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  2. Diels–Alder reaction - Wikipedia

    en.wikipedia.org/wiki/DielsAlder_reaction

    Asymmetric Diels-Alder reaction is one step in the biosynthesis of the statin lovastatin. [60] The retro-DielsAlder reaction is used in the industrial production of cyclopentadiene. Cyclopentadiene is a precursor to various norbornenes, which are common monomers. The DielsAlder reaction is also employed in the production of vitamin B6.

  3. File:2,3-dimethyl-1,3-butadiene Diels-Alder Reaction.svg

    en.wikipedia.org/wiki/File:2,3-dimethyl-1,3...

    This file contains additional information, probably added from the digital camera or scanner used to create or digitize it. If the file has been modified from its original state, some details may not fully reflect the modified file.

  4. File:Original Diels-Alder reaction.svg - Wikipedia

    en.wikipedia.org/wiki/File:Original_Diels-Alder...

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  5. File:Comparison between Diels-Alder and captodative-enhanced ...

    en.wikipedia.org/wiki/File:Comparison_between...

    English: Comparison between Diels-Alder reaction of cyclopentadiene with 2-methylthioacrylonitrile and captodative-enhanced Friedel-Crafts reaction of benzene with 1-nitrovinyl alcohol Date 11 October 2017

  6. File:Anthracene singlet oxygen Diels-Alder reaction.svg

    en.wikipedia.org/wiki/File:Anthracene_singlet...

    English: Chemical diagram for showing a Diels-Alder reaction between anthracene and singlet oxygen. Date: 17 June 2022: Source: Own work: Author: User:Innerstream ...

  7. Boger pyridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Boger_pyridine_synthesis

    The Boger pyridine synthesis is a cycloaddition approach to the formation of pyridines named after its inventor Dale L. Boger, who first reported it in 1981. [1] The reaction is a form of inverse-electron demand Diels-Alder reaction in which an enamine reacts with a 1,2,4-triazine to form the pyridine nucleus.

  8. Hexaphenylbenzene - Wikipedia

    en.wikipedia.org/wiki/Hexaphenylbenzene

    The reaction proceeds via a Diels-Alder reaction to give the hexaphenyldienone, which then eliminates carbon monoxide. [ 1 ] Together with 1,2,3,4-tetraphenylnaphthalene, hexaphenylbenzene forms by the chromium-catalyzed oligomerization of diphenylacetylene . [ 3 ]

  9. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    The Diels-Alder reaction, also known as cycloaddition, combines a conjugated diene and an alkene to form cycloalkene. This is a concerted process, with bonds forming and breaking simultaneously. This is a concerted process, with bonds forming and breaking simultaneously.