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Nuclear magnetic resonance spectroscopy. Carbon-13 chemical shifts of chlorinated organic compounds

https://doi.org/10.1021/jo00923a026
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2,3,4,5,6,6-Hexachloro-2,4-cyclohexadien-1-one
inferred← citeshttps://doi.org/10.1002/1099-0682(200209)2002:9<2271::aid-ejic2271>3.0.co;2-4openalex-snapshot
1,2-Dichalcogenolylium Ions (C3Cl3E3)+ from Equilibria Involving Dichalcogen Dichlorides E2Cl2 (E = S, Se, Te) − Syntheses and Crystal Structures of (C3Cl3S2)Cl, (C3Cl3Se2)Cl, and (C3Cl3Te2)2[Te2Cl10]
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Substituent Effects on 13 C Chemical Shifts in Aliphatic Molecular Systems. Dependence on Constitution and Stereochemistry
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Vortäuschung von CC‐Bindungen durch ungewöhnlich große 2JCC‐Werte – ein Problem bei der Anwendung der INADEQUATE‐13C‐NMR‐Spektroskopie
inferred← citeshttps://doi.org/10.1002/ange.19870990707openalex-snapshot
Bestimmung des Kohlenstoffgerüsts organischer Verbindungen durch Doppelquanten-Kohärenz-13C-NMR-Spektroskopie, die INADEQUATE-Pulsfolge
inferred← citeshttps://doi.org/10.1002/ange.202412745openalex-snapshot
Curvature‐Induced Electron Spin Catalysis with Carbon Spheres
inferred← citeshttps://doi.org/10.1002/anie.198508541openalex-snapshot
Misinterpretation of CC Bonding through Unusually Large 2J CC Values—a Caveat for the Use of INADEQUATE‐13C‐NMR Spectroscopy
inferred← citeshttps://doi.org/10.1002/anie.198706251openalex-snapshot
Direct Identification of the Carbon Skeleton of Organic Compounds using Double Quantum Coherence 13C‐NMR Spectroscopy. The INADEQUATE Pulse Sequence
inferred← citeshttps://doi.org/10.1002/anie.202412745openalex-snapshot
Curvature‐Induced Electron Spin Catalysis with Carbon Spheres
inferred← citeshttps://doi.org/10.1002/cber.19861190611openalex-snapshot
Konstitutionsermittlung hochchlorierter organischer Verbindungen durch INADEQUATE‐13C‐Kernresonanzspektroskopie
inferred← citeshttps://doi.org/10.1002/cber.19911240548openalex-snapshot
Alkine und Cumulene, XXIII. über einige Neben‐ und Folgeprodukte der Dichlorketen‐Herstellung aus α,α‐Dichloracetylchlorid
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Notiz/Note Zur Stereochemie der Reaktion von Vinylhalogeniden mit Perchlorcyclopentadien: Cycloaddition über Vinylkationen
inferred← citeshttps://doi.org/10.1002/chin.197437060openalex-snapshot
ChemInform Abstract: NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, CARBON‐13 CHEMICAL SHIFTS OF CHLORINATED ORGANIC COMPOUNDS
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Thermisch instabile Allene, X. Perchlor‐3,4‐pentadiensäure und Fragmentierung des Dimeren zum Perchlor‐3,4‐bis(methylen)‐1‐vinylcyclobuten
inferred← citeshttps://doi.org/10.1002/jlac.197819781109openalex-snapshot
Allylumlagerung und Ringerweiterung des Perchlor(4‐methylbicyclo[3.2.0]hepta‐2,6‐diens) zum Perchlorbicyclo[3.3.0]‐octa‐2,6‐dien
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Strukturanalyse hochchlorierter Butensäuren durch C‐NMR‐Spektroskopie
inferred← citeshttps://doi.org/10.1002/mrc.1270070802openalex-snapshot
Carbon‐13 NMR spectra of some polychloro hydrocarbons and related compounds
inferred← citeshttps://doi.org/10.1002/mrc.1270071212openalex-snapshot
35Cl/37Cl isotope effects on 13C chemical shifts. Assignment of carbon‐13 NMR lines of polychlorinated hydrocarbons
inferred← citeshttps://doi.org/10.1002/mrc.1270090910openalex-snapshot
Spectroscopic characterization of some chlorinated tricyclic hydrocarbons of the C10 series: Chlordanes, chlordenes and nonachlors
inferred← citeshttps://doi.org/10.1002/mrc.1270111103openalex-snapshot
Carbon‐13 NMR spectra of some chlorinated polycyclodiene pesticides
inferred← citeshttps://doi.org/10.1002/mrc.1270130514openalex-snapshot
Polyhaloheterocyclic compounds. Part XXXI—carbon‐13 NMR spectra as a structural probe for polychloroaromatic compounds
inferred← citeshttps://doi.org/10.1002/mrc.1270150204openalex-snapshot
Carbon‐13 NMR spectra of DDT, its analogues and related compounds
inferred← citeshttps://doi.org/10.1002/mrc.1270160402openalex-snapshot
Carbon‐13 NMR spectra of polybromoalkanes and polychlorobromoalkanes. Structural increments of halogens in polyhalogenated groups
inferred← citeshttps://doi.org/10.1007/978-1-4899-4638-6_1openalex-snapshot
Dictionary of Inorganic Compounds
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_1207openalex-snapshot
Nuclear magnetic resonance data of C7H6Cl4O2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_182openalex-snapshot
Nuclear magnetic resonance data of C3Cl4
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_183openalex-snapshot
Nuclear magnetic resonance data of C3Cl5F3
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_184openalex-snapshot
Nuclear magnetic resonance data of C3Cl6
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_185openalex-snapshot
Nuclear magnetic resonance data of C3Cl6F2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_186openalex-snapshot
Nuclear magnetic resonance data of C3Cl6O
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_188openalex-snapshot
Nuclear magnetic resonance data of C3Cl8
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_385openalex-snapshot
Nuclear magnetic resonance data of C4Cl4F4
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_386openalex-snapshot
Nuclear magnetic resonance data of C4Cl4O
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_387openalex-snapshot
Nuclear magnetic resonance data of C4Cl6
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_388openalex-snapshot
Nuclear magnetic resonance data of C4Cl6
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_389openalex-snapshot
Nuclear magnetic resonance data of C4Cl10
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_60openalex-snapshot
Nuclear magnetic resonance data of C2Cl4
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_61openalex-snapshot
Nuclear magnetic resonance data of C2Cl4F2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_62openalex-snapshot
Nuclear magnetic resonance data of C2Cl6
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_630openalex-snapshot
Nuclear magnetic resonance data of C5Br6
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_631openalex-snapshot
Nuclear magnetic resonance data of C5Cl4O2
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_632openalex-snapshot
Nuclear magnetic resonance data of C5Cl6
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_633openalex-snapshot
Nuclear magnetic resonance data of C5Cl6O
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_634openalex-snapshot
Nuclear magnetic resonance data of C5Cl6O
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_636openalex-snapshot
Nuclear magnetic resonance data of C5H2Cl4
inferred← citeshttps://doi.org/10.1007/978-3-540-45285-0_885openalex-snapshot
Nuclear magnetic resonance data of C6Cl6O
inferred← citeshttps://doi.org/10.1007/bf00948510openalex-snapshot
Radical reactions of perchlorocyclodienes in the presence of coordination initiators based on Fe(CO)5
inferred← citeshttps://doi.org/10.1007/bf00952478openalex-snapshot
Fluoroindenes
inferred← citeshttps://doi.org/10.1007/bf00962460openalex-snapshot
An unusual transformation of perfluorinated 1- and 3-phenylpropenes to polyfluorochloroindanes by the action of AlCl3
inferred← citeshttps://doi.org/10.1007/bfb0048476openalex-snapshot
The development of polyquinane chemistry
inferred← citeshttps://doi.org/10.1007/s10870-017-0694-yopenalex-snapshot
Cl⋯Cl and Cl⋯H Interactions in the Chlorinated Hydocarbon 1,1,1,2,2,3,3-Heptachloropropane: A Structural Study
inferred← citeshttps://doi.org/10.1016/0022-2860(82)85112-0openalex-snapshot
The “cis effect” in β-substituted vinyl ethers and halides
inferred← citeshttps://doi.org/10.1016/0040-4020(76)85216-7openalex-snapshot
NMR-spektroskopische untersuchungen zur kinetik und thermodynamik reversibler dissoziationsreaktionen—II
inferred← citeshttps://doi.org/10.1016/0079-6565(81)80001-5openalex-snapshot
Carbon—hydrogen spin—spin coupling constants
inferred← citeshttps://doi.org/10.1016/0147-6513(92)90051-4openalex-snapshot
Reaction of hexachlorocyclopentadiene with sulfuric acid
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)91162-1openalex-snapshot
The conformational study of the new ergot alkaloids agroclavine-I and epoxyagroclavine-I by proton magnetic resonance spectroscopy
inferred← citeshttps://doi.org/10.1021/ac60369a015openalex-snapshot
Nuclear magnetic resonance spectroscopy
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00188openalex-snapshot
High-Throughput in Silico Structure Validation and Revision of Halogenated Natural Products Is Enabled by Parametric Corrections to DFT-Computed 13 C NMR Chemical Shifts and Spin–Spin Coupling Constants
inferred← citeshttps://doi.org/10.1021/jp066193fopenalex-snapshot
Ultrafast Relaxation Dynamics of Perchlorinated Cycloheptatriene in Solution
inferred← citeshttps://doi.org/10.1080/10408447609164019openalex-snapshot
Chemical Reactivity, Biotransformation, and Toxicity of Polychlorinated Aliphatic Compounds
inferred← citeshttps://doi.org/10.1201/9781420039917.ch9openalex-snapshot
Nuclear Magnetic Resonance Spectroscopy
inferred← citeshttps://doi.org/10.1201/b10385-10openalex-snapshot
Supercritical Fluid Extraction and Chromatography
inferred← citeshttps://doi.org/10.1246/bcsj.48.2464openalex-snapshot
The Carbonyliron Complexes of Some Chlorocarbons
inferred← citeshttps://doi.org/10.1246/bcsj.56.481openalex-snapshot
Synthesis of Octachlorobicyclo[3.3.0]octa-1,4,6-triene and Lewis Acid Catalyzed Isomerization of Hexachlorobicyclo[3.3.0]octa-3,5,8-trien-2-one
inferred← citeshttps://doi.org/10.1246/cl.1977.819openalex-snapshot
STABLE CYCLOPENTADIENONE DERIVATIVES. PERCHLORO-2H,5H-CYCLOPENTA[b]PYRAN-5-ONE AND -2,5-DIONE
inferred← citeshttps://doi.org/10.3390/md22040171openalex-snapshot
Aurantoside L, a New Tetramic Acid Glycoside with Anti-Leishmanial Activity Isolated from the Marine Sponge Siliquariaspongia japonica
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