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- Q267374 subject Q7458901.
- Q267374 subject Q8343673.
- Q267374 subject Q8983024.
- Q267374 abstract "The Prins reaction is an organic reaction consisting of an electrophilic addition of an aldehyde or ketone to an alkene or alkyne followed by capture of a nucleophile. The outcome of the reaction depends on reaction conditions (scheme 1). With water and a protic acid such as sulfuric acid as the reaction medium and formaldehyde the reaction product is a 1,3-diol. When water is absent, the cationic intermediate loses a proton to give an allylic alcohol. With an excess of formaldehyde and a low reaction temperature the reaction product is a dioxane. When water is replaced by acetic acid the corresponding esters are formed.".
- Q267374 thumbnail ThePrinsReaction.png?width=300.
- Q267374 wikiPageExternalLink Chapter26a.pdf.
- Q267374 wikiPageExternalLink prins-reaction.shtm.
- Q267374 wikiPageWikiLink Q101487.
- Q267374 wikiPageWikiLink Q101497.
- Q267374 wikiPageWikiLink Q104116.
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- Q267374 wikiPageWikiLink Q132187.
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- Q267374 wikiPageWikiLink Q7458901.
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- Q267374 wikiPageWikiLink Q8343673.
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- Q267374 comment "The Prins reaction is an organic reaction consisting of an electrophilic addition of an aldehyde or ketone to an alkene or alkyne followed by capture of a nucleophile. The outcome of the reaction depends on reaction conditions (scheme 1). With water and a protic acid such as sulfuric acid as the reaction medium and formaldehyde the reaction product is a 1,3-diol. When water is absent, the cationic intermediate loses a proton to give an allylic alcohol.".
- Q267374 label "Prins reaction".
- Q267374 depiction ThePrinsReaction.png.