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Complete NMR assignment and conformational analysis of 17‐α‐ethinylestradiol by using RDCs obtained in grafted graphene oxide
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470034590.emrstm1194openalex-snapshot
Determining the Stereochemistry of Molecules from Residual Dipolar Couplings (RDCs)
inferredcites →https://doi.org/10.1002/ange.200461267openalex-snapshot
A DMSO‐Compatible Orienting Medium: Towards the Investigation of the Stereochemistry of Natural Products
inferredcites →https://doi.org/10.1002/ange.200705037openalex-snapshot
RDC‐Enhanced NMR Spectroscopy in Structure Elucidation of Sucro‐Neolambertellin
inferredcites →https://doi.org/10.1002/anie.200800225openalex-snapshot
Simultaneous Determination of the Conformation and Relative Configuration of Archazolide A by Using Nuclear Overhauser Effects, J Couplings, and Residual Dipolar Couplings
inferredcites →https://doi.org/10.1002/anie.201101739openalex-snapshot
Structural Discrimination in Small Molecules by Accurate Measurement of Long‐Range Proton–Carbon NMR Residual Dipolar Couplings
inferredcites →https://doi.org/10.1002/anie.201511435openalex-snapshot
An Alignment Medium for Measuring Residual Dipolar Couplings in Pure DMSO: Liquid Crystals from Graphene Oxide Grafted with Polymer Brushes
inferredcites →https://doi.org/10.1002/chem.200903378openalex-snapshot
Residual Dipolar Couplings (RDCs) Analysis of Small Molecules Made Easy: Fast and Tuneable Alignment by Reversible Compression/Relaxation of Reusable PMMA Gels
inferredcites →https://doi.org/10.1002/chem.201503449openalex-snapshot
Collection of NMR Scalar and Residual Dipolar Couplings Using a Single Experiment
inferredcites →https://doi.org/10.1002/mrc.1581openalex-snapshot
Comparison of 17β‐estradiol structures from x‐ray diffraction and solution NMR
inferredcites →https://doi.org/10.1002/mrc.3886openalex-snapshot
Chiral discrimination of amines by anisotropic NMR parameters using chiral polyacrylamide‐based gels
inferredcites →https://doi.org/10.1002/mrc.3889openalex-snapshot
Influence of solvent and salt concentration on the alignment properties of acrylamide copolymer gels for the measurement of RDC
inferredcites →https://doi.org/10.1002/mrc.3895openalex-snapshot
New strategy for RDC‐assisted diastereotopic proton assignment using a combination of J‐scaled BIRD HSQC and J‐scaled BIRD HMQC/HSQC
inferredcites →https://doi.org/10.1002/mrc.3905openalex-snapshot
MSpin‐RDC. A program for the use of residual dipolar couplings for structure elucidation of small molecules
inferredcites →https://doi.org/10.1016/0960-0760(94)90173-2openalex-snapshot
Molecular modeling of steroidal estrogens: Novel conformations and their role in biological activity
inferredcites →https://doi.org/10.1016/j.jmr.2004.03.007openalex-snapshot
Measurement of one-bond heteronuclear dipolar coupling contributions for amine and diastereotopic methylene protons
inferredcites →https://doi.org/10.1016/j.jmr.2011.09.037openalex-snapshot
More accurate 1JCH coupling measurement in the presence of 3JHH strong coupling in natural abundance
inferredcites →https://doi.org/10.1016/j.jmr.2012.01.008openalex-snapshot
Speeding up the measurement of one-bond scalar (1J) and residual dipolar couplings (1D) by using non-uniform sampling (NUS)
inferredcites →https://doi.org/10.1016/j.tetlet.2010.04.077openalex-snapshot
The conformations of 17β-estradiol (E2) and 17α-estradiol as determined by solution NMR
inferredcites →https://doi.org/10.1016/j.trac.2008.11.016openalex-snapshot
Residual dipolar couplings as a tool in determining the structure of organic molecules
inferredcites →https://doi.org/10.1016/s0009-2614(98)01201-9openalex-snapshot
Toward chemical accuracy in the computation of NMR shieldings: the PBE0 model
inferredcites →https://doi.org/10.1021/ct600166uopenalex-snapshot
The Basis Set Convergence of Spin−Spin Coupling Constants Calculated by Density Functional Methods
inferredcites →https://doi.org/10.1021/ja037605qopenalex-snapshot
Complete Relative Stereochemistry of Multiple Stereocenters Using Only Residual Dipolar Couplings
inferredcites →https://doi.org/10.1021/ja506074aopenalex-snapshot
Graphene Oxide Liquid Crystals as a Versatile and Tunable Alignment Medium for the Measurement of Residual Dipolar Couplings in Organic Solvents
inferredcites →https://doi.org/10.1021/jo020670iopenalex-snapshot
A Novel Method for the Determination of Stereochemistry in Six-Membered Chairlike Rings Using Residual Dipolar Couplings
inferredcites →https://doi.org/10.1021/jo902502hopenalex-snapshot
Conformational Analysis of an Isoquinolinium Hydrochloride in Water Using Residual Dipolar Couplings
inferredcites →https://doi.org/10.1021/ol0275163openalex-snapshot
Probing the Diastereotopicity of Methylene Protons in Strychnine Using Residual Dipolar Couplings
inferredcites →https://doi.org/10.1021/ol8029565openalex-snapshot
Residual Dipolar Couplings of Freely Rotating Groups in Small Molecules. Stereochemical Assignment and Side-Chain Conformation of 8-Phenylmenthol
inferredcites →https://doi.org/10.1038/srep10511openalex-snapshot
Removal of ecotoxicity of 17α-ethinylestradiol using TAML/peroxide water treatment
inferredcites →https://doi.org/10.1039/c1ob05109aopenalex-snapshot
Unprecedented stereoselective synthesis of cyclopenta[b]benzofuran derivatives and their characterisation assisted by aligned media NMR and 13C chemical shift ab initio predictions
inferredcites →https://doi.org/10.1063/1.3359469openalex-snapshot
Continuous surface charge polarizable continuum models of solvation. I. General formalism
inferredcites →https://doi.org/10.1063/1.478522openalex-snapshot
Toward reliable density functional methods without adjustable parameters: The PBE0 model
inferredcites →https://doi.org/10.1107/s0108767388010128openalex-snapshot
On the orthogonal transformation used for structural comparisons
inferredcites →https://doi.org/10.1289/ehp.8050openalex-snapshot
Predicted Exposures to Steroid Estrogens in U.K. Rivers Correlate with Widespread Sexual Disruption in Wild Fish Populations
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/cmtd.202400039openalex-snapshot
Graphene Oxide‐Cyclopentylamine (GO‐d‐CP) Liquid Crystals as a Novel Alignment Medium for Anisotropic NMR with Analyte Recovery
inferred← citeshttps://doi.org/10.1002/mrc.4784openalex-snapshot
Homonuclear decoupling by projection reconstruction
inferred← citeshttps://doi.org/10.1002/mrc.5003openalex-snapshot
Valine derived poly (acetylenes) as versatile chiral lyotropic liquid crystalline alignment media for RDC‐based structure elucidations
inferred← citeshttps://doi.org/10.1002/mrc.5143openalex-snapshot
Practical considerations for working with graphene oxide as alignment media for RDC measurements
inferred← citeshttps://doi.org/10.1016/j.matlet.2024.136526openalex-snapshot
Synthesis and characterization of grafted graphene oxide materials with lyotropic liquid crystalline properties detected by NMR spectroscopy
inferred← citeshttps://doi.org/10.1016/j.pnmrs.2019.10.001openalex-snapshot
Multinuclear NMR in polypeptide liquid crystals: Three fertile decades of methodological developments and analytical challenges
inferred← citeshttps://doi.org/10.1021/accountsmr.3c00181openalex-snapshot
Weak Alignment Liquid Crystal Media from Colloidal Dispersion and Self-assembled Oligopeptide for Anisotropic NMR
inferred← citeshttps://doi.org/10.1038/s41596-018-0091-9openalex-snapshot
Application of anisotropic NMR parameters to the confirmation of molecular structure
inferred← citeshttps://doi.org/10.1039/bk9781839167898-00252openalex-snapshot
Structure Determination of Organic Molecules Using RDCs (and RCSAs)
inferred← citeshttps://doi.org/10.1039/d5qm00847fopenalex-snapshot
Nonpolar graphene oxide (GO-NP): a heterogeneous liquid crystalline alignment medium for anisotropic NMR in nonpolar organic solvents
inferred← citeshttps://doi.org/10.1360/n032017-00124openalex-snapshot
Structural elucidation of organic molecule from residual dipolar couplings
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