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From Drugs to Catalysts: Application of Boron Heterocycles

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From Drugs to Catalysts: Application of Boron Heterocycles
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34
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CC Attribution 4.0 International:
You are free to use, adapt and copy, distribute and transmit the work or content in adapted or unchanged form for any legal purpose as long as the work is attributed to the author in the manner specified by the author or licensor.
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Production Year2025
Production PlaceFrankfurt am Main

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Abstract
The advent of benzoxaborole drugs sparked a renaissance surrounding heterocycles derived from boronic acids in organic and medicinal chemistry, where they demonstrate a wide range of biological properties. Our recent studies addressed unanswered questions regarding the physical properties, acidic nature (Lewis vs Brønsted), dynamic behavior, and reactivity of boranol (B–OH)-containing heterocycles in organic and aqueous media. These fundamental studies are essential for guiding a systematic application of select heterocycles as enantioselective reaction catalysts, in bioconjugation, and as new antimicrobial drug chemotypes and bioisosteres of pharmaceutically important classes of heterocycles. Ongoing investigations focus on new boroheterocyclic chemotypes and the exchangeability of B–OH bonds for direct catalytic activation of alcohols and diols.
Keywords
BoronPharmaceutical drugChemistryReactivity (chemistry)CarboxylateLysergic acid diethylamideCarbonateFunctional groupSulfonamide (medicine)UreaSalt (chemistry)AmmoniumAmineOximeSulfatePermaculturePeroxideNitriteMetalThioamideHydrazineSulfoniumverbindungenElectric currentExploitation of natural resourcesLewisiteCovalent bondLigandIonenbindungMeat analogueRNAInhibitorAcidCoordination complexKohlenhydratchemieAntibacterialPatentGesundheitsstörungProteinNucleotideFrictionGrowth mediumAqueous solutionChelatbildungChemical bondCell membraneEnzymeCoordination numberTetraederstrukturDewar benzeneBioisostereAromaticityGrammatical conjugationReactivity (chemistry)TopicityChemical reactionHeterocyclic compoundFunctional groupArzneimittelforschungHybridisierung <Chemie>IsosterieDerivative (chemistry)BortezomibChemistChemical elementBoronLysergic acid diethylamideCarbon (fiber)SulfurHydroxylIonenbindungChemical compoundChelatbildungNucleotideDoppelbindungWaterTransfer RNAPharmaceutical drugCovalent bondThermoformingActive siteSide chainMoleculeEnzymeChemische BiologieOxideHydrogen bondDehydration reactionProtein biosynthesisLeft-wing politicsElektronenakzeptorElectron donorInhibitorMeat analogueFood additiveBoronsäurenMetalBase (chemistry)Neutralization (chemistry)Coordination numberChemical structureAntibacterialAbbruchreaktionZincMagnesiumBinding energyConjugated systemSerineAdductStarvation responseEnzyme inhibitorElectronResonance (chemistry)Proteinkinase AChemical propertySeparation processNeotenyWursthülleSteroidIsochinolinMethylgruppeAddition reactionGeneMolecularitySweetnessMeeting/InterviewComputer animation
Grammatical conjugationAromaticityAlkeneChemische VerschiebungKernproteineHomocysteineQuinineChemical bondChemistryAcidLewisiteTitrationNuclear magnetic resonanceAcetonitrilePharmaceutical drugCollectingWater purificationYield (engineering)Library (computing)Transformation <Genetik>Screening (medicine)BiosynthesisCrystallizationPosttranslational modificationArzneimittelforschungBoronsäurenChemische VerschiebungSetzen <Verfahrenstechnik>Base (chemistry)KupplungsreaktionX-ray crystallographyHeterocyclic compoundChemical compoundAromaticityPlant breedingArylHydroxylCollectingAnilinePhenyl groupCondensationHydrocarboxylierungAminationPrecursor (chemistry)Lysergic acid diethylamideFood additiveIonenbindungHydrazinePosttranslational modificationCovalent bondAldehydeLibrary (computing)Action potentialCarbon (fiber)Multiprotein complexStickstoffatomConjugated systemProteinkinase AQuinolineHybridisierung <Chemie>TiermodellWaterCalculus (medicine)GesundheitsstörungBenzodiazepineIsosterieCoordination numberHyperpolarisierungBoronChemical reactionEtherChemische SyntheseFunctional groupCobaltoxideEnzyme inhibitorAlcoholHydrolysatChemical propertyTool steelDiolOxycodonProtonationBleitetraethylPreservativeComputer animation
Angiotensin II receptor antagonistKupplungsreaktionYield (engineering)Water purificationCrystallizationDioxaneSuzuki reactionBiosynthesisScreening (medicine)Library (computing)Transformation <Genetik>EtherAcylationPosttranslational modificationSilicon dioxidePhase (waves)High-performance liquid chromatographyFunctional groupTachyphylaxieChemical bondChemistryChemical compoundMinimale HemmkonzentrationFluconazolePhenyl groupPinacolWaterPhenolBenzodiazepineBenzeneHydroxylPyridineCondensationHydrazineAlcoholZunderbeständigkeitIsomerDehydration reactionAcetonitrileArylDisinfectantAgriculturePharmaceutical drugGesundheitsstörungAromaticityPharmacyAtomWine tasting descriptorsActivation energyLysergic acid diethylamideMitsunobu-ReaktionSubstitutionsreaktionChemistrySetzen <Verfahrenstechnik>CobaltoxideArzneimittelforschungCondensationStarvation responseIsosterieChemical compoundCollectingAtomic orbitalPhenyl groupActivity (UML)Minimale HemmkonzentrationLysergic acid diethylamideAction potentialScreening (medicine)Sense DistrictWursthülleBenzodiazepineLeft-wing politicsDerivative (chemistry)IonenbindungHydroxylFunctional groupTopicityBlock (periodic table)AldehydeAldehydeIsomerCycloadditionHydroborierungHydrazineElectronMoleculeProteinkinase ASteppenschwarzerdeSunscreenSpeciesElectronegativityBioisostereAlcoholChemical propertyAlkyneMulti-component reactionProtein biosynthesisHeterocyclic compoundZunderbeständigkeitSeparation processArylCyclische VerbindungenStickstoffatomElectronic cigarettePyridineProcess (computing)BoronCarboxylateHydrogen bondNaturstoffAlkaneChemical reactionVinyletherComputer animation
PharmacyAtomChemistryWine tasting descriptorsMitsunobu-ReaktionActivation energyHydroxylFunctional groupLysergic acid diethylamideSubstitutionsreaktionKupplungsreaktionEphedrineCyclooxygenaseEnzyme inhibitorIndometacinAldehydeEnolAlcoholChemical reactionEnantiomereMetalHalideCarboxylateAcidRearrangement reactionScaffold <Biologie>Modul <Membranverfahren>GesundheitsstörungRapidPhosphorylationReactivity (chemistry)PolyoleStoichiometryNuclear magnetic resonanceCell cyclePhosphateInositolSynthetic oilMüllerinAcetonitrileThyminMethanolClindamycinDiolTolueneLewisiteBase (chemistry)MeatTransition metalGreen chemistryBoronsäurenChemische VerschiebungSubstrat <Chemie>Anomalie <Medizin>Golgi apparatusAreaEtomidateProteinkinase AAlcoholAnimal trappingWine tasting descriptorsCarbokationLysergic acid diethylamideSilanesPhosphateScaffold <Biologie>Systemic therapyClindamycinFunctional groupPolyolePhosphorylationYield (engineering)AlcoholChemical reactionActivity (UML)BoronNitrileElectronEssigCobaltoxideWalkingRearrangement reactionAddition reactionStarvation responseTolueneAryl halideCovalent bondArylTransition metalKupplungsreaktionBase (chemistry)SpeciesKetoneBenzylSchutzgruppeEthylgruppeDerivative (chemistry)GesundheitsstörungNucleosideKohlenhydratchemieCell cycleWursthülleNuclear magnetic resonanceDiolLactitolAcidMoleculeChromatographyAminationSulfoneBinding energyHalideSubstituentStereoselectivityCoordination complexCarboxylateBiosynthesisThermoformingMolekularsiebReducing agentCarboxylierungAction potentialSetzen <Verfahrenstechnik>By-productAnilineComputer animation
ElectronChemical structureAcetonitrileDiolMultiprotein complexAlcoholPhosphorylationReduction potentialTolueneKohlenstoff-14Lysergic acid diethylamideBase (chemistry)RedoxSpaltflächeChiralität <Chemie>AcidEnantiomereChemistryMethanolFunctional groupYield (engineering)Substrat <Chemie>AlcoholCoordination complexChemical bondBioisostereLewisiteAromaticityChemical compoundHeteroatomChemical reactionCombine harvesterBoronPyrrolidineChemical propertyStarvation responsePaste (rheology)Proteinkinase AErdrutschReactivity (chemistry)IminiumsalzeKetoneSilanesConcentrateArylStickstoffatomActivity (UML)Sea levelBoronsäurenHeterocyclic compoundMetalFunctional groupNaphthalinDiolDerivative (chemistry)Precursor (chemistry)IonenbindungMultiprotein complexTiermodellGesundheitsstörungYield (engineering)CobaltoxideStereoselectivityThermoformingAddition reactionProcess (computing)EnantiomereErosionChemistrySpeciesConformational isomerismOxideAminationPhosphorylationNahtoderfahrungLysergic acid diethylamidePowdered milkChemical formulaIce frontReducing agentNeutralization (chemistry)Benzyl bromideTachyphylaxieAxiale ChiralitätAllyl alcoholBenzyl alcoholHydroxylCarbon (fiber)Chemical structureConjugated systemWalkingQuaternary ammonium cationChiralität <Chemie>UreaCondensationComputer animation
High-performance liquid chromatographyGermanic peoplesGreen chemistryFunctional groupPaste (rheology)Computer animation
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