Stereoelectronic effects in conformations of sulfide, sulfoxide, and sulfone α-carbanions
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- Type
- article
- Published
- 2015-12-02
- Cited by
- 7
- References
- 72
- OpenAlex
- https://openalex.org/W1938936214
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:93515161
Keywords
Carbanion, Sulfone, Chemistry, Sulfoxide, Conformational isomerism
References
- Sulphones in organic synthesis
- Sulfur reagents in organic synthesis
- Dependence of Stereoelectronic and Charge Effects on pKa Values of 1,3‐Dithiane‐Derived Sulfides, Sulfoxides, and Sulfones: An Experimental and Computational Investigation
- A Chemist's Guide to Density Functional Theory
- Structure-stability relationships in unsaturated sulfur compounds
- The Chemistry of C2‐Symmetric Bis(sulfoxides): A New Approach in Asymmetric Synthesis
- A Nonempirical Quantum-Chemical Study and Natural Bond Orbital Analysis of C6H5XCY3 Species (X = SO or SO2, Y = H or F)
- Conformationally Constrained Oxides of 1,3‐Dithiane: Synthesis and NMR Spectroscopic Investigations
- Conformationally constrained 2-methylidene 1,3-oxathiane S-oxides: synthesis and nucleophilic additions
- Benchmark calculations with correlated molecular wave functions. IV. The classical barrier height of the H+H2→H2+H reaction
- Ramberg–Bäckland reaction of α-chloromethyl methyl sulfone: A DFT study
- Conformational and stereoelectronic investigation of chloromethyl methyl sulfide and its sulfinyl and sulfonyl analogs
- Influence of resonance on the acidity of sulfides, sulfoxides, sulfones, and their group 16 congeners.
- Convincing evidence that the alkylation stereochemistry of cyclic α-lithio sulfoxides is governed by their chelated structure
- Enolate addition to a 2-alkylidene[1,3]dithiane-derived bissulfoxide. A new a(2)-acceptor.
- Electron affinities of the first‐row atoms revisited. Systematic basis sets and wave functions
- Organosulfur chemistry. II. Highly stereoselective reactions of 1,3-dithianes. Contrathermodynamic formation of unstable diastereoisomers
- Lithiated γ-O-functionalized propyl phenyl sulfides and sulfones of the type Li[CH(SOxPh)CH2CH2OR] (x = 0, 2). [LiCH(SPh)CH2CH2Ot-Bu(tmeda)] – A structurally characterized organolithium inner complex
- The structures of some sulphur-stabilized carbanions and stereoelectronic requirements for the formation of α-sulphonyl carbanions
- AB Initio Calculations on Sulfonylmethyl Anions
Cited by
- 1H, 13C NMR and ESI–MS studies of 1:1 complexes of some sulfenyl carbon acids with 1,5,7-triazabicyclo[4.4.0]dec-5-ene in solution
- Synthesis and acidity of conformationally constrained 1,3-oxathiane S-oxides
- Stereoelectronic Effects: The γ-Gauche Effect in Sulfoxides.
- Stereoelectronic Effects: Perlin Effects in Thiane‐Derived Compounds
- DFT Study and NBO Analysis of Conformation Properties of 2,5,5-Trimethyl-1,3,2-Dioxaphosphinane 2-Selenide and Their Dithia and Diselena Analogous
- Development of a Robust Protocol for the Determination of Weak Acids' pKa Values in DMSO.
- Stereoelectronic effects: Perlin effects in cyclohexane‐derived compounds
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- [H2-antihistaminics, III: Synthesis and H2-antihistaminic activity of sulfoxides and sulfones analogous to metiamide (author's transl)].
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