about
Structure-guided discovery of the metabolite carboxy-SAM that modulates tRNA functionUV-visible and (1)H-(15)N NMR spectroscopic studies of colorimetric thiosemicarbazide anion sensors.First ever observation of the intermediate of phosphonium salt and ylide hydrolysis: P-hydroxytetraorganophosphorane.Zn(2+)-induced deprotonation of a peptide nitrogen in angiotensin I.The Mechanism of Phosphonium Ylide Alcoholysis and Hydrolysis: Concerted Addition of the O-H Bond Across the P=C Bond.Synthesis and anion binding studies of tris(3-aminopropyl)amine-based tripodal urea and thiourea receptors: Proton transfer-induced selectivity for hydrogen sulfate over sulfate.Aryl C-H···Cl(-) hydrogen bonding in a fluorescent anion sensorChemo- and regioselective C(sp³)-H arylation of unactivated allylarenes by deprotonative cross-couplingThe stimulating adventure of KRN 7000.Enhancement of the rate of pyrophosphate hydrolysis by nonenzymatic catalysts and by inorganic pyrophosphatase.Zinc complexes of Ttz(R,Me) with O and S donors reveal differences between Tp and Ttz ligands: acid stability and binding to H or an additional metal (Ttz(R,Me) = tris(3-R-5-methyl-1,2,4-triazolyl)borate; R = Ph, tBu).Biomimetic macrocyclic receptors for carboxylate anion recognition based on C-linked peptidocalix[4]arenesA concise synthesis of (+)-batzelladine B from simple pyrrole-based starting materials.Migratory decarboxylative coupling of coumarins: synthetic and mechanistic aspects.Dual Catalytic Decarboxylative Allylations of α-Amino Acids and Their Divergent MechanismsChemoselective Palladium-Catalyzed Deprotonative Arylation/[1,2]-Wittig Rearrangement of Pyridylmethyl Ethers.Palladium-Catalyzed Asymmetric Allylic Alkylations with Toluene Derivatives as PronucleophilesNickel-Catalyzed Arylation of Heteroaryl-containing Diarylmethanes: Exceptional Reactivity of the Ni(NIXANTPHOS)-based Catalyst.The change in hydrogen bond strength accompanying charge rearrangement: implications for enzymatic catalysis.Palladium Catalysis Enables Benzylation of α,α-Difluoroketone EnolatesFe-N2/CO complexes that model a possible role for the interstitial C atom of FeMo-cofactor (FeMoco).Stepwise N-H Bond Formation From N2-Derived Iron Nitride, Imide and Amide Intermediates to Ammonia.Palladium-Catalyzed α-Arylation of Methyl Sulfonamides with Aryl Chlorides.Epimerization and substrate gating by a TE domain in β-lactam antibiotic biosynthesis.A biodegradable thermoset polymer made by esterification of citric acid and glycerol.Radical Reactivity of the Fe(III)/(II) Tetramesitylporphyrin Couple: Hydrogen Atom Transfer, Oxyl Radical Dissociation, and Catalytic Disproportionation of a HydroxylamineBeyond ferryl-mediated hydroxylation: 40 years of the rebound mechanism and C-H activation.A General and Practical Palladium-Catalyzed Direct α-Arylation of Amides with Aryl Halides.Role of metal-oxo complexes in the cleavage of C-H bonds.Transition metal-catalyzed arylation of unactivated C(sp3)-H bonds.Brønsted acidity and the medium: fundamentals with a focus on ionic liquids.An evaluation of peptide-bond isosteres.Increasing the reactivity of nitrogen catalysts.Recent advances in transition metal-catalyzed enantioselective hydrogenation of unprotected enamines.Ionic liquid thermal stabilities: decomposition mechanisms and analysis tools.The cross-dehydrogenative coupling of C(sp3)-H bonds: a versatile strategy for C-C bond formations.Beyond click chemistry - supramolecular interactions of 1,2,3-triazoles.The protoelectric potential map (PPM): an absolute two-dimensional chemical potential scale for a global understanding of chemistry.Cyanoalkylation: Alkylnitriles in Catalytic C-C Bond-Forming Reactions.Coordination chemistry and applications of versatile 4,5-diazafluorene derivatives.
P2860
Q27678153-653C1DC8-FF5F-466E-A5EE-C74353077C45Q30873138-D5659107-E004-40AF-B506-1D70B40A39F3Q30873958-B2A69708-E8A2-4983-A47D-C5570F47FC0CQ31034525-6E47FA7A-2681-4CB7-832F-587B84BAFD87Q31106194-C24C3B1C-1C3F-42E4-86A7-853C5B0C9902Q31160828-389E6A72-EC2C-4FD4-BF59-0C9944662406Q33576332-3128FD10-4C4A-40E6-8E8A-ADEB51C30B04Q33684516-ED55EA7F-4167-4AD6-81A4-E9A0C0EEE2CAQ33843406-30AC927D-C725-408F-AF0B-0EFD352E125BQ33861183-1C8D1C48-0875-4249-AD00-677394FA1B6CQ33943339-FF6E4B66-CD5A-4D11-BA34-381499A65993Q34022317-4CE7845D-1F90-40C2-AC77-764D38E02A25Q36093866-F584DFBF-27C2-4965-8EE4-1434BC475E24Q36464543-82C5AD6F-64E1-4634-99DE-0C8745EB1C7DQ36470367-C08E875F-83D4-4F0A-BD13-BAAE661FE41CQ36707800-A7A818F0-24FC-46B6-B148-DCCFCBAA17B1Q36813079-0BC70933-78F4-4A8F-B94B-135AF814E326Q36908251-5FCA353F-4265-4024-A002-6C97F54AE5FCQ37042065-03A6EFC4-3628-427A-8E6D-D34C0B18D6CAQ37149239-2796726B-1C3A-4297-BA36-714B1EC3B8E9Q37218477-78FE6A3C-B19E-4931-8268-90C428AA2EFBQ37551496-38F29222-7D17-40F8-AD30-0D8E6050BED8Q37568328-125C03F1-28EE-43B7-A841-329AC25A9890Q37652993-C9529407-7EB4-406C-9FE5-9785B206F749Q37678237-2D3F9056-9BA5-476E-AF17-A43D2677C699Q37694776-B594BA16-68DC-44C0-91A0-0B14B383AEFBQ37699790-FA53E415-6392-4F8A-B20F-0B17E15D2298Q37714497-C3C3C8CD-0211-4AA2-9004-C191ED81FEF2Q37848679-4EF176E8-D671-4E03-8DEA-CB23D3E079CAQ37867002-177FDBD1-EC2D-4515-8884-91DEC54759D7Q37883994-8A2BCD54-22A5-44AC-AC6C-CB83355FAA05Q37900560-A289A2D5-D81C-41CD-955D-2BDC038921B2Q37947516-1CEA5125-4381-4BF1-9AC6-0DA359BE6E59Q38003160-3FF40961-6788-4364-A279-9B003402F734Q38100074-FA6CA2AC-F530-41F3-80FE-BDA19E3D780AQ38161496-E1BA6483-2DF7-40A0-8F6A-706590059D94Q38184880-277B43BD-230B-48AB-B995-9816A16C89FBQ38194979-B6425A08-4D6A-4A2B-B40B-D3D32440A1C8Q38589856-BF97D8DF-35B1-4B7A-94EA-0F456D24EA8EQ38654061-DD2985B6-2569-43E4-9800-19E49308643B
P2860
description
im Dezember 1988 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 1988
@uk
name
Equilibrium acidities in dimethyl sulfoxide solution
@en
Equilibrium acidities in dimethyl sulfoxide solution
@nl
type
label
Equilibrium acidities in dimethyl sulfoxide solution
@en
Equilibrium acidities in dimethyl sulfoxide solution
@nl
prefLabel
Equilibrium acidities in dimethyl sulfoxide solution
@en
Equilibrium acidities in dimethyl sulfoxide solution
@nl
P356
P1476
Equilibrium acidities in dimethyl sulfoxide solution
@en
P2093
Frederick G. Bordwell
P304
P356
10.1021/AR00156A004
P407
P577
1988-12-01T00:00:00Z