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RICONThe Computer Program for the Quantitative Investigations of Cyclic Organic Molecule Conformations

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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/chin.198025064openalex-snapshot

ChemInform Abstract: CONFORMATION AND STRUCTURE OF CYCLO‐(DIBENZYLGLYCYL‐L‐PROLINE) AND CYCLO‐(DI‐L‐PROLYL‐D‐PROLINE) IN THE CRYSTALLINE STATE

inferredcites →https://doi.org/10.1002/ijch.198300010openalex-snapshot

Theoretical Determination of Molecular Structure and Conformation. XI. The Puckering of Oxolanes

inferredcites →https://doi.org/10.1002/poc.610030304openalex-snapshot

Stereochemical studies. XXXIV. Quantitative description of ring puckering via torsional angles. The case of six‐membered rings

inferredcites →https://doi.org/10.1007/bf01200485openalex-snapshot

The conformation of six-membered rings

inferredcites →https://doi.org/10.1007/bf01209549openalex-snapshot

Identification of the conformational type of seven-membered rings

inferredcites →https://doi.org/10.1016/0022-2860(81)80094-4openalex-snapshot

Conformations of eight-membered cyclosiloxanes

inferredcites →https://doi.org/10.1016/s0008-6215(00)84786-2openalex-snapshot

Stereographic representation of the cremer-pople ring-puckering parameters for pyranoid rings

inferredcites →https://doi.org/10.1016/s0040-4020(01)93869-4openalex-snapshot

Approximate relationships between conformational parameters in 5- and 6-membered rings

inferredcites →https://doi.org/10.1016/s0040-4039(00)70735-0openalex-snapshot

Conformation of non-aromatic ring compounds, Part L boat/twist-boat pseudorotation in six-membered ring compounds

inferredcites →https://doi.org/10.1016/s0040-4039(00)71589-9openalex-snapshot

The relations between torsional and valency angles of cyclopentane

inferredcites →https://doi.org/10.1021/ci00009a001openalex-snapshot

Automatic assignment of chemical connectivity to organic molecules in the Cambridge Structural Database

inferredcites →https://doi.org/10.1021/ci00063a007openalex-snapshot

Review of ring perception algorithms for chemical graphs

inferredcites →https://doi.org/10.1021/ci00063a008openalex-snapshot

Theoretical aspects of ring perception and development of the extended set of smallest rings concept

inferredcites →https://doi.org/10.1021/ja00029a013openalex-snapshot

The conformation of six-membered rings described by puckering coordinates derived from endocyclic torsion angles

inferredcites →https://doi.org/10.1021/ja00029a014openalex-snapshot

Kinetic models for gas-phase electron-transfer reactions between nitrobenzenes

inferredcites →https://doi.org/10.1021/ja00057a034openalex-snapshot

Conformational analysis of six-membered rings in solution: ring puckering coordinates derived from vicinal NMR proton-proton coupling constants

inferredcites →https://doi.org/10.1021/ja00057a035openalex-snapshot

Polarizability and nuclear shielding for the sodium anion in condensed phases

inferredcites →https://doi.org/10.1021/ja00839a011openalex-snapshot

General definition of ring puckering coordinates

inferredcites →https://doi.org/10.1021/ja00839a012openalex-snapshot

Molecular orbital theory of the electronic structure of organic compounds. XXIII. Pseudorotation in saturated five-membered ring compounds

inferredcites →https://doi.org/10.1021/ja00839a013openalex-snapshot

Interrelation of bond dissociation energies and contributing bond energies

inferredcites →https://doi.org/10.1021/ja01002a036openalex-snapshot

Molecular geometry. V. Evaluation of functions and conformations of medium rings

inferredcites →https://doi.org/10.1021/ja01002a038openalex-snapshot

Molecular geometry. VII. Modes of interconversion in the medium rings

inferredcites →https://doi.org/10.1021/ja01076a027openalex-snapshot

Molecular Geometry. IV. The Medium Rings

inferredcites →https://doi.org/10.1021/ja01076a028openalex-snapshot

Strained Ring Systems. I. Peroxidation Studies with Certain Acetylenes. The Relevance of Oxirene Intermediates

inferredcites →https://doi.org/10.1021/ja01202a069openalex-snapshot

The Thermodynamics and Molecular Structure of Cyclopentane 1

inferredcites →https://doi.org/10.1021/ja01202a070openalex-snapshot

The Thermodynamic Properties and Molecular Structure of Cyclohexane, Methylcyclohexane, Ethylcyclohexane and the Seven Dimethylcyclohexanes1

inferredcites →https://doi.org/10.1021/ja01483a012openalex-snapshot

Contraction of Medium Size Rings1

inferredcites →https://doi.org/10.1063/1.1670007openalex-snapshot

Consistent Force Field for Calculations of Conformations, Vibrational Spectra, and Enthalpies of Cycloalkane and n -Alkane Molecules

inferredcites →https://doi.org/10.1063/1.1675525openalex-snapshot

Symmetry and Conformation of the Cycloalkanes

inferredcites →https://doi.org/10.1107/s0108270188005992openalex-snapshot

Functionalized hydrocarbons with condensed ring skeletons. I. Tricyclo[7.4.0.02,6]tridecane skeleton

inferredcites →https://doi.org/10.1107/s0108768184002548openalex-snapshot

On the correct usage of the Cremer–Pople puckering parameters as quantitative descriptors of ring shapes – a reply to recent criticism by Petit, Dillen and Geise

inferredcites →https://doi.org/10.1107/s0108768189008189openalex-snapshot

Group theory of ring pucker

inferredcites →https://doi.org/10.1107/s0108768189008190openalex-snapshot

Conformational analysis of ring pucker

inferredcites →https://doi.org/10.1107/s0108768190000878openalex-snapshot

The conformation of nine-membered rings

inferredcites →https://doi.org/10.1107/s0567740882010036openalex-snapshot

Substituent effects and the in-plane distortion of aromatic rings: a group-theoretical approach

inferredcites →https://doi.org/10.1107/s0567740882010048openalex-snapshot

Structural studies of benzene derivatives. XI. The structure of p-toluidine hydrochloride

inferredcites →https://doi.org/10.1515/zna-1981-0512openalex-snapshot

Molecular Orbital Theory of the Electronic Structure of Organic Compounds

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Total Synthesis, Molecular Editing and Evaluation of a Tripyrrolic Natural Product: The Case of “Butylcycloheptylprodigiosin”

inferred← citeshttps://doi.org/10.1002/chin.199745282openalex-snapshot

ChemInform Abstract: RICON — The Computer Program for the Quantitative Investigations of Cyclic Organic Molecule Conformations

inferred← citeshttps://doi.org/10.1002/ejoc.201500876openalex-snapshot

Furyl‐Substituted Mixed Phosphonium–Iodonium Ylides in the Synthesis of Annelated P‐Containing Heterocyclic Compounds

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Synthesis and x-ray study of novel azofurazan-annulated macrocyclic lactams

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DFT and NMR parameterized conformation of valeranone

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Conformational evaluation and detailed 1H and 13C NMR assignments of eremophilanolides

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Computerized Molecular Modeling of Carbohydrates

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Conformational analysis of tetrahydrofuran and tetrahydrothiopene using 1H NMR spectroscopy and ab initio calculations

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Investigations in the field of benzoxa- zines. 15*. Tandem heterocyclizations with the participion of 2-formylbenzoic acid. The synthesis of isoindolo[1,2-b][1, 3]- and -[2,1-a][1, 3]benzoxazinones

inferred← citeshttps://doi.org/10.1007/s10947-007-0180-zopenalex-snapshot

Structure of methyl-7-methoxy-7-phenyl-6-endo-halobicyclo[3.1.1]heptane-6-exo-carboxylate diastereomers in single crystals

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On the spatial structure of methyl 6,7-endo, sin-dibrom-7-anti-(phenylsulfonyl) bicyclo[3.1.1]heptane-6-exo-carboxylate

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Formation of Isomeric 3-Azabicyclo[3.3.1]nonanes in a Reaction of 1-(2-Hydroxyethoxy)-2,4-dinitrobenzene with Sodium Borohydride, Formaldehyde, and Methylamine

inferred← citeshttps://doi.org/10.1007/s11224-007-9168-8openalex-snapshot

Molecular and crystal structure of ethylene acetal of endo-endo-3-trityloxymethylbicyclo[3.3.1]nonane-2-on-7-ol

inferred← citeshttps://doi.org/10.1007/s11224-007-9174-xopenalex-snapshot

Molecular and crystal structure of indole derivatives fused with substituted bicyclo[3.3.1]nonane

inferred← citeshttps://doi.org/10.1016/j.mencom.2009.01.004openalex-snapshot

Synthesis of indole derivatives fused with bicyclo[3.2.1]octane framework

inferred← citeshttps://doi.org/10.1016/j.mencom.2011.09.005openalex-snapshot

Molecular and crystal structures of hetero-analogues of bicyclo[3.3.1]nonane with nitrogen and sulfur atoms

inferred← citeshttps://doi.org/10.1016/j.mencom.2012.03.007openalex-snapshot

Synthesis and biological testing of conformationally restricted serotonin analogues with bridgehead moieties

inferred← citeshttps://doi.org/10.1016/j.mencom.2014.11.021openalex-snapshot

Synthesis of 5-hydroxy-4-methoxytricyclo[7.3.1.02,7]trideca-2,4,6-trien- 8-one – precursor of putative bioisosteric colchicine analogues

inferred← citeshttps://doi.org/10.1016/j.mencom.2020.03.004openalex-snapshot

New compounds with 4-azatricyclo[4.3.1.13,8]undecane framework

inferred← citeshttps://doi.org/10.1016/j.molstruc.2005.12.017openalex-snapshot

DFT molecular modeling and NMR conformational analysis of a new longipinenetriolone diester

inferred← citeshttps://doi.org/10.1016/j.molstruc.2006.04.028openalex-snapshot

DFT, solution, and crystal conformation of eremophilanolides

inferred← citeshttps://doi.org/10.1016/j.poly.2005.02.024openalex-snapshot

Synthesis and characterization of new di-n-butyl[bis{dimethyl-2-(3-oxo-5-phenyl(4-subtituted)penten-5-ato)malonates}]tin(IV): The crystal structure of di-n-butyl[bis{dimethyl-2-[5-(4-nitrophenyl)-3-oxo-penten-5-ato]malonate}]tin(IV)

inferred← citeshttps://doi.org/10.1021/jo101993aopenalex-snapshot

Photochemical Synthesis of Phosphinolines from Phosphonium−Iodonium Ylides

inferred← citeshttps://doi.org/10.1021/jo501380yopenalex-snapshot

symm-Tetramethylenecyclooctane: En Route to Polyspirocycles

inferred← citeshttps://doi.org/10.1021/jo901984qopenalex-snapshot

Heterocycles from Phosphonium−Iodonium Ylides. Photochemical Synthesis of λ5-Phosphinolines

inferred← citeshttps://doi.org/10.1021/jo991297qopenalex-snapshot

X-ray Crystallographic Study of Substituted Perhydropyrimidinones. Extreme Changes in Ring Conformation

inferred← citeshttps://doi.org/10.1023/b:rujo.0000013133.63685.caopenalex-snapshot

Aminomethylation by Formaldehyde and Primary Amines of Anionic σσ-Adduct Obtained from 2,4-Dinitrophenol and Acetophenone Carbanion

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3-Azabicyclo[3.3.1]nonane Derivatives: VIII. Synthesis and Properties of 6(7)-R-3,3-Dimethyl-1,5- dinitro-3-azoniabicyclo[3.3.1]non-6-ene Iodides

inferred← citeshttps://doi.org/10.1039/c4ra03410dopenalex-snapshot

The dynamics of the conformational changes in the hexopyranose ring: a transition path sampling approach

inferred← citeshttps://doi.org/10.1063/5.0315467openalex-snapshot

A general method for constructing and searching conformations in molecular rings: From Cremer–Pople coordinates to 3D geometries

inferred← citeshttps://doi.org/10.1107/s0108270113023792openalex-snapshot

Two seven-membered heterocycles with 1,2-diaza ring N atoms: 3,5,7-triphenyl-1,2-diazacyclohepta-1(7),2-diene and 3,7-bis(2-hydroxyphenyl)-5-phenyl-1,2-diazacyclohepta-1(7),2-diene

inferred← citeshttps://doi.org/10.1107/s160053680202041xopenalex-snapshot

3-Methyl-1,5-dinitro-9-phenacyl-3-azabicyclo[3.3.1]non-7-en-6-one

inferred← citeshttps://doi.org/10.1107/s1600536810053146openalex-snapshot

2-(4-Methoxyphenyl)-4H-1,3,2-benzoxathiaphosphinine 2-sulfide

inferred← citeshttps://doi.org/10.1134/s0012500817110015openalex-snapshot

Synthesis, crystal and molecular structure of 3,7-ditosyl-1,5-diphenyl-3,7-diazabicyclo[3.3.1]nonane

inferred← citeshttps://doi.org/10.1134/s1070428010050027openalex-snapshot

Regio- and stereoselective addition of methane- and bromomethanesulfonyl bromides to 1-phenylthiotricyclo[4.1.0.02,7]heptane

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Crystallographic study and molecular modeling on the oxidation product of N-[(8R)-2-methoxy-5,6,7,8,9,10-hexahydro-6,9-methanocyclohepta[b]indol-8-yl]acetamide

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Molecular modeling, X-ray diffraction analysis, and the study of iNOS inhibitor activity of 3-imino-2,4-diazabicyclo[3.3.1]nonan-1-ol hydrochloride

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Molecular and crystal structure of azabicyclo[3.3.1]nonane annelated with methylindole

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Structure and Absolute Configuration of the 11-Noriridoid “Chapingolide”

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СИНТЕЗ, КРИСТАЛЛИЧЕСКАЯ И МОЛЕКУЛЯРНАЯ СТРУКТУРА 3,7-ДИТОЗИЛ-1,5-ДИФЕНИЛ-3,7-ДИАЗАБИЦИКЛО[3.3.1]НОНАНА, "Доклады Академии наук"

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