anthracene undergoes diels alder reaction


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PDF Diels–Alder reactions and electrophilic substitutions with

Being an easily available conjugated -electron-rich carbocyclic π system anthracene (1a) has been widely exploited as a classic diene in Diels–Alder reactions wherein its chemical

  • What is a thermal Diels Alder reaction of anthracene?

    Other thermal Diels–Alder reactions of anthracene with alkenes attached to a heteroatom or halogen include those with tetrachloroethylene, 64 1,3-diacetylimidazolin-2-one, 65 alkenylimmonium salts, 66 vinyl- and propenyl-phosphines and ethyndiylbis (diphenylphosphine oxide) either by heating at reflux in a solvent or by heating in a sealed tube. 67

  • Is anthracene a classic diene?

    Being an easily available conjugated -electron-rich carbocyclic π system, anthracene (1a) has been widely exploited as a classic diene in Diels–Alder reactions wherein its chemical reactivity and transformational effectiveness are subsidized by the partial loss of aromaticity.

  • How do anthracenes react?

    A mechanistic rationale is offered with the aid of detailed computational studies, and finally, synthetic applications are presented. Anthracenes typically undergo Diels-Alder reactions or electrophilic substitutions at the central ring, but can be biased towards reacting at the terminal ring by appropriate blocking groups at the 9,10-positions.

  • What types of dienophiles are used in Diels Alder reactions?

    Additions to anthracene The types of dienophile used in the Diels–Alder reactions of anthracene fall broadly into four classes, namely (i) α,β-unsaturated carbonyls, (ii) alkenes attached to a heteroatom or halogen, (iii) alkenes and alkynes and (iv) hetero-dienophiles.

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