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Nuclear magnetic resonance spectroscopy. Carbon-13 chemical shifts in norbornyl derivatives

https://doi.org/10.1021/ja00727a016
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Polycycloalkanes at the Helm: Exploring Efuel with Norbornyl Derivatives
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Fluorination by Sulfur Tetrafluoride
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Downfield chemical shifts at ?-protons and carbons of ?-propiothiolactones
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Stereochemical Aspects of13C NMR Spectroscopy
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Substituent Effects on 13 C Chemical Shifts in Aliphatic Molecular Systems. Dependence on Constitution and Stereochemistry
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Impuls‐Fourier‐Transform‐13C‐NMR‐Spektroskopie, Grundlagen und Anwendungen
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Konformationsuntersuchungen mit der 13C‐Tieftemperatur‐Kernresonanzspektroskopie
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Methylen-norbornadien, ein Bicycloheptafulven
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Pulse Fourier Transform 13C‐NMR Spectroscopy, Principles and Applications
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Conformational Studies by Low Temperature 13C‐NMR Spectroscopy
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Methylenenorbornadiene, a Bicycloheptafulvene
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Insertion and cooxidation of nickel‐bonded methallyl and norbornene ligands
inferred← citeshttps://doi.org/10.1002/bscb.19830920209openalex-snapshot
Acétonylation Radicalaire de la Norbornanone‐2 Par Réaction Avec le Percarbonate de O,O‐t‐Butyle et O‐Isopropenyle
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13C‐ and 1H‐NMR Shielding Effects in Aliphatic gauche/trans Fragments
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ChemInform Abstract: NMR‐SPEKTROSKOPIE, (13)C‐CHEMISCHE VERSCHIEBUNGEN BEI NORBORNYL‐DERIVATEN (INTERPRETATION DURCH INDUKTIVE, STERISCHE UND BINDUNGSLAENGENEFFEKTE, KORRELATION BERECHNETER SUBSTITUENTENVERSCHIEBUNGEN MIT EXPERIMENTELLEN DATEN)
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ChemInform Abstract: ADDITION VON ORGANOMAGNESIUM‐VERBINDUNGEN AN NICHT AKTIVIERTE C=C‐DOPPELBINDUNGEN 4. MITT. BENZYLMAGNESIUMCHLORID UND OLEFINE
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[4+2]‐Cycloadditionen von 1,2‐Dicyanocyclobuten und seine thermische Ringöffnung zum 2,3‐Dicyanobutadien‐1,3
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Secondary 2‐Norbornyl Cation Intermediates Substituted at C(5) and C(7) by Electron‐withdrawing Groups. Addition of fluorosulfuric acid to unsaturated norbornane derivatives
inferred← citeshttps://doi.org/10.1002/hlca.19800630508openalex-snapshot
The Photochemistry of 5,6‐Dimethylidene‐2‐norborananone. Synthesis and Diels‐Alder Reactivity of 2,3‐Dimethylidenebicyclo‐[2.1.1]hexane
inferred← citeshttps://doi.org/10.1002/hlca.19810640613openalex-snapshot
The π‐Anisotropy of the Double Bond of a syn‐11‐Oxasesquinorbornene Derivative.. Stereoselectivity of the Diels–Alder additions of (2‐norborneno)[c]furan. Crystal structure of 11‐oxa‐endo‐tetracyclo[6.2.1.13,6.02,7]‐dodec‐2(7)‐ene‐9,10‐exo‐dicarboxylic anhydride
inferred← citeshttps://doi.org/10.1002/hlca.19830660126openalex-snapshot
Photochemisch induzierte Reaktionen von 3‐Amino‐2H‐azirinen
inferred← citeshttps://doi.org/10.1002/hlca.19970800105openalex-snapshot
Long‐Distance Effect on One‐Bond CC Scalar couplings upon introduction of a double bond in bicyclic systems
inferred← citeshttps://doi.org/10.1002/ijch.198100043openalex-snapshot
Strained Mono‐ and Dications. On the Structures of [(CCH2)7H]2⊕ and [(CCH3)7CH3]2⊕ Dications
inferred← citeshttps://doi.org/10.1002/jhet.5570190542openalex-snapshot
Preparation of new 1,2,4‐triazines
inferred← citeshttps://doi.org/10.1002/jlac.197519750207openalex-snapshot
Naturstoffe aus Arzneipflanzen, XIX1) Zur Konstitutionsermittlung der C15‐Iridoidglucoside und ihrer natürlichen Derivate mit Hilfe der 13C‐NMR‐Spektroskopie
inferred← citeshttps://doi.org/10.1002/jlac.197519750727openalex-snapshot
13C‐NMR‐Spektren epimerer N‐Alkylnoratropinderivate
inferred← citeshttps://doi.org/10.1002/jlac.197519751202openalex-snapshot
Photoelektronenspektren organischer Verbindungen IX. Sterisch fixierte Bicyclopropyle
inferred← citeshttps://doi.org/10.1002/jlac.197719770418openalex-snapshot
Cyclisch gekreuzt‐konjugierte Bindungssysteme, 30. 13C‐Analysen von Methylennorbornadienderivaten
inferred← citeshttps://doi.org/10.1002/jlac.198219820116openalex-snapshot
Synthese von Prostaglandin‐Analoga
inferred← citeshttps://doi.org/10.1002/jlac.198519850718openalex-snapshot
Hydrogenolyse kleiner Kohlenstoffringe, X. über die katalytische Hydrierung der Bicyclo[n.1.0]alkane
inferred← citeshttps://doi.org/10.1002/jps.2600700118openalex-snapshot
PMR and 13C-NMR Spectroscopy of Tropane and N-Substituted Nortropane Spirohydantoins
inferred← citeshttps://doi.org/10.1002/jps.2600750620openalex-snapshot
Microbial Metabolism of Bornaprine, 3-(Diethylamino)propyl 2-Phenylbicyclo[2.2.1]heptane-2-carboxylate
inferred← citeshttps://doi.org/10.1002/macp.200900576openalex-snapshot
Hydroxyl‐Functionalized Norbornene Based Co‐ and Terpolymers by Scandium Half‐Sandwich Catalyst
inferred← citeshttps://doi.org/10.1002/mrc.1260230916openalex-snapshot
Studies in the synthesis of C‐ring bridged morphinans 3—13C NMR analysis of some simple and complex bicyclooctane derivatives
inferred← citeshttps://doi.org/10.1002/mrc.1260231007openalex-snapshot
13C nuclear magnetic resonance spectra of bridged‐ring steroids and related compounds
inferred← citeshttps://doi.org/10.1002/mrc.1260240413openalex-snapshot
Three‐bond carbon–fluorine coupling constants in substituted 3‐fluoropropanes and 3‐fluoropropanoates
inferred← citeshttps://doi.org/10.1002/mrc.1260240512openalex-snapshot
Substituent chemical shifts in NMR. 3—Carbonitrile SCS in rigid molecules
inferred← citeshttps://doi.org/10.1002/mrc.1260260511openalex-snapshot
Deuterium‐induced NMR isotope shifts for 13C resonance frequencies of norbornane. Quantitative data for the dihedral angle dependence of vicinal shifts
inferred← citeshttps://doi.org/10.1002/mrc.1260261111openalex-snapshot
Computer predictions of 13C spectra. II—Alcohols and ketones
inferred← citeshttps://doi.org/10.1002/mrc.1260270314openalex-snapshot
Principal component analysis of the 13C NMR shifts of norbornyl derivatives
inferred← citeshttps://doi.org/10.1002/mrc.1260271111openalex-snapshot
Substituent chemical shifts in NMR. Part 4—1H SCS in some 2‐substituted norbornanes and bornanes
inferred← citeshttps://doi.org/10.1002/mrc.1260280513openalex-snapshot
13C, 1H spin–spin coupling. X—Norbornane: A reinvestigation of the karplus curve for 3J(13C, 1H)
inferred← citeshttps://doi.org/10.1002/mrc.1260280604openalex-snapshot
1H and 13C NMR determination of the relative stereochemistry of the diastereomers resulting from the reaction of sily enol ethers with the 1‐ethoxy‐1‐propargylium dicobalt hexacarbonyl cation
inferred← citeshttps://doi.org/10.1002/mrc.1260280712openalex-snapshot
Structural analysis and complete assignment of the 1H and 13C NMR spectra of thiele's ester
inferred← citeshttps://doi.org/10.1002/mrc.1260281007openalex-snapshot
Carbon‐13 and proton spectra of tetracyclododecanes: Long‐range steric effects
inferred← citeshttps://doi.org/10.1002/mrc.1260300110openalex-snapshot
13C NMR substituent effects in aliphatic systems: Principal component analysis and correlations with electronegativities
inferred← citeshttps://doi.org/10.1002/mrc.1260300903openalex-snapshot
Structural elucidation of disubstituted nortricyclenes through vicinal 13C, 1H coupling constants
inferred← citeshttps://doi.org/10.1002/mrc.1260310306openalex-snapshot
Carbon‐13 NMR spectra of tetracyclododecanes: Evidence for upfield δ and ε steric effects
inferred← citeshttps://doi.org/10.1002/mrc.1270040106openalex-snapshot
13C NMR spectra of cyclopropane derivatives. Stereoisomeric substituted 2‐phenylcyclopropanes
inferred← citeshttps://doi.org/10.1002/mrc.1270050309openalex-snapshot
Configurations and conformations in acyclic, unsaturated hydrocarbons. A 13C NMR study
inferred← citeshttps://doi.org/10.1002/mrc.1270050607openalex-snapshot
Carbon‐13 chemical shifts of substituted nortricyclenes
inferred← citeshttps://doi.org/10.1002/mrc.1270050710openalex-snapshot
Relation between the carbon chemical shifts and the J(CH) spin‐spin coupling constants
inferred← citeshttps://doi.org/10.1002/mrc.1270051006openalex-snapshot
Tris‐(4,4,4‐trifluoro‐1‐(‐2‐thienyl)‐1,3‐butandiono)‐europium(III) als NMR‐Verschiebungsreagens
inferred← citeshttps://doi.org/10.1002/mrc.1270060310openalex-snapshot
13C chemical shifts of monosubstituted adamantanes
inferred← citeshttps://doi.org/10.1002/mrc.1270060312openalex-snapshot
The NMR spectra and conformations of cyclic compounds: IX—conformational studies of bicyclo(3,1,0)hexane derivatives by 13C NMR
inferred← citeshttps://doi.org/10.1002/mrc.1270060610openalex-snapshot
Carbon‐13 magnetic resonance study of spiro compounds
inferred← citeshttps://doi.org/10.1002/mrc.1270060815openalex-snapshot
13C FT‐NMR spectra of alkyl substituted furans. A study of the influence of steric interactions
inferred← citeshttps://doi.org/10.1002/mrc.1270060908openalex-snapshot
Etude par RMN 13C de quelques époxydes exo et endo dans la série du bicyclo[2.2.1]heptane
inferred← citeshttps://doi.org/10.1002/mrc.1270070103openalex-snapshot
Theoretical and empirical calculations of the carbon chemical shift in terms of the electronic distribution in molecules
inferred← citeshttps://doi.org/10.1002/mrc.1270070402openalex-snapshot
Carbon‐13 nuclear magnetic resonance spectra. I—Monosubstituted adamantanes and adamantanones
inferred← citeshttps://doi.org/10.1002/mrc.1270070904openalex-snapshot
Carbon‐13 NMR spectroscopy of hop bitter substances
inferred← citeshttps://doi.org/10.1002/mrc.1270071207openalex-snapshot
13C NMR spectroscopy of four tertiary methyl norbornenols and norbornanols
inferred← citeshttps://doi.org/10.1002/mrc.1270080204openalex-snapshot
Carbon‐13 chemical shifts of bicyclo[3.2.1]octane and bicyclo[2.2.1]heptane derivatives
inferred← citeshttps://doi.org/10.1002/mrc.1270080405openalex-snapshot
Etude stereochimique par RMN du 13C des α‐halogenocyclohexanones
inferred← citeshttps://doi.org/10.1002/mrc.1270080507openalex-snapshot
NMR studies of sulphur heterocycles: III—13C spectra of benzo[b]thiophene and the methylbenzo[b]thiophenes
inferred← citeshttps://doi.org/10.1002/mrc.1270080602openalex-snapshot
NMR‐Untersuchungen an Dicyclopentadienderivaten: II.—13C‐NMR: γ‐gauche‐Effekt in Abhängigkeit von der exo/endo‐Isomerie an Dicyclopentadien diolen
inferred← citeshttps://doi.org/10.1002/mrc.1270080909openalex-snapshot
Temperature effects on 13C n.m.r. chemical shifts of normal alkanes and some line r and branched 1‐alkenes
inferred← citeshttps://doi.org/10.1002/mrc.1270090208openalex-snapshot
NMR‐Untersuchungen an Dicyclopentadienderivaten: III—Stereochemische Zuordnung von überbrückten endo‐Dicyclopentadienderivaten und deren Wagner‐Meerwein‐Umlagerungs‐produkten mit Hilfe der NMR‐Spektroskopie
inferred← citeshttps://doi.org/10.1002/mrc.1270090302openalex-snapshot
13C spectra of some vicinal dimethylene derivatives of cyclic hydrocarbons
inferred← citeshttps://doi.org/10.1002/mrc.1270090604openalex-snapshot
NMR‐Untersuchungen an Dicyclopentadienderivaten. IV—1‐Syn/anti‐Epimere von endo‐Dicyclopentadienderivaten
inferred← citeshttps://doi.org/10.1002/mrc.1270090607openalex-snapshot
Carbon‐13 nuclear magnetic resonance spectra of isomeric oxaziridines. Effects of the nitrogen lone pair on carbon‐13 chemical shifts
inferred← citeshttps://doi.org/10.1002/mrc.1270090616openalex-snapshot
Carbon‐13 n.m.r. studies. Part 66—13C spectra of several methyl, hydroxymethyl and carboxylic acid derivatives of bicyclo[2.2.1]heptane and bicyclo[2.2.2]octane
inferred← citeshttps://doi.org/10.1002/mrc.1270090908openalex-snapshot
Carbon‐13 nuclear magnetic resonance spectra: V—substituent interactions at 4‐substituted adamantanones and bicyclo[2.2.2]octanones
inferred← citeshttps://doi.org/10.1002/mrc.1270091102openalex-snapshot
Carbon‐13 n.m.r. spectra of 2,3‐dimethylenebicyclo[2.2.1]heptanes and 2,3‐dimethylene‐7‐oxabicyclo[2.2.1]heptanes
inferred← citeshttps://doi.org/10.1002/mrc.1270110115openalex-snapshot
A Karplus‐type relationship for the vicinal coupling 3J(CCCP) in phosphonates
inferred← citeshttps://doi.org/10.1002/mrc.1270110203openalex-snapshot
Proximity and the heteroatom effects on the carbon‐13 chemical shifts of methyl‐substituted phenols, anilines and thiophenols
inferred← citeshttps://doi.org/10.1002/mrc.1270110205openalex-snapshot
Carbon‐13 NMR studies. 73—carbon‐13 spectra of several 10‐methyl‐trans‐decalins. Further definition of the deshielding antiperiplanar γ effect
inferred← citeshttps://doi.org/10.1002/mrc.1270110207openalex-snapshot
RMN 13C d'Alcynes Aliphatiques: Analyse Topologique des Effets de Substituants Alkyles sur les Déplacements Chimiques des Carbones sp par la Méthode DARC PELCO
inferred← citeshttps://doi.org/10.1002/mrc.1270110710openalex-snapshot
A carbon‐13 NMR study of benzonorbornene isomers
inferred← citeshttps://doi.org/10.1002/mrc.1270111008openalex-snapshot
15N nuclear magnetic resonance spectroscopy. Natural‐abundance 15N spectra of aliphatic oximes
inferred← citeshttps://doi.org/10.1002/mrc.1270111010openalex-snapshot
Cage compounds IV. 1H and 13C NMR study of 3,6‐epoxypentacyclo‐[6.2.2.02,7.04,10.05,9]dodecane and 3,6‐epoxypentacyclo‐[6.2.1.02,7.04,10.05,9]undecane
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.1270120302openalex-snapshot
13C NMR of polycyclic aromatic compounds. A review
inferred← citeshttps://doi.org/10.1002/mrc.1270120405openalex-snapshot
Comparison of steric effects on 31P chemical shifts in some 7‐norbornyl, 7‐norbornenyl and cyclohexyl phosphorus compounds
inferred← citeshttps://doi.org/10.1002/mrc.1270120609openalex-snapshot
Carbon‐13 magnetic resonance: γ‐anti substituent effects
inferred← citeshttps://doi.org/10.1002/mrc.1270120708openalex-snapshot
13C NMR spectroscopy of natural substances: IV—13C NMR studies of trachylobane diterpenes: Complete carbon assignment
inferred← citeshttps://doi.org/10.1002/mrc.1270121108openalex-snapshot
13C‐NMR‐spektroskopische und stereochemische Untersuchungen. XXIII.—Konformationen, 13C‐NMR‐Verschiebungen‐ und 13C1H‐ Kopplungen bei Pinanverbindungen
inferred← citeshttps://doi.org/10.1002/mrc.1270140423openalex-snapshot
13C NMR Spectra of some diterpenes of Premna latifolia Roxb
inferred← citeshttps://doi.org/10.1002/mrc.1270140516openalex-snapshot
A carbon‐13 nuclear magnetic resonance study of compounds substituted by a perfluoroalkyl chain
inferred← citeshttps://doi.org/10.1002/mrc.1270150103openalex-snapshot
Nitrogen‐15 nuclear magnetic resonance spectroscopy. Natural abundance nitrogen‐15 spectra of the cis and trans isomers of secondary alkylformamides
inferred← citeshttps://doi.org/10.1002/mrc.1270170105openalex-snapshot
13C NMR spectral studies of zoapatanol and montanol, novel diterpenes from Montanoa tomentosa (zoapatle), and their chemical derivatives
inferred← citeshttps://doi.org/10.1002/mrc.1270170211openalex-snapshot
Carbon‐13 nuclear magnetic resonance studies of thiocarbamates, S‐oxides and S,S‐dioxides
inferred← citeshttps://doi.org/10.1002/mrc.1270170409openalex-snapshot
Dependence of the γ carbon‐13 shielding effect on the dihedral angle
inferred← citeshttps://doi.org/10.1002/mrc.1270200112openalex-snapshot
1H and 13C NMR spectral studies of C‐2 substituted isomeric exo‐ and endo‐5‐methyl‐bicyclo[3.2.1]octane‐6,8‐diones
inferred← citeshttps://doi.org/10.1002/mrc.1270200205openalex-snapshot
13C NMR spectra of phosphole–P(IV) dimers; ABX and AA′X 13C31P coupling in some derived structures
inferred← citeshttps://doi.org/10.1002/mrc.1270200318openalex-snapshot
Substituent parameters v. Lanthanide‐induced shifts in the interpretation of the 13C nuclear magnetic resonance spectrum of 5,5‐dimethyl‐2‐norbornanone
inferred← citeshttps://doi.org/10.1002/mrc.1270200402openalex-snapshot
13C NMR of camphene and α‐pinene: Revised assignments
inferred← citeshttps://doi.org/10.1002/mrc.1270220213openalex-snapshot
Pairwise effects of chlorine substituents on the 13C NMR chemical shifts of dichlorobicyclo[2.2.1]heptanes (norbornanes)
inferred← citeshttps://doi.org/10.1002/mrc.1270220602openalex-snapshot
Application of NMR spectroscopy of chiral association complexes. 14—chiral recognition of terpene and cyclohexene hydrocarbons by 1H and 13C NMR
inferred← citeshttps://doi.org/10.1002/mrc.1483openalex-snapshot
Non‐empirical calculations of NMR indirect carbon–carbon coupling constants. Part 10—Carbocages
inferred← citeshttps://doi.org/10.1002/mrc.1515openalex-snapshot
Non‐empirical calculations of NMR indirect carbon–carbon coupling constants. Part 11—saturated carbocycles: a reference data set and a practical guide to structural elucidation
inferred← citeshttps://doi.org/10.1002/omr.1270210215openalex-snapshot
13C NMR shifts and conformations of substituted indans
inferred← citeshttps://doi.org/10.1002/omr.1270210806openalex-snapshot
Carbon‐13 magnetic resonance spectra and the stereochemistry of some substituted bicyclo[2.1.1]hexanes
inferred← citeshttps://doi.org/10.1002/prac.19823240416openalex-snapshot
NMR‐Untersuchungen an Dicyclopentadien‐Derivaten. VII. Zur Abhängigkeit des γ‐gauche Effektes von der sterischen Kompression eng benachbarter Protonen bei exo/endo‐Isomerieumkehr
inferred← citeshttps://doi.org/10.1002/prac.19903320412openalex-snapshot
Zur näheren Kenntnis des 1‐Camphenylsystems ‐ 1‐Camphenylverbindungen des Lithiums, Zinns und Quecksilbers
inferred← citeshttps://doi.org/10.1002/prac.19963380154openalex-snapshot
Synthesis of Fluoromonoterpenoids as potential suicide substrates for plant cells
inferred← citeshttps://doi.org/10.1002/recl.19750940810openalex-snapshot
A 13C‐NMR study of squalene some aspects of the selective terminal oxidation of squalene
inferred← citeshttps://doi.org/10.1002/recl.19780970502openalex-snapshot
Préparation et propriétés de cyclobutanethiones
inferred← citeshttps://doi.org/10.1002/recl.19811000303openalex-snapshot
An additivity relation for carbon‐13 chemical shifts in substituted allenes
inferred← citeshttps://doi.org/10.1002/recl.19831020208openalex-snapshot
Photochemical reactions of 2‐bornanethione (thiocamphor) with bis(methylthio)ethyne. Addition and intramolecular hydrogen abstraction
inferred← citeshttps://doi.org/10.1002/zaac.19814831218openalex-snapshot
Koordinationschemische Untersuchungen an Zinkdialkylen. XVI. Darstellung und Untersuchung von Dinorbornylzink‐Verbindungen
inferred← citeshttps://doi.org/10.1002/zaac.19824940118openalex-snapshot
Koordinationschemische Untersuchungen an Zinkdialkylen. XVII [1]. Bis(3‐nortricyclyl)zink und dessen komplexchemisches Verhalten
inferred← citeshttps://doi.org/10.1007/978-1-4615-8660-9_4openalex-snapshot
Linear Correlations of Substituent Effects in 1H, 19F, and 13C Nuclear Magnetic Resonance Spectroscopy
inferred← citeshttps://doi.org/10.1007/978-94-009-3161-9_6openalex-snapshot
Bicyclo[2.2.1]heptanes
inferred← citeshttps://doi.org/10.1007/bf00475392openalex-snapshot
Research on 1-aza two-ring systems
inferred← citeshttps://doi.org/10.1007/bf00566076openalex-snapshot
13C NMR spectra of handelin and its derivatives
inferred← citeshttps://doi.org/10.1007/bf00704004openalex-snapshot
Reactions of heptacyclo[8.4.0.02,12.03,8.04,6.05,9.011,13]tetradecane (binor-s) with acids and alcohols catalyzed by Pd, Rh, and Pt complexes and some transformations of the compounds formed
inferred← citeshttps://doi.org/10.1007/bf00808747openalex-snapshot
Stereochemical dependence of13C-shift and31P-13C-coupling in 3-substituted bicyclo[2.2.1]hept-5-en-2-yl- and bicyclo[2.2.2]oct-5-en-2-yl-phosphonates
inferred← citeshttps://doi.org/10.1007/bf00924563openalex-snapshot
An unusual rearrangement and addition of solvent during the photolysis of alkyl-substituted bicyclo[3.2.0 ]hept-6-en-2-ones in methanol
inferred← citeshttps://doi.org/10.1007/bf00949621openalex-snapshot
13C NMR spectra of stereoisomeric derivatives of bicyclo[2.2.1]-hept-5-ene and 3-oxatricyclo[3.2.1.02,4]octane
inferred← citeshttps://doi.org/10.1007/bf00951876openalex-snapshot
Investigation of substituted bicyclo[4.2.0]oct-7-en-2-ones by13C NMR spectroscopy
inferred← citeshttps://doi.org/10.1007/bf00957314openalex-snapshot
Synthesis, stereochemistry, and13C and1H NMR spectra of adducts of acrylic dienophiles with 5-ethoxy-2-carbethoxy-4-carbethoxymethyloxazole
inferred← citeshttps://doi.org/10.1007/bf01108217openalex-snapshot
13C NMR spectra of exo, exo- and exo,endo-stereoisomers of tetracyclo[6.2.1.02,7.13,6]dodecane
inferred← citeshttps://doi.org/10.1007/bf01120978openalex-snapshot
Diisophorone and related compounds. Part 1413C-nuclear magnetic resonance spectra of diisophorone carboxylic acids
inferred← citeshttps://doi.org/10.1007/bf02856301openalex-snapshot
Carbon-13 NMR spectra of phytolaccagenin and its glycosides
inferred← citeshttps://doi.org/10.1007/s10593-013-1206-4openalex-snapshot
Stereoselective synthesis of 1-methyl-1,2-and 1,3-cyclopentanediols via γ-lactones
inferred← citeshttps://doi.org/10.1016/0009-2614(90)85539-oopenalex-snapshot
Ab initio charge distribution in tetracyclic norbornyl derivatives
inferred← citeshttps://doi.org/10.1016/0022-2364(77)90014-2openalex-snapshot
Carbon-13 spectra of some insect pheromones and related compounds of the 6-8-dioxabicyclo (3.2.1)octane system
inferred← citeshttps://doi.org/10.1016/0022-2364(77)90023-3openalex-snapshot
Analysis of 13C NMR data by means of pattern recognition methodology
inferred← citeshttps://doi.org/10.1016/0022-2364(79)90243-9openalex-snapshot
Carbon-13 NMR studies of camphene in the plastic crystalline phase
inferred← citeshttps://doi.org/10.1016/0022-2364(80)90173-0openalex-snapshot
Internal rotation of methyl groups in terpenes. Variable-temperature carbon-13 spin-lattice relaxation time measurements and force-field calculations
inferred← citeshttps://doi.org/10.1016/0022-2852(72)90027-6openalex-snapshot
Long-range carbon-carbon spin-spin coupling constants from 1-13C-labeled toluene
inferred← citeshttps://doi.org/10.1016/0022-2860(74)87003-1openalex-snapshot
Structure électronique de systèmes contraints. Effet reflexe. I. Hydrocarbures
inferred← citeshttps://doi.org/10.1016/0022-2860(81)85238-6openalex-snapshot
Structural study of tropane-3-spiro-4'-imidazol-5'-one
inferred← citeshttps://doi.org/10.1016/0022-2860(88)85030-0openalex-snapshot
Intramolecular non-bonded interactions and β- and γ-hydroxy substituent 13C NMR chemical shifts
inferred← citeshttps://doi.org/10.1016/0022-328x(88)83064-xopenalex-snapshot
Chemie der Isoblausäure V. Reaktionen von W(CO)5CNH, Fe(CN)2(CNH)4 und [FeCp(dppe)CNH]BF4 mit hochalkylierten Olefinen: hydroisocyanierung
inferred← citeshttps://doi.org/10.1016/0022-328x(91)86174-oopenalex-snapshot
Preparation, structure, and reaction of the tricarbonyliron complex of tricyclo[5.3.1.04,9]undeca-2,5-diene, a strongly homo-conjugated nonparallel 1,4-diene
inferred← citeshttps://doi.org/10.1016/0031-9422(92)80460-vopenalex-snapshot
Cryptoquinonemethides D and E, C30-terpene quinone methides, from Cryptomeria japonica
inferred← citeshttps://doi.org/10.1016/0039-128x(82)90061-7openalex-snapshot
5α,6α- AND 5β,6β-dichloromethylene adducts of 3β-acetoxy-5-androsten-17-one
inferred← citeshttps://doi.org/10.1016/0040-4020(75)80207-9openalex-snapshot
Lanthanide induced 1H and 13C NMR shifts and their use for geometry analysis with alicyclic compounds
inferred← citeshttps://doi.org/10.1016/0040-4020(75)85096-4openalex-snapshot
An INDO-LMO and 13C NMR spectroscopic study of the C-H bonds in tetracyclo[3.2.0.02,7.04,6]heptane (quadricyclane) and tricyclo[3.1.0.02,4]hexane
inferred← citeshttps://doi.org/10.1016/0040-4020(75)87014-1openalex-snapshot
13C Nuclear magnetic resonance spectra of 2-substituted bicyclo(3.3.1)nonan-9-ones
inferred← citeshttps://doi.org/10.1016/0040-4020(77)80138-5openalex-snapshot
13C-NMR-Spektroskopische und stereochemische untersuchungen—XIV
inferred← citeshttps://doi.org/10.1016/0040-4020(77)80386-4openalex-snapshot
13C nuclear magnetic resonance spectra—VI
inferred← citeshttps://doi.org/10.1016/0040-4020(77)80389-xopenalex-snapshot
13C NMR substituent effects in tetracyclic diterpenoids
inferred← citeshttps://doi.org/10.1016/0040-4020(77)84058-1openalex-snapshot
13C-19F couplings and 19F NMR shifts of cycloalkyl, bicycloalkyl and steroid monofluoro compounds
inferred← citeshttps://doi.org/10.1016/0040-4020(78)80116-1openalex-snapshot
13C NMR Chemical shifts in bicyclo[2.2.2]octanes—iii
inferred← citeshttps://doi.org/10.1016/0040-4020(78)88047-8openalex-snapshot
Configurational assignment by NMR spectroscopy of stereoisomeric 2,6-dimethyl-tricyclo[5.2.1.02,6]dec-3-enes and decanes
inferred← citeshttps://doi.org/10.1016/0040-4020(78)88334-3openalex-snapshot
Factors affecting the endo : exo ratio in diels-alder reactions of cyclopentadiene
inferred← citeshttps://doi.org/10.1016/0040-4020(80)80029-9openalex-snapshot
Some regioselective reactions of photoaldrin and photodieldrin
inferred← citeshttps://doi.org/10.1016/0040-4020(80)80156-6openalex-snapshot
Oxygen-17 nuclear magnetic resonance
inferred← citeshttps://doi.org/10.1016/0040-4039(93)85007-jopenalex-snapshot
The Gamma Gauche Substituent Effect in 13C NMR1
inferred← citeshttps://doi.org/10.1016/0079-6565(79)80006-0openalex-snapshot
Carbon-carbon coupling constants: A compilation of data and a practical guide
inferred← citeshttps://doi.org/10.1016/0079-6565(89)80007-xopenalex-snapshot
Structural applications of one-bond carboncarbon spin—spin coupling constants
inferred← citeshttps://doi.org/10.1016/0079-6565(91)80004-lopenalex-snapshot
Spin—spin coupling constants between carbons separated by more than one bond
inferred← citeshttps://doi.org/10.1016/0166-1280(86)80093-8openalex-snapshot
13C chemical shifts in series of adamantane and norbornane derivatives. INDO calculations
inferred← citeshttps://doi.org/10.1016/0166-1280(88)80016-2openalex-snapshot
Intramolecular non-bonded interactions and β- and γ-substituent 13C NMR chemical shifts: application to series of adamantane and norbornane derivatives
inferred← citeshttps://doi.org/10.1016/0584-8539(87)80124-1openalex-snapshot
Correlations of chemical shifts of saturated carbon atoms that have a directly bonded substituent
inferred← citeshttps://doi.org/10.1016/b978-0-12-784309-4.50007-8openalex-snapshot
Nuclear Magnetic Resonance Spectroscopy
inferred← citeshttps://doi.org/10.1016/j.cplett.2011.05.015openalex-snapshot
Computational and experimental studies into NMR characterization of [2+2] cycloaddition products of norbornene
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.02.013openalex-snapshot
Activation of the Ge–H bond of Et3GeH in photochemical reaction with molybdenum(0) carbonyl complexes and hydrogermylation of norbornadiene
inferred← citeshttps://doi.org/10.1016/j.molcata.2008.02.005openalex-snapshot
Facile hydrosilylation of norbornadiene by silanes R3SiH and R2SiH2 with molybdenum catalysts
inferred← citeshttps://doi.org/10.1016/j.mtchem.2024.102264openalex-snapshot
Polycycloalkanes at the Helm: Exploring high energy density eFuel with norbornyl derivatives
inferred← citeshttps://doi.org/10.1016/j.polymer.2004.01.056openalex-snapshot
Forgotten monomers: free radical polymerization behavior of norbornadiene derivatives in comparison with methyl methacrylate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.01.031openalex-snapshot
W(II)-catalyzed hydroarylation of bicyclo[2.2.1]hept-2-ene by simple arenes
inferred← citeshttps://doi.org/10.1016/s0003-2670(00)83628-4openalex-snapshot
Feature extraction from spectral and other data by the principal components and discriminant function techniques
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)80659-2openalex-snapshot
Transition metal promoted reactions of unsaturated hydrocarbons
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)80661-0openalex-snapshot
A 13C and 1H NMR investigation of the bonding in norbornenyl complexes of palladium(II) and platinum(II)
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)81537-5openalex-snapshot
Hydrosilylation of bicyclo[2.2.1]heptene derivatives by trichlorosilane with the use of Ni catalytic systems A study of the stereochemistry of the process
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)85072-xopenalex-snapshot
Synthesis and spectroscopic studies of some novel bicyclic organotin compounds
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)85640-5openalex-snapshot
Electrophilically-induced cyclodestannylation reactions
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)86765-0openalex-snapshot
Nickel(0)-induzierte c—c-verknüpfung zwischen alkenen und kohlendioxid
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)88665-9openalex-snapshot
Addition von organomagnesium-verbindungen an nicht aktivierte CC-doppelbindungen. II
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)89751-xopenalex-snapshot
Transition metal-promoted reactions of unsaturated hydrocarbons
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)91376-7openalex-snapshot
Tin-119 magnetic shielding in norbornenyltrimethyltins
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)99510-xopenalex-snapshot
Preparation and reactions of hydroxo-enylpalladium(II) derivatives
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)85976-7openalex-snapshot
Novel products from Beckmann fragmentation of camphor oxime in polyphosphoric acid
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)85985-8openalex-snapshot
New processes for the halofluorination of norbornadiene. Structural reexamination of the products. Evidence for exclusive exo attack by electrophiles
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)89045-1openalex-snapshot
15N nuclear magnetic resonance studies of azabicycles; unusual deshielding of nitrogen in the 7-azabicyclo[2.2.1]heptyl ring system
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)90900-7openalex-snapshot
Cyclization and rearrangements of diterpenoids—I
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)91505-4openalex-snapshot
Deplacements homolytiques intramoleculaires-I
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)92038-1openalex-snapshot
Carbonyl carbon chemical shifts in the 13c spectra of cyclic ketones
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)93515-xopenalex-snapshot
NMR and stereochemical studies of non aromatic heterocyclic compounds—II
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)93698-1openalex-snapshot
Substituent effects in 13C NMR spectra of 6-endo substituted 9-thiabicyclo[3.3.1]non-2-enes
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)96404-xopenalex-snapshot
Dienophilie des cyano-1 enamines, nouveaux equivalents de cetenes pour les cycloadditions de diels-alder
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)01091-3openalex-snapshot
Stereocontrol in hydride addition to ketone-derived chiral N-acylhydrazones
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00194-5openalex-snapshot
Synthesis of the C17–C23 subunit of Ionomycin from C1-functionalized 8-oxabicyclo[3.2.1]oct-6-en-3-one. New synthetic methodology to prepare polyfunctionalized heptane building blocks with four stereocenters
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)71273-1openalex-snapshot
Strained ring systems. XV. A regiospecific, nonconcerted semi-benzilic acid rearrangement of -2-methoxy-1,4-dichlorobicyclo[2.2.1]heptan-7-one
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)71858-2openalex-snapshot
Regiospecific addition of TCNE to 2--methyl--tricyclo [3.2.1.02,4] oct-6-ene
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)78640-0openalex-snapshot
Effet-methyle en α d'un site 13C - inversion et prevision
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)85285-5openalex-snapshot
One-methylene incorporated dimerization reaction of ketone enolates. 1. A new route to 1,5-diketones from ketones having α-active hydrogen on one side
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)92963-0openalex-snapshot
Carbon-13 NMR spectrum of a new hydrocarbon containing carbon atoms with “inverted” tetrahedral geometry
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)80899-6openalex-snapshot
Asymmetric diels-alder reaction between the chiral isoprene units 2-(r)-and (s)-benzyloxy-2,5-dihydro-4-furancarboxaldehyde and cyclopentadiene
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)81947-xopenalex-snapshot
Correlation des effets (α-Me) en RMN13C: modele topologique par difference lineaire DARC-PULFO.
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)82206-1openalex-snapshot
NMR studies of bridged ring systems. XVIII. Remarkable steric γ effect upon 13C chemical shifts in tricyclo[3.2.1.O2,4]octenes and its application to 13C signal assignment of 9-isopropylidenebenzonorbornene derivatives
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)82275-9openalex-snapshot
Equilibria and 13CMR shifts of cyclohexane conformers
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)86431-5openalex-snapshot
Synthesis of Bicyclo[2.2.1]heptan-2-ones by thermal cyclization of 3-allylcyclopentanones
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)86962-8openalex-snapshot
Carbon-13 nuclear magnetic resonance spectroscopy of C/D- polyoxypregnanes. II
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)87600-0openalex-snapshot
Arynic condensation of ketone enolates. VIII One step synthesis of dibenzotricyclo [4,2,2,12,5] undeca-8,10-diene-1-ol structure elucidation by 13C and 1H NMR
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)91425-xopenalex-snapshot
Long range 13C19F and 1H19F coupling in fluorosteroids
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