of H. perforatum L. contained a-pinene (61.7%), 3-carene (7.5%), b-caryophyllene (5.5%), myrcene (3.6%), cadalene (3.2%) and other components. Twenty-nine and 27 terpenoid compounds have been identified in the volatile oils of H. scabrum L. and H. perforatum L., respectively. #1997 by John Wiley & Sons, Ltd.

Traditional medicineChemistryHypericum perforatumGeneral Chemistry?-pinene; GC-MS; Guttiferae; Hypericum perforatum L; Hypericum scabrum L; Volatile oil compositionTerpenoidchemistry.chemical_compoundMyrceneBotanyGas chromatographyHypericum scabrumGas chromatography–mass spectrometryCadaleneFood ScienceFlavour and Fragrance Journal
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Sesquiterpene compounds from Inula Viscosa

2007

Two new compounds, 2,5-dihydroxyisocostic acid and 2,3-dihydroxycostic acid together with three known sesquiterpene compounds, Isocostic acid, Carabrone and Tomentosin, have been isolated from the acetone extract of Inula viscosa (L.) Aiton. The structures of all new compounds were determined by spectroscopic methods, in particular 1D and 2D (1)H- and (13)C-NMR. The (13)C-NMR spectra of Isocostic acid and of Tomentosin are reported here for the first time.

inulaeMagnetic Resonance SpectroscopyInula viscosaMolecular StructureOrganic ChemistryPlant ScienceSesquiterpeneBiochemistryTomentosinAnalytical Chemistryinula viscosa (sin. dittrichia viscosa)chemistry.chemical_compoundchemistryItalycompositaesesquiterpenesBotanyAcetoneOrganic chemistryInula
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The synthesis of nareielasie aldehyde and related lsocarbostyrils

1977

The synthesis of several isoearboslyrils is reported, including lorrnyl derivatives at (1-4, like nareiclasie aldehyde (I) and the homologous aldehyde (XV).

chemistry.chemical_classificationStereochemistryChemistryOrganic Chemistrymacromolecular substancesAldehydeJournal of Heterocyclic Chemistry
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Isomotiol, a new triterpene from strychnos potatorum

1978

Isomotiol (fern-8-en-3β-ol) was isolated from the leaves of Strychnos potatorum; it was not known previously as a natural product, but it has been obtained by acidic isomerization of compounds with a fern-7-ene or a fern-9(11)-ene skeleton. From the leaves and the bark mixtures of sitosterol, stigmasterol and campesterol were also isolated.

chemistry.chemical_classificationStrychnos potatorumNatural productStigmasterolbiologyStereochemistryCampesterolPlant ScienceGeneral MedicineHorticulturebiology.organism_classificationBiochemistrychemistry.chemical_compoundchemistryTriterpenevisual_artvisual_art.visual_art_mediumOrganic chemistryBarkMolecular BiologyIsomerizationPhytochemistry
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Triterpenes from amaracus dictamnus

1986

Abstract From the aerial parts of Amaracus dictamnus several triterpenes were isolated: oleanolic and ursolic acids, uvaol, the rare 21α-hydroxyoleanolic acid and a new 21α-hydroxyursolic acid.

TerpeneTraditional medicinebiologyChemistryPlant ScienceGeneral MedicineHorticultureDictamnusbiology.organism_classificationMolecular BiologyBiochemistryPhytochemistry
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8 β-hydroxyfruticolone, a diterpenoid from Teucrium fruticans

1978

TeucriumTraditional medicinebiologyChemistryPlant ScienceGeneral MedicineHorticulturebiology.organism_classificationMolecular BiologyBiochemistryTerpenoidPhytochemistry
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Volatile flavour components of ocimum basilicum var. hispidum (lam.) Chiov.

1991

The volatile components obtained by steam-distillation ofOcimum basilicum var. hispidum (Lam.) Chiov. (Labiatae) were analysed by gas chromatography (GC) and gas chromatography—mass spectrometry (GC-MS). A total of 21 compounds, representing ca 90% of the total oil, were identified. The identity of the main component (82%), dihydrotagetone, was confirmed by 1H- and 13C-NMR spectroscopy. This is the first report of this compound in the genus Ocimum.

gas chromatography - mass spectrometryfood.ingredientbiologyChemistryFlavourBasilicumGeneral Chemistrypharmaceutical analysisOcimumbiology.organism_classificationNMRocimum basilicum var. hispidum (lam.) ChiovfoodBotanyocimum basilicum var. hispidum (lam.) Chiov.; pharmaceutical analysis; gas chromatography - mass spectrometry; NMRGas chromatographyFood Science
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A minor diterpene from Amaracus akhdarensis

1985

Abstract A new isopimarane diterpenoid, isoakhdartriol, was isolated in very small amount from the aerial part of Amaracus akhdarensis. Its structure, isopimar-15-en-3β,8β,19-triol, was established by spectroscopic means.

chemistry.chemical_compoundChemistryStereochemistryPlant ScienceGeneral MedicineHorticultureDiterpeneMolecular BiologyBiochemistryTerpenoidPhytochemistry
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Volatile Constituents ofTeucrium poliumL. from Turkey

1998

Abstract The volatile constituents obtained from the aerial parts of Teucrium polium were analyzed by GC and GC/MS. The oil was found to contain 37 components, of which 30 were identified. The major constituents were β-pinene (18.0%), β-caryophyllene (17.8%), α-pinene (12.0%), caryophyllene oxide (10.0%), myrcene (6.8%) and germacrene-D (5.3%)

chemistry.chemical_compoundfoodCaryophyllene oxideGermacreneChemistryMyrceneBotanyGeneral Chemistryβ caryophylleneGas chromatography–mass spectrometry?-pinene; ?-caryophyllene; ?-pinene; Caryophyllene oxide; Essential oil composition; GC/MS; Labiatae; Teucrium poliumTeucrium poliumfood.foodJournal of Essential Oil Research
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Kauranoid dieterpenes in Espeletia grandiflora

1971

Abstract The resin of Espeletia grandiflora contains (-)-kaur-16-en-19-ol, (-)-kaur-16-en-19-al (not previously isolated from natural sources), (-)-kaur-16-ene and (-)-kaur-16-en-19-oic acid.

BotanyPlant ScienceGeneral MedicineHorticultureBiologyMolecular BiologyBiochemistryEspeletia grandifloraPhytochemistry
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L'Avventura delle Scienze - Tomo B

2010

Scienze Scuola secondaria di primo grado
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Le scienze per crescere - Edizione per progetti

2004

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L'Avventura delle Scienze - Tomo C

2010

Scienza scuola secondaria di primo grado
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Noi e La Chimica - Dalle biomolecole al metabolismo

2011

Biochimica Scuola
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La Scoperta delle Scienze - 3

2010

Scienze scuola secondaria di primo grado
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La scoperta delle scienze - 2

2010

Scienze Scuola secondaria di primo grado
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L'avventura delle Scienze - Tomo D

2010

Scienze scuola secondaria di primo grado
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L'avventura delle Scienze - Tomo A

2010

Scienze Scuola secondaria di primo grado
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Il nuovo "la Materia"

2005

Un percorso di "scienza della materia" che si occupa dello studio dei fenomeni della materia non vivente e di tutte le trasformazioni che essa può subire.

Scienza della materia
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"Chimica Attiva"

2008

Un percorso di chimica che, prendendo spunto dall'osservazione dei fenomeni, si propone di offrire un'interpretazione della struttura della materia e delle sue trasformazioni

struttura della materia
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Chimica in Cucina

2014

Alimenti Chimica Scuola Didattica
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Noi e la chimica - Dalla biochimica alle nanotecnologie

2012

Biochimica Materiali Scuola
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La Scoperta delle Scienze - 1

2010

Scienze scuola secondaria di primo grado
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"L'avventura delle scienze"

2010

Un percorso completo di scienze naturali che intende fornire un "metodo per imparare". Il percorso cognitivo è facilitato dalla presenza di numerose espansioni online pensate per l'utilizzo della lavagna interattiva multimediale (LIM).

scienze naturali percorsi didattici
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