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Kinetics, isotope rate effect, and mechanism of dehydrobromination of cis-1,2-dibromoethylene with triethylamine in dimethylformamide

https://doi.org/10.1021/ja01030a044
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inferred← citeshttps://doi.org/10.2139/ssrn.4766478openalex-extracted
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inferred← citeshttps://doi.org/10.1002/9780470171875.ch1openalex-snapshot
A Critical Evaluation of the Concept of Fluorine Hyperconjugation
inferred← citeshttps://doi.org/10.1002/9780470771280.ch9openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.19720840502openalex-snapshot
Der syn‐ und anti‐koplanare Ablauf bimolekularer olefin‐bildender Eliminierungen
inferred← citeshttps://doi.org/10.1002/anie.197202001openalex-snapshot
The syn and anti Steric Course in Bimolecular Olefin‐Forming Eliminations
inferred← citeshttps://doi.org/10.1002/poc.610071002openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/zfch.19700100903openalex-snapshot
Nucleophile Substitutionen nach dem Eliminierungs‐Additions‐Mechanismus
inferred← citeshttps://doi.org/10.1007/0-306-46856-5_4openalex-snapshot
Study and Description of Organic Reaction Mechanisms
inferred← citeshttps://doi.org/10.1007/3-540-52422-3_3openalex-snapshot
Through-bond modulation of reaction centers by remote substituents
inferred← citeshttps://doi.org/10.1007/978-1-4613-9795-3_4openalex-snapshot
Study and Description of Organic Reaction Mechanisms
inferred← citeshttps://doi.org/10.1007/978-1-4615-8882-5_4openalex-snapshot
Study and Description of Organic Reaction Mechanisms
inferred← citeshttps://doi.org/10.1007/978-1-4757-1143-1_4openalex-snapshot
Study and Description of Organic Reaction Mechanisms
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)98055-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(01)84964-9openalex-snapshot
Isotope effects for the base-promoted dehydrochlorination of DDT in protic solvents. Evidence for ElcB elimination.
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)88548-8openalex-snapshot
Heterosubstituted vinyl carbanions I. Kinetic acidity of di- and trisubstituted haloethylenes.
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)94086-9openalex-snapshot
A very slow ElcB elimination under extreme ElcB conditions
inferred← citeshttps://doi.org/10.1016/s0069-8040(08)70194-8openalex-snapshot
Chapter 3 Elimination Reactions
inferred← citeshttps://doi.org/10.1021/ar50038a005openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ar50106a003openalex-snapshot
Nucleophilic substitution at acetylenic carbon. The last holdout
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When is an intermediate not an intermediate? Enforced mechanisms of general acid-base, catalyzed, carbocation, carbanion, and ligand exchange reaction
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Alkylidenecarbenes, Alkylidenecarbenoids, and Competing Species: Which Is Responsible for Vinylic Nucleophilic Substitution, [1 + 2] Cycloadditions, 1,5-CH Insertions, and the Fritsch−Buttenberg−Wiechell Rearrangement?
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An experimental and DFT study of the reaction between dichloroethylene carbonate and triethylamine in dimethyl carbonate
inferred← citeshttps://doi.org/10.1039/d5py00199dopenalex-snapshot
Multifunctional dithiolane monomers for multi-scale, recyclable light-driven additive manufacturing
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