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Propanolysis of arenesulfonyl chlorides: Nucleophilic substitution at sulfonyl sulfur
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/3527601791openalex-snapshot
Solvents and Solvent Effects in Organic Chemistry
inferredcites →https://doi.org/10.1002/jcc.23607openalex-snapshot
SN1‐SN2 and SN2‐SN3 mechanistic changes revealed by transition states of the hydrolyses of benzyl chlorides and benzenesulfonyl chlorides
inferredcites →https://doi.org/10.1002/jps.2600690938openalex-snapshot
Substituent Constants for Correlation Analysis in Chemistry and Biology.
inferredcites →https://doi.org/10.1002/kin.20945openalex-snapshot
Isotope Effects in the Solvolysis of Sterically Hindered Arenesulfonyl Chlorides
inferredcites →https://doi.org/10.1002/poc.1262openalex-snapshot
Substituent effects on the formation of sulfonyl cations from sulfonyl chlorides: comparisons of solvolysis kinetic data with calculated gas phase energies
inferredcites →https://doi.org/10.1002/poc.1522openalex-snapshot
The SN3–SN2 spectrum. Rate constants and product selectivities for solvolyses of benzenesulfonyl chlorides in aqueous alcohols
inferredcites →https://doi.org/10.1002/poc.3585openalex-snapshot
Positioning solvolyses within the SN2‐SN1 and SN3‐SN2 spectrum of reaction mechanisms
inferredcites →https://doi.org/10.1016/s0020-1693(00)83080-7openalex-snapshot
Chemical kinetics: The study of reaction rates in solution
inferredcites →https://doi.org/10.1016/s0040-4039(00)72131-9openalex-snapshot
Chlorine isotopic exchange at sulphur in sulphonyl chlorides. Accelerating effect of the ortho-alkyl groups
inferredcites →https://doi.org/10.1021/ci000089sopenalex-snapshot
A Program for Linear Regression with a Common Point of Intersection: The Isokinetic Relationship
inferredcites →https://doi.org/10.1021/cr990416zopenalex-snapshot
Isokinetic Relationship, Isoequilibrium Relationship, and Enthalpy−Entropy Compensation
inferredcites →https://doi.org/10.1021/ja00757a041openalex-snapshot
Hydrolysis of sulfamoyl chlorides. I. Hydrolysis of dimethylsulfamoyl chloride. Heat capacity of activation, the secondary .gamma.-deuterium isotope effect, and solvent isotope effect
inferredcites →https://doi.org/10.1021/ja00839a047openalex-snapshot
Steric effects. I. Esterification and acid-catalyzed hydrolysis of esters
inferredcites →https://doi.org/10.1021/ja01588a048openalex-snapshot
Kinetics of Reactions of Acyl Chlorides. II. Mechanisms of Hydrolysis of Sulfonyl Chlorides
inferredcites →https://doi.org/10.1021/jp206665wopenalex-snapshot
Hydrogen Bonding and Molecular Aggregates in Liquid Methanol, Ethanol, and 1-Propanol
inferredcites →https://doi.org/10.1021/jp9928558openalex-snapshot
Hydrogen Bonding in 2-Propanol. The Effect of Fluorination
inferredcites →https://doi.org/10.1021/ol1029113openalex-snapshot
The Hydrolysis of 4-Amino- and 4-Dimethylaminobenzene Sulfonyl Chlorides: An Unprecedented Case of Independence of Reactivity from pH
inferredcites →https://doi.org/10.1039/a802786bopenalex-snapshot
Concentrated salt effects on the rates of solvolyses involving carbocations as reaction intermediates in acetone–water mixed solvents
inferredcites →https://doi.org/10.1039/b518129aopenalex-snapshot
Rate and product studies in the solvolyses of N,N-dimethylsulfamoyl and 2-propanesulfonyl chlorides
inferredcites →https://doi.org/10.1039/c39910000854openalex-snapshot
Sulphonyl transfer reactions: solvolysis of arenesulphonyl chlorides in aqueous trifluoroethanol
inferredcites →https://doi.org/10.1039/j29680000157openalex-snapshot
The separation of polar and steric effects. Part VI. The kinetics of the acid-catalysed esterification of substituted benzoic acids by methanol
inferredcites →https://doi.org/10.1039/p29720000468openalex-snapshot
Nucleophilic substitution at four-co-ordinate sulphur. Mobility of the leaving group
inferredcites →https://doi.org/10.1039/p29740000722openalex-snapshot
Neutral and alkaline hydrolysis of 2,4,6-trimethylbenzenesulphonyl chloride
inferredcites →https://doi.org/10.1039/p29750000637openalex-snapshot
Reactions of organic sulphur compounds. Part I. The hydrolysis of arenesulphonyl chlorides
inferredcites →https://doi.org/10.1039/p29810000438openalex-snapshot
Nucleophilic substitution at sulphonyl sulphur. Part 2. Hydrolysis and alcoholysis of aromatic sulphonyl chlorides
inferredcites →https://doi.org/10.1039/p29880001793openalex-snapshot
Nucleophilic substitution at sulphonyl sulphur. Part 4. Hydrolysis of substituted thiophenesulphonyl halides in water–acetone mixtures
inferredcites →https://doi.org/10.1039/p29910000175openalex-snapshot
Limitations of the transition state variation model. Part 2. Dual reaction channels for solvolyses of 2,4,6-trimethylbenzenesulphonyl chloride
inferredcites →https://doi.org/10.1039/p29910001175openalex-snapshot
Limitations of the transition-state variation model. Part 3. Solvolyses of electron-rich benzenesulphonyl chlorides
inferredcites →https://doi.org/10.1071/ch9610190openalex-snapshot
Solvolysis of Sulphonyl Halides. I. The Hydrolysis of Aromatic Sulphonyl Chlorides in Aqueous Dioxan and Aqueous Acetone
inferredcites →https://doi.org/10.1071/ch9610205openalex-snapshot
Solvolysis of Sulphonyl Halides. II. The Alcoholysis of Aromatic Sulphonyl Chlorides in Ethanol-Acetone and Methanol-Acetone
inferredcites →https://doi.org/10.1071/ch9710703openalex-snapshot
Solvolysis of sulphonyl halides. VII. Hydrolysis of some aromatic sulphonyl chlorides in aqueous dioxan
inferredcites →https://doi.org/10.1139/v71-236openalex-snapshot
Sulfonyl Chloride Kinetics. Part II. Solvolysis of a Series of Benzenesulfonyl Chlorides: An Unexpected Heat Capacity Variation
inferredcites →https://doi.org/10.1139/v71-237openalex-snapshot
Sulfonyl Chloride Kinetics. Part III. Nucleophilic Interaction on the Transition State for 4-X-Benzenesulfonyl Chloride Solvolyses
inferredcites →https://doi.org/10.1590/s0100-40421997000300003openalex-snapshot
Reatividade Relativa em Solvólise Nucleofílica de Cloretos de Arilsulfenila, Arilcarbonila, Arilsulfonila, Arilmetila e de Arila
inferredcites →https://doi.org/10.30970/vchopenalex-snapshot
Visnyk of the Lviv University. Series Chemistry
inferredcites →https://doi.org/10.3184/030823408x293189openalex-snapshot
Sixty Years of the Grunwald–Winstein Equation: Development and Recent Applications
inferredcites →https://doi.org/10.3390/ijms160510601openalex-snapshot
Calculated Third Order Rate Constants for Interpreting the Mechanisms of Hydrolyses of Chloroformates, Carboxylic Acid Halides, Sulfonyl Chlorides and Phosphorochloridates
inferredcites →https://doi.org/10.3390/ijms9122639openalex-snapshot
Correlation of the Rates of Solvolysis of Two Arenesulfonyl Chlorides and of trans-β-Styrenesulfonyl Chloride — Precursors in the Development of New Pharmaceuticals
inferredcites →https://doi.org/10.5012/bkcs.2014.35.1.51openalex-snapshot
Product-Rate Correlations for Solvolyses of 2,4-Dimethoxybenzenesulfonyl Chloride
inferredcites →https://doi.org/10.5860/choice.40-3409openalex-snapshot
Chlorosulfonic acid: a versatile reagent
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.4782893openalex-extracted
Sulfonate-Bridged Semi-Biopolyamide for Pb(Ii) Electrochemical Probing and Dye Adsorption
inferred← citeshttps://doi.org/10.1002/9781118707838.ch2openalex-snapshot
Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and Their Derivatives
inferred← citeshttps://doi.org/10.1002/9781119531975.ch2openalex-snapshot
Reactions of Carboxylic, Phosphoric and Sulfonic Acids and their Derivatives
inferred← citeshttps://doi.org/10.1002/chem.70739openalex-snapshot
Stability of Heteroaromatic Sulfonyl Chlorides and Fluorides
inferred← citeshttps://doi.org/10.1002/ejoc.70600openalex-snapshot
Electrochemical Three‐Component Synthesis of Heteroaryl Sulfonates
inferred← citeshttps://doi.org/10.1007/s10853-022-06956-9openalex-snapshot
Effective strategy for improving electrical properties of polyethylene insulating materials by doping graphene
inferred← citeshttps://doi.org/10.1080/10601325.2024.2376539openalex-snapshot
Sulfonate-bridged semi-biopolyamide for Pb(II) electrochemical probing and dye adsorption
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