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Asymmetric Diels-Alder reaction is one step in the biosynthesis of the statin lovastatin. [60] The retro-Diels–Alder reaction is used in the industrial production of cyclopentadiene. Cyclopentadiene is a precursor to various norbornenes, which are common monomers. The Diels–Alder reaction is also employed in the production of vitamin B6.
Printable version ; Page information; Get shortened URL ... Chemical diagram for showing a Diels-Alder reaction between anthracene and ... Anthracene Category:Singlet ...
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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
As such, the molecule is highly electrophilic, and is widely employed as a dienophile in cycloaddition reactions, such as the Diels-Alder reaction. It is also a potent Michael acceptor. [1] [2] This compound exists as a colorless liquid at room temperature. This compound was used in the preparation of nedocromil.
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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.