Search results for "total synthesis"

showing 10 items of 111 documents

Cover Feature: Total Synthesis of a Partial Structure from Arabinogalactan and Its Application for Allergy Prevention (Chem. Eur. J. 3/2021)

2020

Allergy preventionChemistryFeature (computer vision)ArabinogalactanOrganic ChemistryAirway inflammationTotal synthesisCover (algebra)General ChemistryComputational biologyCatalysisChemistry – A European Journal
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Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine

2008

The first total synthesis of the naturally occurring dihydropyranone dodoneine is reported. Asymmetric allylation reactions were used for the stereoselective generation of the two stereogenic centers. The pyranone ring was created by ring-closing metathesis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

AllylationStereochemistryChemistryOrganic ChemistryEnantioselective synthesisTotal synthesisAsymmetric synthesisRing (chemistry)Metathesis56-Dihydropyran-2-onesStereocenterDodoneineRing-closing metathesisOxygen heterocyclesStereoselectivityRing-closing metathesisPhysical and Theoretical Chemistry
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ChemInform Abstract: Total Synthesis of the Antifungal Natural Product Mollisin.

2014

The title compound is synthesized in nine steps from commercially available 2,6-dimethyl-γ-pyrone in an overall yield of 9%.

Antifungalchemistry.chemical_compoundNatural productchemistrymedicine.drug_classYield (chemistry)medicineOrganic chemistryTotal synthesisGeneral MedicineChemInform
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First total synthesis of antiostatin A1, a potent carbazole-based naturally occurring antioxidant.

2009

The first total synthesis of the potent antioxidant antiostatin A1 is reported, where its key features rely on a chemo- and regioselective rhodium-catalysed crossed alkyne cyclotrimerisation reaction applying functionalised ynamides and a palladium-catalysed arylamidation reaction.

Antioxidantmedicine.medical_treatmentCarbazolesAlkyneAntioxidantsCatalysischemistry.chemical_compoundAntiostatin A1Materials ChemistrymedicineOrganic chemistryRhodiumchemistry.chemical_classificationMolecular StructureCarbazoleMetals and AlloysTotal synthesisRegioselectivityStereoisomerismGeneral ChemistryKey featuresSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCyclizationCeramics and CompositesPalladiumChemical communications (Cambridge, England)
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Total Synthesis and Biological Investigation of (−)‐Artemisinin: The Antimalarial Activity of Artemisinin Is not Stereospecific

2018

Here, we describe an efficient and diversity-oriented entry to both (-)-artemisinin (1) and its natural antipode (+)-artemisinin, starting from commercially and readily available S-(+)- and R-(-)-citronellene, respectively. Subsequently, we answered the still open question regarding the specificity of artemisinins action. By using a drug-sensitive Plasmodium falciparum NF54 strain, we showed that the antimalarial activity of artemisinin is not stereospecific. Our straightforward and biomimetic approach to this natural endoperoxide enables the synthesis of artemisinin derivatives that are not accessible through applying current methods and may help to address the problem of emerging resistan…

ArtemisininsCell SurvivalPlasmodium falciparum010402 general chemistry01 natural sciencesCatalysisAntimalarialsStereospecificityCell Line Tumorparasitic diseasesmedicineHumansArtemisininbiology010405 organic chemistryChemistryTotal synthesisStereoisomerismPlasmodium falciparumGeneral Chemistrybiology.organism_classificationCombinatorial chemistryArtemisinins0104 chemical sciencesCyclizationDrug Resistance NeoplasmMonoterpenesmedicine.drugAngewandte Chemie International Edition
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Friedel-Crafts Alkylation of Arenes in Total Synthesis

2015

Cascade reactionChemistryTotal synthesisOrganic chemistryFriedel–Crafts reaction
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ChemInform Abstract: Organocatalytic Approach to Benzofused Nitrogen-Containing Heterocycles: Enantioselective Total Synthesis of (+)-Angustureine.

2009

ChemistryEnantioselective synthesisOrganic chemistryTotal synthesischemistry.chemical_elementAngustureineGeneral MedicineNitrogenChemInform
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Classics in Total Synthesis. Targets, Strategies, Methods. VonK. C. Nicolaou und E. J. Sorensen. VCH, Weinheim, 1996. 798 S., geb./ Broschur 128.00 D…

1996

ChemistryStereochemistryTotal synthesisGeneral MedicineAngewandte Chemie
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Total Synthesis of (±)-Oxalicumone C and Chiral Resolution and Elucidation of Its Absolute Configuration

2014

The racemic total synthesis, the chiral resolution, and the elucidation of the absolute configuration of the natural product oxalicumone C were investigated. The goal was achieved by a synthetic strategy beginning with the synthesis of a 5-hydroxy-7-methylchromone precursor. Further modification possibilities were achieved by introduction of a vinyl moiety into the chromone, which was based on a selective iodination step in the 3-position. Further transformations furnished the racemic natural product. To determinate the absolute configuration of naturally occurring oxalicumone C, both enantiomers were separated by chiral HPLC. Comparison of the calculated and experimental vibrational circul…

Chiral column chromatographyCircular dichroismChemistryStereochemistryOrganic ChemistryVibrational circular dichroismAbsolute configurationTotal synthesisPhysical and Theoretical ChemistryEnantiomerChiral derivatizing agentChiral resolutionEuropean Journal of Organic Chemistry
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Making natural products from renewable feedstocks: back to the roots?

2019

Covering: up to mid-2019 This review highlights the utilization of biomass-derived building blocks in the total synthesis of natural products. An overview over several renewable feedstock classes, namely wood/lignin, cellulose, chitin and chitosan, fats and oils, as well as terpenes, is given, covering the time span from the initial beginning of natural product synthesis until today. The focus is put on the origin of the employed carbon atoms and on the nature of the complex structures that were assembled therefrom. The emerging trend of turning away from petrochemically derived starting materials back to bio-based resources, just as seen in the early days of total synthesis, shall be demon…

ChitinRaw material010402 general chemistryLignin01 natural sciencesBiochemistryNatural (archaeology)chemistry.chemical_compoundDrug DiscoveryLigninBiomassCelluloseCelluloseBiological ProductsChitosanTerpenes010405 organic chemistrybusiness.industryOrganic ChemistryTotal synthesisGreen Chemistry TechnologyPulp and paper industryWoodCarbon0104 chemical sciencesRenewable energychemistryEnvironmental sciencebusinessOilsNatural Product Reports
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