On the public citation graph
[1.1.1]Propellane
0 signed · 298 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known work and none has been retracted — and get a dated CiteStamped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 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/(sici)1097-461x(1996)57:2<183::aid-qua4>3.0.co;2-uopenalex-snapshot
Structural homeomorphism between the electron density and the virial field
inferred← citeshttps://doi.org/10.1002/0471264229.os101.11openalex-snapshot
Intramolecular Coupling for General Synthesis of Backbone Substituted Bicyclo[1.1.1]Pentyl Boronates
inferred← citeshttps://doi.org/10.1002/1097-458x(200007)38:7<551::aid-mrc686>3.0.co;2-qopenalex-snapshot
Fluorine as an NMR probe for structural studies of chemical and biological systems
inferred← citeshttps://doi.org/10.1002/1099-0690(200004)2000:7<1137::aid-ejoc1137>3.0.co;2-2openalex-snapshot
Nickel- and Palladium-Catalyzed Cross-Coupling Reactions at the Bridgehead of Bicyclo[1.1.1]pentane Derivatives - A Convenient Access to Liquid Crystalline Compounds Containing Bicyclo[1.1.1]pentane Moieties
inferred← citeshttps://doi.org/10.1002/9780470147252.ch4openalex-snapshot
Substituent Effects on 13 C Chemical Shifts in Aliphatic Molecular Systems. Dependence on Constitution and Stereochemistry
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.pat0023openalex-snapshot
Eliminations Involving Carbon–Halogen Bonds and Leading to Highly Strained Rings
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0194openalex-snapshot
Cyclic Polychalcogenide Compounds with Silicon
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0337openalex-snapshot
Cubanes, Fenestranes, Ladderanes, Prismanes, Staffanes and Other Oligocyclobutanoids
inferred← citeshttps://doi.org/10.1002/9783527627134.ch2openalex-snapshot
Distorted Saturated Hydrocarbons
inferred← citeshttps://doi.org/10.1002/adsc.70768openalex-snapshot
A New Route to Three‐Dimensional Bioisosteres of Arenes: Pd‐Catalyzed Decarboxylative Cycloadditions for Efficient Construction of Bicyclo[ n .1.1]Alkane Analogues
inferred← citeshttps://doi.org/10.1002/ajoc.201900589openalex-snapshot
Selected Topics in the Syntheses of Bicyclo[1.1.1]Pentane (BCP) Analogues
inferred← citeshttps://doi.org/10.1002/ange.19860980405openalex-snapshot
Das Konzept der Spannung in der Organischen Chemie
inferred← citeshttps://doi.org/10.1002/ange.19870990434openalex-snapshot
Bindungsdehnungsisomerie in Bicyclo[1.1.0]tetrasilanen – das unterschiedliche Verhalten von gespannten Silicium- und Kohlenstoffringen
inferred← citeshttps://doi.org/10.1002/ange.19870991215openalex-snapshot
Reaktionen von 2,2,4,4‐Tetramethyl‐3‐methylen‐cyclobutyliden; thermische Umlagerungen eines 2‐Methylenbicyclo[2.1.0]pentans
inferred← citeshttps://doi.org/10.1002/ange.19911030805openalex-snapshot
Verbindungen mit SiSi‐, GeGe‐ und SnSn‐Doppelbindungen sowie gespannte Ringsysteme mit Si‐, Ge‐ und Sn‐Gerüsten
inferred← citeshttps://doi.org/10.1002/ange.19941060605openalex-snapshot
Die Theoretische Definition einer funktionellen Gruppe und das Paradigma des Molekülorbitals
inferred← citeshttps://doi.org/10.1002/ange.200705775openalex-snapshot
Moleküle in Not – und was wir von ihnen lernen
inferred← citeshttps://doi.org/10.1002/ange.200804965openalex-snapshot
The Inverted Bond in [1.1.1]Propellane is a Charge‐Shift Bond
inferred← citeshttps://doi.org/10.1002/ange.201603951openalex-snapshot
Propellane: von chemischen Kuriositäten zu “explosiven” Materialen und Naturstoffen
inferred← citeshttps://doi.org/10.1002/ange.201810061openalex-snapshot
Synthesis of BCP Benzylamines From 2‐Azaallyl Anions and [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1002/ange.201900824openalex-snapshot
A Tetrasilicon Analogue of Bicyclo[1.1.0]but‐1(3)‐ene Containing a Si=Si Double Bond with an Inverted Geometry
inferred← citeshttps://doi.org/10.1002/ange.201914875openalex-snapshot
1,3‐Difunctionalizations of [1.1.1]Propellane via 1,2‐Metallate Rearrangements of Boronate Complexes
inferred← citeshttps://doi.org/10.1002/ange.202213508openalex-snapshot
Rapid and Scalable Halosulfonylation of Strain‐Release Reagents**
inferred← citeshttps://doi.org/10.1002/ange.202218211openalex-snapshot
On‐Surface Synthesis of Polyphenylene Wires Comprising Rigid Aliphatic Bicyclo[1.1.1]Pentane Isolator Units
inferred← citeshttps://doi.org/10.1002/ange.202513768openalex-snapshot
Rapid and Modular Access to All‐Carbon Quaternary Center‐Containing 2,2‐Disubstituted Bicyclo[1.1.1]pentanes via Cyanocarbene Addition to Bicyclo[1.1.0]butanes
inferred← citeshttps://doi.org/10.1002/anie.198603121openalex-snapshot
The Concept of Strain in Organic Chemistry
inferred← citeshttps://doi.org/10.1002/anie.198703641openalex-snapshot
Bond Stretch Isomerism in Bicyclo[1.1.0]tetrasilanes. Contrasts Between Strained Silicon and Carbon Ring Systems
inferred← citeshttps://doi.org/10.1002/anie.198712601openalex-snapshot
Reactions of 2,2,4,4‐Tetramethyl‐3‐methylenecyclobutylidene; Thermal Rearrangements of a 2‐Methylenebicyclo[2.1.0]pentane
inferred← citeshttps://doi.org/10.1002/anie.199109021openalex-snapshot
Strained‐Ring and Double‐Bond Systems Consisting of the Group 14 Elements Si, Ge, and Sn
inferred← citeshttps://doi.org/10.1002/anie.199406201openalex-snapshot
Theoretical Definition of a Functional Group and the Molecular Orbital Paradigm
inferred← citeshttps://doi.org/10.1002/anie.200705775openalex-snapshot
Learning from Molecules in Distress
inferred← citeshttps://doi.org/10.1002/anie.200804965openalex-snapshot
The Inverted Bond in [1.1.1]Propellane is a Charge‐Shift Bond
inferred← citeshttps://doi.org/10.1002/anie.201603951openalex-snapshot
Propellanes—From a Chemical Curiosity to “Explosive” Materials and Natural Products
inferred← citeshttps://doi.org/10.1002/anie.201810061openalex-snapshot
Synthesis of BCP Benzylamines From 2‐Azaallyl Anions and [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1002/anie.201900824openalex-snapshot
A Tetrasilicon Analogue of Bicyclo[1.1.0]but‐1(3)‐ene Containing a Si=Si Double Bond with an Inverted Geometry
inferred← citeshttps://doi.org/10.1002/anie.201914875openalex-snapshot
1,3‐Difunctionalizations of [1.1.1]Propellane via 1,2‐Metallate Rearrangements of Boronate Complexes
inferred← citeshttps://doi.org/10.1002/anie.202213508openalex-snapshot
Rapid and Scalable Halosulfonylation of Strain‐Release Reagents**
inferred← citeshttps://doi.org/10.1002/anie.202218211openalex-snapshot
On‐Surface Synthesis of Polyphenylene Wires Comprising Rigid Aliphatic Bicyclo[1.1.1]Pentane Isolator Units
inferred← citeshttps://doi.org/10.1002/anie.202513768openalex-snapshot
Rapid and Modular Access to All‐Carbon Quaternary Center‐Containing 2,2‐Disubstituted Bicyclo[1.1.1]pentanes via Cyanocarbene Addition to Bicyclo[1.1.0]butanes
inferred← citeshttps://doi.org/10.1002/asia.202300903openalex-snapshot
Heavy Tetrel Clusters Based on the Bicyclobutane Framework: Bicyclo[1.1.0]butanes, [1.1.1]Propellanes, and Tricyclo[2.1.0.02,5]pentanes
inferred← citeshttps://doi.org/10.1002/cber.19851180727openalex-snapshot
Zur Chemie einiger [4.1.1]‐ und [3.1.1]Propellane
inferred← citeshttps://doi.org/10.1002/cber.19881211014openalex-snapshot
Brückenkopf‐gekoppelte Bicyclo[1.1.1]pentane: Synthese und Struktur
inferred← citeshttps://doi.org/10.1002/cber.19891220233openalex-snapshot
Concerning the Synthesis of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1002/cber.19891220824openalex-snapshot
Synthesen substituierter [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1002/cber.19921250332openalex-snapshot
Kurzmitteilung/Short Communication Solvent‐Free [1.1.1]Propellane from 1,3‐Diiodobicyclo[1.1.1]pentane
inferred← citeshttps://doi.org/10.1002/chem.200500049openalex-snapshot
Heavy Group 14 1,(n+2)‐Dimetallabicyclo[n.n.n]alkanes and 1,(n+2)‐Dimetalla[n.n.n]propellanes: Are They All Realistic Synthetic Targets?
inferred← citeshttps://doi.org/10.1002/chem.200800914openalex-snapshot
XX Through‐Cage Bonding in Cu, Ni, and Cr Complexes with M3X2 Cores (X=S, As)
inferred← citeshttps://doi.org/10.1002/chem.200900239openalex-snapshot
A Bonding Quandary—or—A Demonstration of the Fact That Scientists Are Not Born With Logic
inferred← citeshttps://doi.org/10.1002/chem.201400143openalex-snapshot
New PN Cage Compounds Generated by Small‐Molecule Activation
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/chem.201904910openalex-snapshot
The “Inverted Bonds” Revisited: Analysis of “In Silico” Models and of [1.1.1]Propellane by Using Orbital Forces
inferred← citeshttps://doi.org/10.1002/chem.202304070openalex-snapshot
Organometallic Bridge Diversification of Bicyclo[1.1.1]pentanes
inferred← citeshttps://doi.org/10.1002/chem.202402152openalex-snapshot
Uncatalyzed Diboron Activation by a Strained Hydrocarbon: Experimental and Theoretical Study of [1.1.1]Propellane Diborylation
inferred← citeshttps://doi.org/10.1002/chin.198251221openalex-snapshot
ChemInform Abstract: (1.1.1)PROPELLANE
inferred← citeshttps://doi.org/10.1002/cphc.200900633openalex-snapshot
An Excursion from Normal to Inverted CC Bonds Shows a Clear Demarcation between Covalent and Charge‐Shift CC Bonds
inferred← citeshttps://doi.org/10.1002/cphc.201402184openalex-snapshot
The Local Kinetic Energy Profile of an Inverted CarbonCarbon Bond Reveals and Refines its Charge‐Shift Character
inferred← citeshttps://doi.org/10.1002/cphc.201600632openalex-snapshot
Tracing the Fingerprint of Chemical Bonds within the Electron Densities of Hydrocarbons: A Comparative Analysis of the Optimized and the Promolecule Densities
inferred← citeshttps://doi.org/10.1002/cphc.202300875openalex-snapshot
When, Where and Why Boron Prefers Boron to Nitrogen
inferred← citeshttps://doi.org/10.1002/ejoc.200400121openalex-snapshot
Dihaloadamantanes: Ring Closure versus Rearrangement or Halogen‐Displacement Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.201701296openalex-snapshot
Bicyclo[1.1.1]pentane‐Derived Building Blocks for Click Chemistry
inferred← citeshttps://doi.org/10.1002/ejoc.202000303openalex-snapshot
3‐Carboxy‐/3‐Aminobicyclo[1.1.1]pentane‐Derived Sulfonamides and Sulfonyl Fluorides – Advanced Bifunctional Reagents for Organic Synthesis and Drug Discovery
inferred← citeshttps://doi.org/10.1002/hlca.19880710827openalex-snapshot
Crystal Structure and Electron‐Density Distribution of Two [1.1.1] Propellane Derivatives at 81 K
inferred← citeshttps://doi.org/10.1002/hlca.19900730603openalex-snapshot
The crystal structure of [1.1.1]propellane at 138 K
inferred← citeshttps://doi.org/10.1002/hlca.19930760303openalex-snapshot
Structural chemistry in Helvetica Chimica Acta, 1917–1992
inferred← citeshttps://doi.org/10.1002/ijch.201500013openalex-snapshot
Physical Organic Chemistry by Any Other Name Would Smell as Sweet
inferred← citeshttps://doi.org/10.1002/ijch.201700085openalex-snapshot
Organic Synthesis: Wherefrom and Whither? (Some Very Personal Reflections)
inferred← citeshttps://doi.org/10.1002/jcc.10343openalex-snapshot
Bond energies for molecules, clusters, and deposit systems
inferred← citeshttps://doi.org/10.1002/jcc.20615openalex-snapshot
New insights on the bridge carbon–carbon bond in propellanes: A theoretical study based on the analysis of the electron localization function
inferred← citeshttps://doi.org/10.1002/jcc.540050608openalex-snapshot
A unified treatment of valence and bond order from density operators
inferred← citeshttps://doi.org/10.1002/jcc.540050610openalex-snapshot
Classical conformational analysis of strained organic molecules. I. [l,m,n]Propellanes with l,m,n equal to 2, 3, and 4
inferred← citeshttps://doi.org/10.1002/jcc.540060602openalex-snapshot
Comparative studies on the reactivity of molecules by atomic valences
inferred← citeshttps://doi.org/10.1002/jlac.199619961103openalex-snapshot
Synthesis of [1.1.1]Propellanes by Bridging of Bicyclo[1.1.0]butanes
inferred← citeshttps://doi.org/10.1002/macp.1991.021921101openalex-snapshot
[1.1.1]Propellanes. From a hydrocarbon curiosity to a versatile monomer for the synthesis of structurally new polymers
inferred← citeshttps://doi.org/10.1002/masy.200750406openalex-snapshot
Spontaneous Copolymerization of 1,3‐Dehydroadamantane
inferred← citeshttps://doi.org/10.1002/mrc.1135openalex-snapshot
Non‐empirical calculations of NMR indirect carbon–carbon coupling constants: 2. Strained polycarbocycles
inferred← citeshttps://doi.org/10.1002/mrc.1312openalex-snapshot
Non‐empirical calculations of NMR indirect carbon–carbon coupling constants. Part 6: Propellanes
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/nadc.19860340418openalex-snapshot
Von Propellanen zu Antipellanen
inferred← citeshttps://doi.org/10.1002/nadc.201490416openalex-snapshot
Die Ästhetik der [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1002/poc.3391openalex-snapshot
Approach to Loschmidt's tetracyclic benzene isomer and related tetra‐ and tricyclic isomers by intramolecular carbene additions
inferred← citeshttps://doi.org/10.1002/poc.4019openalex-snapshot
Switchable dual bonding nature in silabicyclo[1.1.0]butanes that exhibit bond stretch isomerism
inferred← citeshttps://doi.org/10.1002/poc.4644openalex-snapshot
Paddlanes revisited: Which are the smallest possible?
inferred← citeshttps://doi.org/10.1002/poc.70088openalex-snapshot
Undergraduate Research in Computational Physical Organic Chemistry: Unleashing the Predictive Power of Nonstationary Points
inferred← citeshttps://doi.org/10.1002/pola.26820openalex-snapshot
Cationic ring-opening polymerization of novel 1,3-dehydroadamantanes with various alkyl substituents: Synthesis of thermally stable poly(1,3-adamantane)s
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.560382462openalex-snapshot
Average local ionization energies computed on the surfaces of some strained molecules
inferred← citeshttps://doi.org/10.1002/slct.202302714openalex-snapshot
Re‐establishing the Lost Covalency of the Inverted Bond in [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1007/3-540-45731-3_1openalex-snapshot
Diphosphorus-Containing Unsaturated Three-Membered Rings: Comparison of Carbon, Nitrogen, and Phosphorus Chemistry
inferred← citeshttps://doi.org/10.1007/3-540-52422-3_2openalex-snapshot
Gem-Dihalocyclopropanes in organic synthesis
inferred← citeshttps://doi.org/10.1007/978-1-4020-6973-4_12openalex-snapshot
Polyprismanes. Flights of Fun and Fancy
inferred← citeshttps://doi.org/10.1007/978-1-4020-6973-4_13openalex-snapshot
A Menagerie of Molecules from Michl and Balaji: Superstrained Molecules
inferred← citeshttps://doi.org/10.1007/978-1-4613-9795-3_1openalex-snapshot
Chemical Bonding and Structure
inferred← citeshttps://doi.org/10.1007/978-3-031-97743-5_11openalex-snapshot
Exploring Variation in Bonding and Structure for Tetravalent Carbon: [1.1.1]Propellane and Inverted Carbon
inferred← citeshttps://doi.org/10.1007/978-3-642-49348-5_5openalex-snapshot
Organometallic-Aided “SO”, “S2” and “S” Transfer in the Synthesis of Small-Membered Heterocycles
inferred← citeshttps://doi.org/10.1007/978-3-642-61277-0_3openalex-snapshot
Valence in Molecular Orbital Theory
inferred← citeshttps://doi.org/10.1007/978-3-642-61277-0_8openalex-snapshot
Properties of the Fermi Hole and Electronic Localization
inferred← citeshttps://doi.org/10.1007/978-3-642-93239-7_13openalex-snapshot
Why “Effective” Bonds exist when “Real” Bonds are Absent: The Electronic Structure of the (1.1.1.) Propellane
inferred← citeshttps://doi.org/10.1007/978-94-009-0929-8_24openalex-snapshot
From Bicyclo[1.1.0]Butanes to [n.1.1]Propellanes
inferred← citeshttps://doi.org/10.1007/978-94-009-2853-4_7openalex-snapshot
A Valence Concept for Molecular Structure and Reactions
inferred← citeshttps://doi.org/10.1007/978-94-011-0005-2_5openalex-snapshot
Supramolecular Assemblies from “Tinkertoy” Rigid-Rod Molecules
inferred← citeshttps://doi.org/10.1007/978-94-011-0337-4_14openalex-snapshot
The “Molecular Tinkertoy” Approach to Materials
inferred← citeshttps://doi.org/10.1007/978-94-011-3214-5_9openalex-snapshot
The Molecular and Electronic Structure of Polycyclic Polystannanes
inferred← citeshttps://doi.org/10.1007/bf00173470openalex-snapshot
On the use of isovalued surfaces to determine molecule shape and reaction pathways
inferred← citeshttps://doi.org/10.1007/bf00527667openalex-snapshot
Low temperature 13C NMR magnetic resonance in solids 4. Cyclopropane, bicyclo[1.1.0]butane and [1.1.1] propellane
inferred← citeshttps://doi.org/10.1007/bf00951063openalex-snapshot
Quantum-chemical analysis of the structure of strained molecules. Communication 4. [n.1.1]propellanes
inferred← citeshttps://doi.org/10.1007/bf00953743openalex-snapshot
Electrophilic cleavage of [1.1.1]-propellane by triorganoboranes
inferred← citeshttps://doi.org/10.1007/bf00957272openalex-snapshot
Addition of halogens to [1.1.1]propellane
inferred← citeshttps://doi.org/10.1007/bf01437446openalex-snapshot
Topological models of the chemical bonding in transition metal-silicon clusters
inferred← citeshttps://doi.org/10.1007/s00214-009-0563-7openalex-snapshot
An overview of the electronic structure in trigonal bipyramidal clusters of main elements or mixed with transition metals
inferred← citeshttps://doi.org/10.1007/s00214-023-02966-1openalex-snapshot
DFT calculations predict that inverted geometries at carbon can be stabilized within multi-component co-crystals
inferred← citeshttps://doi.org/10.1007/s11224-010-9656-0openalex-snapshot
Interplay of thermochemistry and Structural Chemistry, the journal (volume 20, 2009) and the discipline
inferred← citeshttps://doi.org/10.1007/s11426-025-3149-2openalex-snapshot
Controlled ring-opening of [1.1.1]propellane with aryl catecholato boronates to form monomeric and dimeric methylenecyclobutanes
inferred← citeshttps://doi.org/10.1007/s41061-025-00490-3openalex-snapshot
Recent Advances in Radical Coupling Reactions Directly Involving Bicyclo[1.1.1]pentane (BCP)
inferred← citeshttps://doi.org/10.1016/0009-2614(92)85465-mopenalex-snapshot
Long bonds in silicon clusters: a failure of conventional Møller—Plesset perturbation theory?
inferred← citeshttps://doi.org/10.1016/0009-2614(96)00415-0openalex-snapshot
Origin of the bridge bond in [1,1,1]propellane
inferred← citeshttps://doi.org/10.1016/0020-1693(95)04556-2openalex-snapshot
The synthesis and structural characterization of carborane oligomers connected by carbon-carbon and carbon-boron bonds between icosahedra
inferred← citeshttps://doi.org/10.1016/0022-2860(89)80076-6openalex-snapshot
Geometry changes induced by negative hyperconjugative interactions involving carbonyl and thiocarbonyl groups
inferred← citeshttps://doi.org/10.1016/0022-328x(96)06121-9openalex-snapshot
Synthesis and reactions of polythiadisilabicyclo[k.l.m.]alkanes
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00912-xopenalex-snapshot
Competing 1,n-elimination reactions of 1-Bromo-5-bromomethyl-6,6-dichlorobicyclo[3.1.0]hexane: A strained 1,3-bridged cyclopropene and a vinylcarbene as reactive intermediates
inferred← citeshttps://doi.org/10.1016/0166-1280(86)80062-8openalex-snapshot
[1.1.1]Propellane, bicyclo[1.1.1]pentane and the effects of “inverted” carbons
inferred← citeshttps://doi.org/10.1016/0166-1280(86)85009-6openalex-snapshot
A novel interpretation of bonding in [1.1.1] propellane and theoretical calculation of its unimolecular rearrangement
inferred← citeshttps://doi.org/10.1016/0166-1280(90)85067-wopenalex-snapshot
1,3-Diphosphabicyclo[1.1.1]pentane dication: theoretical evidence for an inverted phosphorus atom
inferred← citeshttps://doi.org/10.1016/0166-1280(91)90042-iopenalex-snapshot
An AB initio gradient study of the molecular geometry of some strained hydrocarbons containing annelated three-membered rings
inferred← citeshttps://doi.org/10.1016/0166-1280(92)85022-dopenalex-snapshot
Experimental vs. theoretical topological properties of charge density distributions. An application to the l-alanine molecule studied by X-ray diffraction at 23 K
inferred← citeshttps://doi.org/10.1016/0166-1280(92)87057-7openalex-snapshot
The molecular structure of pentastanna[1.1.1]propellane and bicyclo[1.1.1]pentastannane from the quasi-relativistic SIC-MS-Xα theory
inferred← citeshttps://doi.org/10.1016/0166-1280(94)85002-xopenalex-snapshot
Orismology (the science of defining words) and the geometrical foundations of chemistry Part 1. Introduction
inferred← citeshttps://doi.org/10.1016/0166-1280(95)04348-9openalex-snapshot
Orismology (the science of defining words) and the geometrical foundations of chemistry Part 3. What constitutes a ring?
inferred← citeshttps://doi.org/10.1016/0168-1176(92)85068-bopenalex-snapshot
The chemistry of gas-phase ions: a theoretical approach
inferred← citeshttps://doi.org/10.1016/b978-0-08-034481-2.50009-9openalex-snapshot
TOOLS OF OUR TRADE
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00311-6openalex-snapshot
3.07 Coupling Reactions Between sp3-Carbon Centers
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00118-2openalex-snapshot
Main Group Biradicaloids
inferred← citeshttps://doi.org/10.1016/b978-0-12-813651-5.00007-3openalex-snapshot
Personal computers in computational chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-12-821062-8.00010-7openalex-snapshot
Conformations of cyclic, fused and bridged ring molecules
inferred← citeshttps://doi.org/10.1016/b978-0-444-88871-6.50022-2openalex-snapshot
The chemistry of gas-phase ions: a theoretical approach
inferred← citeshttps://doi.org/10.1016/b978-044451685-5/50003-2openalex-snapshot
Other significant differences from existing systems
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.04.023openalex-snapshot
Recent advances in the applications of [1.1.1]propellane in organic synthesis
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.11.027openalex-snapshot
HSH-C10: A new quasi-2D carbon allotrope with a honeycomb-star-honeycomb lattice
inferred← citeshttps://doi.org/10.1016/j.comptc.2012.03.006openalex-snapshot
A molecule containing a stable carbon atom with all four bonds directed toward the same side of the nucleus
inferred← citeshttps://doi.org/10.1016/j.comptc.2013.12.020openalex-snapshot
Structures and electronic properties of lantern-like molecule BGe3H6N and its polymers
inferred← citeshttps://doi.org/10.1016/j.comptc.2021.113505openalex-snapshot
Dependence of hydrocarbon sigma CC bond strength on bond angles: The concepts of “inverted”, “direct” and “superdirect” bonds
inferred← citeshttps://doi.org/10.1016/j.ica.2009.06.019openalex-snapshot
Syntheses and characterization of iron(II) and iron(III) complexes of a tripodal ligand derived from tris(2-aminoethyl)methane
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.jms.2008.09.013openalex-snapshot
High-resolution rovibrational study of the Coriolis-coupled ν12 and ν15 modes of [1.1.1]propellane
inferred← citeshttps://doi.org/10.1016/j.jms.2010.04.010openalex-snapshot
High-resolution infrared spectra of bicyclo[1.1.1]pentane
inferred← citeshttps://doi.org/10.1016/j.jms.2012.09.001openalex-snapshot
High-resolution infrared studies of the ν10, ν11, ν14, and ν18 levels of [1.1.1]propellane
inferred← citeshttps://doi.org/10.1016/j.molstruc.2011.11.044openalex-snapshot
Molecular and crystal structure of selected compounds containing 8,11-dioxa[4.3.3]propellane moiety
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.pnmrs.2018.03.001openalex-snapshot
Carbon-carbon spin-spin coupling constants: Practical applications of theoretical calculations
inferred← citeshttps://doi.org/10.1016/j.tet.2005.01.066openalex-snapshot
Highly strained tricyclic molecules: tricyclo[p.q.0.01,f]alkanes and phosphatricyclo[m.1.0.01,3]alkanes
inferred← citeshttps://doi.org/10.1016/j.tet.2005.06.013openalex-snapshot
Synthesis of propellane-containing natural products
inferred← citeshttps://doi.org/10.1016/j.tet.2013.02.042openalex-snapshot
Synthesis and ring-opening reaction of novel 1,3-dehydroadamantanes possessing phenyl and alkoxyl substituents
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/s0022-1139(02)00155-0openalex-snapshot
Synthesis of 1,3-bis(N,N-difluoroamino)adamantane: addition of difluoramino radicals to 1,3-dehydroadamantane
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)80581-0openalex-snapshot
Synthesis and reactivity of [3.1.1] and [2.1.1]silapropellanes
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)80896-6openalex-snapshot
General approach for the synthesis of polyquinenes via the Weiss reaction
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)81354-5openalex-snapshot
Intrabrigehead chemistry
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)87604-3openalex-snapshot
Synthesis of some [4.1.1]- and [3.1.1]propellanes with silicon, phosphorus, sulfur, titanium, germanium, or tin in the long bridge
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)96479-8openalex-snapshot
Evaluation of the effect of strain upon reactivity
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)96746-8openalex-snapshot
n-n orbital interaction involving σ-aromaticity
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)85341-1openalex-snapshot
Thermal rearrangement of some [1.1.1] propellanes
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)86105-5openalex-snapshot
General approach to the synthesis of polyquinenes VII. Synthesis of a centro-substituted triquinacene
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)89157-1openalex-snapshot
Origin of strain in bicyclo[1.1.1]pentane
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)91764-7openalex-snapshot
Reaction of phenylchlorocarbene with [1.1.1] propellane: Absolute rate constants and mechanism
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/s0040-4039(00)94592-1openalex-snapshot
Reduction of [1.1.1]propellane with lithium 4,4′-Di-t-butylbiphenyl: Bicyclo[1.1.1]pent-1,3-diyldilithium
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)95226-2openalex-snapshot
Towards a molecular-size construction set: 3,3(n-1)-bisacetylthio[n]staffanes
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)96295-6openalex-snapshot
Tetracyclo[5.1.0.01,6.02,7]octane: some unexpected addition reactions and a new synthesis
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)97847-xopenalex-snapshot
Unusual bridgehead reactivity: Formation of [1.1.1]Propellane by 1,3-dehydrobromination of 1-bromobicyclo[1.1.1]Pentane.
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)93718-9openalex-snapshot
Synthesis of 1-alkynylbicyclo[1.1.1]pentanes
inferred← citeshttps://doi.org/10.1016/s0066-4103(07)61103-xopenalex-snapshot
Recent Advances in Theoretical Calculations of Indirect Spin–Spin Coupling Constants
inferred← citeshttps://doi.org/10.1016/s0166-1280(97)00382-5openalex-snapshot
Redefining the terminology of stereoisomerism to produce a mathematics-based taxonomy paradigm
inferred← citeshttps://doi.org/10.1016/s0166-1280(99)00048-2openalex-snapshot
Graph theoretical logic of organic chemistry nomenclature: why Eulerian paths are better suited for aliphatic compounds versus Hamiltonian paths for benzenoids
inferred← citeshttps://doi.org/10.1016/s0277-5387(00)86102-1openalex-snapshot
The structure and bonding in group IV [1.1.1]Propellanes
inferred← citeshttps://doi.org/10.1016/s1380-7323(07)80009-4openalex-snapshot
Chapter 8 The average local ionization energy: concepts and applications
inferred← citeshttps://doi.org/10.1016/s1380-7323(98)80009-5openalex-snapshot
Average local ionization energies: Significance and applications
inferred← citeshttps://doi.org/10.1016/s1380-7323(99)80012-0openalex-snapshot
Bond energies, enthalpies of formation, and homologies: the energetics of aliphatic and alicyclic hydrocarbons and some of their derivatives
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00052openalex-snapshot
Molecular Silicon Clusters
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00187openalex-snapshot
Increase in Strain Energy during Conversion of [4.4.4.5]Fenestrane to [4.4.4.4]Fenestrane: a Method for Estimating the Heats of Formation of Hydrocarbons and Their Derivatives from Ab Initio Energies
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00977openalex-snapshot
Large-Scale Synthesis and Modifications of Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid (BCP)
inferred← citeshttps://doi.org/10.1021/acs.jpca.5c03794openalex-snapshot
Questioning the Central Bond in [1.1.1]Propellane: Insights from Probability Density Analysis
inferred← citeshttps://doi.org/10.1021/acs.oprd.0c00156openalex-snapshot
Applications of Flow Chemistry in the Pharmaceutical Industry—Highlights of the Recent Patent Literature
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00521openalex-snapshot
Reduction of a Bicyclo[1.1.0]tetrasil-1(3)-ene with LiAlH4 Leading to an Isolable Cyclotrisilenide
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02017openalex-snapshot
Iridium-Catalyzed Enantioselective Synthesis of α-Chiral Bicyclo[1.1.1]pentanes by 1,3-Difunctionalization of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02790openalex-snapshot
Synthesis of Imidized Cyclobutene Derivatives by Strain Release of [1.1.1]Propellane
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01417openalex-snapshot
Synthesis of Bicyclo[1.1.0]butanes from Iodo-Bicyclo[1.1.1]pentanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01645openalex-snapshot
Stellane at the Forefront: Derivatization and Reactivity Studies of a Promising Saturated Bioisostere of ortho -Substituted Benzenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04750openalex-snapshot
Synthesis of Carborane-Fused Lactones via Electrochemical C( sp 3 )–H Lactonization: Access to Benzofused Lactone Bioisosteres
showing the first 200 of 298 · page through all 298
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.