Search results for "Cyclopentane"

showing 6 items of 76 documents

ChemInform Abstract: Solution and Fluorous Phase Synthesis of β,β-Difluorinated 1-Amino-1-cyclopentane Carboxylic Acid Derivatives.

2009

An efficient protocol for the preparation of β,β-difluorinated 1-amino-1-cyclopentane carboxylic acid derivatives was developed. 2,2-Difluro-4-phenyl-3-butenoic acid 6 was used as substrate for the preparation of the starting vinyl difluoro imino esters 8. The key steps of this methodology rely on the chemo- and diastereoselective addition of allylzinc bromides over the iminic functionality of 8 and subsequent RCM reaction. This synthetic sequence was successfully applied to fluorous synthesis.

chemistry.chemical_classificationchemistry.chemical_compoundChemistryCarboxylic acidSalt metathesis reactionSubstrate (chemistry)Organic chemistrySequence (biology)General MedicineCyclopentaneCombinatorial chemistryPhase synthesisChemInform
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Back Cover: Chemoselective, Substrate-directed Fluorination of Functionalized Cyclopentane β-Amino Acids (Chem. Asian J. 23/2016)

2016

chemistry.chemical_classificationchemistry.chemical_compoundchemistryStereochemistryOrganic ChemistryPolymer chemistryFluorineSubstrate (chemistry)chemistry.chemical_elementGeneral ChemistryCyclopentaneBiochemistryAmino acidChemistry - An Asian Journal
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An Insight into Substrate-Dependent Fluorination of some Highly Substituted Alicyclic Scaffolds

2017

The substrate-dependent fluorination of some highly-functionalized cyclopentane derivatives with multiple chiral centers has been investigated. The key steps of the stereocontrolled syntheses are the oxidative cleavage of the ring carbon–carbon double bond of readily available diexo or diendo norbornene β-amino acid derivatives followed by transformation of the resulted dialdehyde stereoisomers by reduction. Finally, substrate-directable chemodifferentiation of different types of hydroxy groups under fluorination procedures gave various densely functionalized alicyclic derivatives or heterocycles.

chemistry.chemical_classificationheterocyclescyclizationDouble bond010405 organic chemistrySubstrate (chemistry)chemistry.chemical_elementGeneral Chemistryaminohapot010402 general chemistryRing (chemistry)01 natural scienceslactones0104 chemical sciencesAmino acidchemistry.chemical_compoundAlicyclic compoundchemistryfluorineamiamino acidsFluorineOrganic chemistryCyclopentaneta116NorborneneChemistrySelect
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Differentiation of isomeric cyclic diamides by electron impact mass spectra

1976

The behaviour under electron impact of two series of isomeric cyclopentane- and cyclohexane-1, 2- and -1, 3-dicarboxylic acid dipiperidides was studied. Diagnostic fragmentation pathways were found to differentiate the isomeric diamides. Additional evidence was obtained from the metastable transitions.

chemistry.chemical_compoundFragmentation (mass spectrometry)chemistryComputational chemistryMetastabilityMass spectrumAnalytical chemistryMolecular MedicineCyclopentaneInstrumentationBiochemistrySpectroscopyElectron ionizationOrganic Mass Spectrometry
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Role of dioxygenase α-DOX2 and SA in basal response and in hexanoic acid-induced resistance of tomato (Solanum lycopersicum) plants against Botrytis …

2015

Resistance of tomato (Solanum Lycopersicum) to the fungal pathogen Botrytis cinerea requires complex interplay between hormonal signalling. In this study, we explored the involvement of new oxylipins in the tomato basal and induced response to this necrotroph through the functional analysis of the tomato α-dioxygenase2 (α-DOX2)-deficient mutant divaricata. We also investigated the role of SA in the defence response against this necrotrophic fungus using SA-deficient tomato nahG plants. The plants lacking dioxigenase α-DOX2, which catalyses oxylipins production from fatty acids, were more susceptible to Botrytis, and hexanoic acid-induced resistance (Hx-IR) was impaired; hence α-DOX2 is requ…

food.ingredientDioxygenasePhysiologyDefence mechanismsPlant ScienceCyclopentanesMicrobiologyDioxygenasesBotrytis cinereachemistry.chemical_compoundfoodSolanum lycopersicumPlant Growth RegulatorsGene Expression Regulation PlantOxylipinsCaproatesGlucansBotrytis cinereaBotrytisDisease ResistancePlant DiseasesPlant ProteinsHexanoic acidbiologyJasmonic acidfungiCallosefood and beveragesSalicylic acidbiology.organism_classificationchemistryBiochemistryFatty Acids UnsaturatedBotrytisSolanumHexanoic acidReactive Oxygen SpeciesSalicylic AcidAgronomy and Crop ScienceSalicylic acidJournal of plant physiology
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Chemoselective, Substrate-directed Fluorination of Functionalized Cyclopentane β-Amino Acids

2016

This work describes a substrate-directed fluorination of some highly functionalized cyclopentane derivatives. The cyclic products incorporating CH2 F or CHF2 moieties in their structure have been synthesized from diexo- or diendo-norbornene β-amino acids following a stereocontrolled strategy. The synthetic study was based on an oxidative transformation of the ring carbon-carbon double bond of the norbornene β-amino acids, followed by transformation of the resulted "all cis" and "trans" diformyl intermediates by fluorination with "chemodifferentiation".

molecular diversitycyclizationDouble bondHalogenationHydrocarbons FluorinatedStereochemistryMolecular Conformationchemistry.chemical_elementCyclopentanes010402 general chemistryRing (chemistry)Crystallography X-Ray01 natural sciencesBiochemistrychemistry.chemical_compoundfluorineCyclopentaneta116Norbornenechemistry.chemical_classificationamino acidssubstituent effects010405 organic chemistryOrganic ChemistrySubstrate (chemistry)StereoisomerismGeneral Chemistry0104 chemical sciencesAmino acidchemistryFluorineOxidation-ReductionChemistry: An Asian Journal
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