| 11. | An intramolecular Diels Alder reaction is carried out to form the macrocyclic ring.
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| 12. | Cycloalkanes can be formed in a Diels Alder reaction followed by a catalytic hydrogenation.
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| 13. | The endo product is generally favored, as in the isoelectronic Diels Alder reaction.
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| 14. | Himbacine has been synthesized using a Diels-Alder reaction as a key step.
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| 15. | It can be prepared by the Diels Alder reaction of dimethyl maleate and cyclopentadiene.
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| 16. | Tandem DKR-intramolecular Diels-Alder reaction.
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| 17. | Porphyrin trimer catalyst developed by Jeremy Sanders for exo selective Diels-Alder reactions.
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| 18. | This photoredox-catalyzed Diels Alder reaction allows cycloaddition between two electronically mismatched substrates.
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| 19. | In the first step the triazine reacts with the fullerene in a Diels-Alder reaction.
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| 20. | Diels-Alder reactions can lead to formation of a variety of structural isomers and stereoisomers.
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