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Reactions
4 reactions imported from Wikipedia named-reactions and Organic Syntheses archives. Filter by source or search by name + summary.
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| Equation | Name | Summary | Source |
|---|---|---|---|
| ALKYNES via PHASE TRANSFER–CATALYZED DEHYDROHALOGENATION: PROPIOLALDEHYDE DIETHYL ACETAL (1-Propyne, 3,3-diethoxy-) Halogenation | Preparation of 1-Propyne, 3,3-diethoxy-. Submitted by A. Le Coq1 and A. Gorgues. DOI: 10.15227/orgsyn.059.0010. | Organic Syntheses | |
| ALKYNE via SOLID-LIQUID PHASE-TRANSFER CATALYZED DEHYDROHALOGENATION: ACETYLENE DICARBOXALDEHYDE TETRAMETHYL ACETAL AND ACETYLENE DICARBOXALDEHYDE DIMETHYL ACETAL (1,1,4,4-Tetramethoxy-2-butyne and 4,4-Dimethoxy-2-Butynal) Halogenation | Preparation of 1,1,4,4-Tetramethoxy-2-butyne and 4,4-Dimethoxy-2-Butynal. Submitted by Rufine Akué-Gédu and Benoît Rigo1. DOI: 10.15227/orgsyn.082.0179. | Organic Syntheses | |
| Darzens halogenation Halogenation | Darzens halogenation is the chemical synthesis of alkyl halides from alcohols via the treatment upon reflux of a large excess of thionyl chloride or thionyl bromide (SOX2) in the presence of a small a… | Wikipedia: Category:Name reactions | |
| Hell–Volhard–Zelinsky halogenation Halogenation | The Hell–Volhard–Zelinsky halogenation reaction is a chemical transformation that transforms an alkyl carboxylic acid to the α-bromo derivative. It is a specialized and rare kind of halogenation. | Wikipedia: Category:Name reactions |
