On the public citation graph
Low temperature 13C NMR magnetic resonance in solids 4. Cyclopropane, bicyclo[1.1.0]butane and [1.1.1] propellane
0 signed · 61 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cber.19751080836openalex-snapshot
13C‐NMR‐Spektren von Bicyclo[n.1.0]kohlenwasserstoffen
inferredcites →https://doi.org/10.1002/ijch.198000020openalex-snapshot
Theory of Magnetic Susceptibilities and NMR Chemical Shifts in Terms of Localized Quantities
inferredcites →https://doi.org/10.1016/0009-2614(75)85672-7openalex-snapshot
Extended basis set studies of hydrocarbon molecular orbital energies
inferredcites →https://doi.org/10.1021/j100243a014openalex-snapshot
Ab initio prediction of structures, force constants and vibrational frequencies. Saturated three-membered rings cyclopropane, ethylene oxide, and ethyleneimine
inferredcites →https://doi.org/10.1021/ja00315a022openalex-snapshot
The carbon 1-carbon 3 bond in [1.1.1]propellane
inferredcites →https://doi.org/10.1021/ja00337a003openalex-snapshot
Low-temperature carbon-13 magnetic resonance in solids. 3. Linear and pseudolinear molecules
inferredcites →https://doi.org/10.1021/ja00339a003openalex-snapshot
Nuclear magnetic shielding in cyclopropane and cyclopropenyl cation
inferredcites →https://doi.org/10.1021/ja00343a025openalex-snapshot
Strain energies of small ring propellanes
inferredcites →https://doi.org/10.1021/ja00343a049openalex-snapshot
Theory of magnetic susceptibilities and NMR chemical shifts in terms of localized quantities. 3. Application to hydrocarbons and other organic molecules
inferredcites →https://doi.org/10.1021/ja00398a053openalex-snapshot
Carbon-13 magnetic resonance dipolar spectroscopy. Orientation of the chemical shift tensor in cyclopropane
inferredcites →https://doi.org/10.1021/ja00401a001openalex-snapshot
Carbon-13 dipolar spectroscopy of small organic molecules in argon matrixes
inferredcites →https://doi.org/10.1021/ja00542a003openalex-snapshot
Low-temperature carbon-13 magnetic resonance of solids. 1. Alkenes and cycloalkenes
inferredcites →https://doi.org/10.1021/ja00758a016openalex-snapshot
Theoretical studies of tricyclo[1.1.1.01,3]pentane and bicyclo[1.1.1]pentane
inferredcites →https://doi.org/10.1021/ja00758a017openalex-snapshot
Electronic structure and reactivity of strained tricyclic hydrocarbons
inferredcites →https://doi.org/10.1063/1.1671318openalex-snapshot
Microwave Spectrum and Structure of Bicyclo[1.1.0]butane
inferredcites →https://doi.org/10.1063/1.439973openalex-snapshot
Orientation of tensorial interactions determined from two-dimensional NMR powder spectra
inferredcites →https://doi.org/10.1063/1.443165openalex-snapshot
Theory of magnetic susceptibilities and NMR chemical shifts in terms of localized quantities. II. Application to some simple molecules
inferredcites →https://doi.org/10.1063/1.555605openalex-snapshot
Molecular structures of gas-phase polyatomic molecules determined by spectroscopic methods
inferredcites →https://doi.org/10.1080/00268977100103431openalex-snapshot
Asymmetry in the nuclear magnetic shielding tensor
inferredcites →https://doi.org/10.1080/00268977700101851openalex-snapshot
Density-dependent magnetic shielding in gas phase 13C N.M.R.
inferredcites →https://doi.org/10.1080/00268978300100581openalex-snapshot
Theory of magnetic susceptibilities and N.M.R. chemical shifts in terms of localized quantities
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4855750openalex-extracted
Polycycloalkanes at the Helm: Exploring Efuel with Norbornyl Derivatives
inferred← citeshttps://doi.org/10.1002/9780470147283.ch1openalex-snapshot
Molecular Structure and Carbon‐13 Chemical Shielding Tensors Obtained from Nuclear Magnetic Resonance
inferred← citeshttps://doi.org/10.1002/9780470147306.ch3openalex-snapshot
Unusual Saturated Hydrocarbons: Interaction Between Theoretical and Synthetic Chemistry
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0028openalex-snapshot
General and Theoretical Aspects of the Cyclopropyl Group
inferred← citeshttps://doi.org/10.1002/9783527627134.ch2openalex-snapshot
Distorted Saturated Hydrocarbons
inferred← citeshttps://doi.org/10.1002/cber.19891220824openalex-snapshot
Synthesen substituierter [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1002/cber.19911240326openalex-snapshot
Synthesis of Monosubstituted [1.1.1]Propellanes
inferred← citeshttps://doi.org/10.1002/chem.201704105openalex-snapshot
Alkyl and Aryl Thiol Addition to [1.1.1]Propellane: Scope and Limitations of a Fast Conjugation Reaction
inferred← citeshttps://doi.org/10.1002/chin.198614056openalex-snapshot
ChemInform Abstract: Low Temperature 13C NMR in Solids. Part 4. Cyclopropane, Bicyclo[1.1.0]butane and [1.1.1]Propellane.
inferred← citeshttps://doi.org/10.1002/mrc.1260260510openalex-snapshot
Magnetic properties in terms of localized quantities. VIII—Azines and azoles
inferred← citeshttps://doi.org/10.1002/mrc.1260321108openalex-snapshot
Molecular symmetry and shielding tensor properties—some illustrative examples
inferred← citeshttps://doi.org/10.1002/poc.610060803openalex-snapshot
Structure, stabilization energies and chemical shifts of the cyclobutenyl cation. Does it have ‘aromatic’ homocyclopropenium ion character? An ab initio study
inferred← citeshttps://doi.org/10.1002/prac.19973390141openalex-snapshot
Synthesis of [1.1.1]Propellanes by Cyclization of 3-Alkylidenecyclobutylidenes
inferred← citeshttps://doi.org/10.1002/qua.560310106openalex-snapshot
Analysis of the IGLO bond contributions to the 13C shielding tensors in the local bond frame
inferred← citeshttps://doi.org/10.1007/978-3-642-61279-4_8openalex-snapshot
Atoms in Molecular Environments
inferred← citeshttps://doi.org/10.1007/978-3-642-75932-1_3openalex-snapshot
The IGLO-Method: Ab-initio Calculation and Interpretation of NMR Chemical Shifts and Magnetic Susceptibilities
inferred← citeshttps://doi.org/10.1007/978-94-011-1652-7_1openalex-snapshot
An Overview of Nuclear Shielding Calculations
inferred← citeshttps://doi.org/10.1007/978-94-011-1652-7_7openalex-snapshot
The IGLO method. Recent developments
inferred← citeshttps://doi.org/10.1016/0166-1280(88)80028-9openalex-snapshot
Present and future trends in quantum chemical calculations
inferred← citeshttps://doi.org/10.1016/0166-1280(89)87003-4openalex-snapshot
Ab initio calculation of molecular properties
inferred← citeshttps://doi.org/10.1016/0301-0104(88)87213-6openalex-snapshot
Magnetic properties in terms of localized quantities. XI. Fluorine compounds of first-row elements
inferred← citeshttps://doi.org/10.1016/j.jms.2007.12.009openalex-snapshot
High resolution infrared spectroscopy of [1.1.1]propellane
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.theochem.2003.11.039openalex-snapshot
Vibrational frequencies and structural determination of [1.1.1]propellane
inferred← citeshttps://doi.org/10.1016/s0040-4020(97)10276-9openalex-snapshot
Cyclopropanes: Calculation of NMR spectra by ab initio methodology
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)94362-4openalex-snapshot
13C-13C Coupling in [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1016/s0166-1280(03)00243-4openalex-snapshot
Vibrational frequencies and structural determination of bicyclo[1.1.0]butane
inferred← citeshttps://doi.org/10.1021/acs.jctc.5b00752openalex-snapshot
Critical Analysis of Cluster Models and Exchange-Correlation Functionals for Calculating Magnetic Shielding in Molecular Solids
inferred← citeshttps://doi.org/10.1021/acs.jpca.2c06450openalex-snapshot
Magnetic Shielding Analysis of Bonding in [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1021/ar00136a005openalex-snapshot
Carbon-13 shielding tensors: experimental and theoretical determination
inferred← citeshttps://doi.org/10.1021/cr990094zopenalex-snapshot
Bicyclo[1.1.1]pentanes, [ n ]Staffanes, [1.1.1]Propellanes, and Tricyclo[2.1.0.0 2,5 ]pentanes
inferred← citeshttps://doi.org/10.1021/jo990040popenalex-snapshot
Small-Ring GeminanesNew Hypothetical Molecules with Inverted Carbon Atoms
inferred← citeshttps://doi.org/10.1063/1.452419openalex-snapshot
Magnetic properties in terms of localized quantities. VI. Small hydrides, fluorides, and homonuclear molecules of phosphorus and silicon
inferred← citeshttps://doi.org/10.1063/1.471789openalex-snapshot
A comparison of models for calculating nuclear magnetic resonance shielding tensors
inferred← citeshttps://doi.org/10.1080/00268978800100693openalex-snapshot
13C Dipolar spectroscopy of nitromethane
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.