Thiiranium Ions as Reaction Intermediates
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- Type
- article
- Published
- 1969-07-01
- Cited by
- 66
- References
- 0
- OpenAlex
- https://openalex.org/W2070590414
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:96541208
Keywords
Steric effects, Electrophile, Ion, Ring (chemistry), Chemistry
References
Cited by
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- The production of episulfonium complexes from propylene and the regioselectivity of their reactions with nucleophiles
- A Fast and Efficient Route to 5-Chloromethyl-1,4,7,10-Tetrathiacyclotridecane and its Behavior in a Chloroform Solution
- Offene und verbrückte Zwischenstufen, 9. Regioselektive Synthesen von Vinylthioethern
- NEW ACTIVE SULFUR TRANSFER REAGENTS: ARENETHIOSULFENYL CHLORIDES. A CONVENIENT SYNTHESIS OF EPISULFIDES FROM OLEFINS
- Synthesis of fluoro-substituted acrylic monomers bearing a functionalized lateral chain
- The nucleophilic substitution of chlorine in derivatives of β -chloro- α -methylthioisovaleric acid
- 1,2-Migration of methyl group in reaction of tert-butylethylene with phenylsulfenyl fluoborate
- Studies on β-lactam antibiotics. I. A novel conversion of penicillins into cephalosporins
- Thiiranium and Thiirenium Ions Chemistry and Stereochemistry
- Synthese von Allylthioethern
- Isomerization of β-halo disulfides (alkyl 2-haloethyl disulfides)
- Aminosäuren, 14. Diastereoselektive Addition von Benzolsulfenylchlorid an 1-Acryloylprolinester
- Quantum chemical studies on electrophilic addition
- Generation and properties of episulfonium intermediates communication 5. Stereochemistry of formation and opening of episulfonium complexes obtained from cis- and trans-butenes
- TRIFLUOROMETHYLTHIOLATION OF NORBORNENE
- Novel generation of arylsulfenium ion intermediates and efficient aromatic arylthiolation by the intermediates
- The Addition of 2,4-Dinitrobenzenesulfenyl Chloride to cis- and trans-1-Arylpropenes and Some Other Olefins
- Umsetzungen von Chlordisulfanylameisensurechlorid mit Olefinen oder -Dicarbonylverbindungen
- Offene und verbrückte Zwischenstufen, 7. Zum Bildungsmechanismus von Allylprodukten bei elektrophilen Additionen an Olefine
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