Research graph
References from Dynamic enantioselective high-performance liquid chromatography as a tool to probe configurational lability: Investigation of a chiral tetrahydrofuran building block. Local targets link to admitted publications; unresolved targets remain external evidence.
Opportunities for tapping into three-dimensional chemical space through a quaternary carbon
10.1021/acs.jmedchem.0c00829 · 2020 · External reference
Emerging building blocks for medicinal chemistry: recent synthetic advances
10.1002/ejoc.202100857 · 2021 · External reference
Recent advances in the asymmetric synthesis of pharmacology-relevant nitrogen heterocycles via stereoselective aza-Michael reactions
10.1039/c8ob03034k · 2019 · External reference
Nitrogen-containing heterocycles as significant molecular scaffolds for medicinal and other applications
10.3390/molecules26154617 · 2021 · External reference
Recent advances in N-heterocyclic small molecules for synthesis and application in direct fluorescence cell imaging
10.3390/molecules28020733 · 2023 · External reference
Amination of ethers using chloramine-T hydrate and a copper(I) catalyst
10.1039/b410883c · 2005 · External reference
α-Amidation of cyclic ethers catalyzed by simple copper salt and a mild and efficient preparation method of α,ω-amino alcohols
10.1021/ol070537i · 2007 · External reference
Heterogeneous copper-based catalysts for the amidation of activated C–H bonds
10.1016/j.catcom.2013.06.001 · 2013 · External reference
Metal-free amidation of ether sp³ C–H bonds with sulfonamides using PhI(OAc)₂
10.1039/c4ra09665g · 2014 · External reference
Metal-free amidation of ethers with N,N-dibromosulfonamides
10.1055/s-0035-1561373 · 2016 · External reference
Visible-light-promoted α-C(sp³)–H amidation of cyclic ethers under redox-neutral conditions
10.1021/acs.orglett.5c00337 · 2025 · External reference
Phosphorous acid-assisted electrochemical α-tetrahydrofuranylation of sulfonamides and amides
10.1039/d3gc00079f · 2023 · External reference
Electrochemical α-C(sp³)–H/N–H cross-coupling of isochromans and azoles
10.3390/molecules30010004 · 2025 · External reference
t-BuOK-induced, NH₃·MeOH-promoted electrochemical C(sp³)–H amination of saturated heterocycles with sulfoximines
10.1021/acs.orglett.5c02042 · 2025 · External reference
Diastereoselective palladaelectro-catalyzed construction of bromomethyl morpholines as key step to access morpholino homonucleosides
10.1021/acs.orglett.4c01790 · 2024 · External reference
Electrochemical intramolecular aminobromination of alkenes
10.1002/ejoc.202500808 · 2026 · External reference
Sustainable electrochemical synthesis of a new isoxazoline scaffold as turn inducer to build parallel β-hairpins
10.1039/d5ob01798j · 2026 · External reference
Direct functionalization of alkyl ethers to construct hemiaminal ether skeletons (HESs)
10.1039/c8ob00793d · 2018 · External reference
Automated R workflow for BATMAN peak fitting using a unified equation and stochastic modeling
10.1016/j.chroma.2025.466558 · 2026 · External reference
Comparison of dynamic HPLC and dynamic NMR in the study of conformational stereodynamics: case of the enantiomers of a hindered secondary phosphine oxide
10.1021/ja9941779 · 2000 · External reference
Conformational studies by dynamic NMR. 86. Structure, stereodynamics, and cryogenic enantioseparation of the stereolabile isomers of o-dinaphthylphenyl derivatives
10.1021/jo016397m · 2002 · External reference
Stereomutations of atropisomers of sterically hindered salophen ligands
10.1021/jo051367v · 2005 · External reference
Conformational studies by dynamic NMR. 89. Stereomutation and cryogenic enantioseparation of conformational antipodes of hindered aryl oximes
10.1021/jo0255431 · 2002 · External reference
High-performance liquid chromatographic separation of enantiomers and diastereomers of 2-methylcyclohexanone thiosemicarbazone, and determination of absolute configuration and configurational stability
10.1016/j.chroma.2007.10.009 · 2007 · External reference
Computer simulation of three scenarios for the separation of non-racemic mixtures by chromatography on achiral stationary phases
10.1016/0021-9673(92)85233-j · 1992 · External reference
A computer program for the determination of enantiomerization barriers in dynamic chromatography
10.1016/s0097-8485(00)00080-2 · 2001 · External reference
Dynamic HPLC on chiral stationary phases: a powerful tool for the investigation of stereomutation processes
10.1002/jssc.200600129 · 2006 · External reference
Kinetic processes and zone diffusion in chromatography
10.1016/s0021-9673(01)97028-1 · 1960 · External reference
Simultan-Reaktionsgaschromatographie mit reversibler Reaktion erster Ordnung. I
10.1016/0021-9673(75)80001-x · 1975 · External reference
Extending the scope of enantiomer resolution by complexation gas chromatography
10.1021/ja00390a031 · 1982 · External reference
Dynamic phenomena during enantiomer resolution by complexation gas chromatography: a kinetic study of enantiomerization
10.1016/s0021-9673(01)93677-5 · 1984 · External reference
Dynamic HPLC: a method for determining rate constants, energy barriers, and equilibrium constants of molecular dynamic processes
10.1002/anie.199100741 · 1991 · External reference
Determination of enantiomerization barriers by dynamic and stopped-flow chromatographic methods
10.1002/chir.1052 · 2001 · External reference
Unified equation for access to rate constants of first-order reactions in dynamic and on-column reaction chromatography
10.1021/ac051655r · 2006 · External reference
Enantiomerization kinetics studied by dynamic enantioselective liquid chromatography: solvent, temperature and stationary phase effects on the rate of N-benzyl-1,3,2-benzodithiazole 1-oxide enantiomer interconversion
10.1039/a904649f · 1999 · External reference
Stereolabile chiral compounds: analysis by dynamic chromatography and stopped-flow methods
10.1039/b502508g · 2005 · External reference
Determination of enantiomerization barriers by computer simulation of experimental elution profiles obtained by high-performance liquid chromatography on a chiral stationary phase
10.1016/0021-9673(95)01230-3 · 1996 · External reference
Chiroptical detection during liquid chromatography: deconvolution of overlapping peaks of enantiomers and its applications
10.1002/chir.10275 · 2003 · External reference
Transition-metal-free one-step synthesis of ynamides
10.1021/acs.joc.8b03192 · 2019 · External reference
Polysaccharide based chiral stationary phases for enantioseparation
2016 · External reference
Determination of enantiomerization barriers by computer simulation of experimental elution profiles obtained by high-performance liquid chromatography on a chiral stationary phase
10.1016/0021-9673(95)01230-3 · 1996 · External reference
Dynamic HPLC: a method for determining rate constants, energy barriers, and equilibrium constants of molecular dynamic processes
10.1002/anie.199100741 · 1991 · External reference
Stereolabile chiral compounds: analysis by dynamic chromatography and stopped flow methods
10.1039/b502508g · 2005 · External reference
Determination of the interconversion energy barrier of enantiomers by separation methods
10.1016/s0021-9673(03)00238-3 · 2003 · External reference
Determination of enantiomerization barriers by dynamic and stopped flow chromatographic methods
10.1002/chir.1052 · 2001 · External reference
Unified equation for access to rate constants of first order reactions in dynamic and on column reaction chromatography
10.1021/ac051655r · 2006 · External reference
Dynamic chromatography: a stochastic approach
10.1016/j.chroma.2009.10.036 · 2010 · External reference
Determination of the enantiomerization barrier of midazolam in aqueous conditions by electronic circular dichroilelesm and dynamic enantioselective HPLC/UHPLC
10.3390/molecules30051108 · 2025 · External reference
Cycloheptene based drugs endowed with potentially modulable planar chirality
10.1002/ejoc.202300568 · 2023 · External reference
Stereoselective HPLC separation and configurational stability study of the N-nitrosamine impurity of indapamide
10.1016/j.chroma.2025.466622 · 2026 · External reference
Kinetic and mechanism study of the spontaneous, solvent and base catalyzed degradation of the precursor of the β-nitro alcohol metaraminol by combining HPLC/electronic circular dichroism/theoretical methods
10.1016/j.jpba.2022.114972 · 2022 · External reference
