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2. Furfuryl alcohol - Wikipedia

   en.wikipedia.org/wiki/Furfuryl_alcohol

   Hydrogenation of furfuryl alcohol can proceed to give hydroxymethyl derivative of tetrahydrofuran and 1,5-pentanediol. The etherification reaction of furfuryl alcohol with alkyl or aryl halide (e.g. benzyl chloride) in the liquid-liquid-liquid triphase system with the help of a phase transfer catalyst also reported. [ 7 ]

3. Methyl vinyl ketone - Wikipedia

   en.wikipedia.org/wiki/Methyl_vinyl_ketone

   Methyl vinyl ketone (MVK, IUPAC name: butenone) is the organic compound with the formula CH 3 C(O)CH=CH 2. It is a reactive compound classified as an enone , in fact the simplest example thereof. It is a colorless, flammable, highly toxic liquid with a pungent odor.

4. Furfurylamine - Wikipedia

   en.wikipedia.org/wiki/Furfurylamine

   [1] The pharmaceutical drug furtrethonium , a parasympathomimetic cholinergic , is a trimethyl ammonium derivative of furfurylamine. Furfurylamine also has use in the synthesis of Barmastine .

5. Furfural - Wikipedia

   en.wikipedia.org/wiki/Furfural

   Furfural is an organic compound with the formula C 4 H 3 OCHO. It is a colorless liquid, although commercial samples are often brown. It has an aldehyde group attached to the 2-position of furan. It is a product of the dehydration of sugars, as occurs in a variety of agricultural byproducts, including corncobs, oat, wheat bran, and sawdust.

6. Furan-2-ylmethanethiol - Wikipedia

   en.wikipedia.org/wiki/Furan-2-ylmethanethiol

   Furan-2-ylmethanethiol (2-furanmethanethiol) is an organic compound containing a furan substituted with a sulfanylmethyl group. It is a clear colourless liquid when ...

7. Furil - Wikipedia

   en.wikipedia.org/wiki/Furil

   Furil, also commonly known as α-furil or 2,2′-furil, is a furan compound. References. Material Safety Data Sheet; Chemexper.com

8. Allylic rearrangement - Wikipedia

   en.wikipedia.org/wiki/Allylic_rearrangement

   In the similar substitution of 1-chloro-3-methyl-2-butene, the secondary 2-methyl-3-buten-2-ol is produced in a yield of 85%, while that for the primary 3-methyl-2-buten-1-ol is 15%. Allylic shifts occur because the transition state is an allyl intermediate. In other respects they are similar to classical nucleophilic substitution, and admit ...

9. Category:3-Furyl compounds - Wikipedia

   en.wikipedia.org/wiki/Category:3-Furyl_compounds

   This page was last edited on 28 October 2022, at 14:36 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.