[PDF] The Diels-Alder Reaction of Anthracene with Maleic Anhydride
The Diels-Alder reaction is a member of a class of reactions called cycloadditions The reaction involves three π bonds, two from the diene and one from the dienophile in a concerted reaction to form a six-membered ring Anthracene acts as the diene and maleic anhydride functions as the dienophile
[PDF] Diels-Alder reaction between naphthalene and N-phenylmaleimide
12 The rate of the Diels-Alder reaction between substituted anthracenes and activated dienophile (7) increases by 5•104 times 13 It follows from these data that the
[PDF] Stereoelectronic effects in the Stereoselectivity of the Diels-Alder
The characteristic feature of anthracene behaving as a diene and its ability to undergo Diels-Alder reaction with various dienophiles have been well documented
DIELS-ALDER REACTION
we have chosen to include related aspects of the Diels-Alder reaction whenever they Substituted butadienes also undergo addition with maleic anhydride Isoprene product with a partially hydrogenated phenanthrene nucleus 33
[PDF] Experiment 20 — Pericyclic reactions
Pre-lab preparation (1) Read text section 22 6 (2) Write the potential Diels-Alder reactions of maleic anhydride and anthracene, and (3) estimate the reaction
[PDF] Abdel Al-Saeedipmd - Oriental Journal of Chemistry
of the Diels-Alder reaction of 9-substituted anthracene with a variety of dienophiles Key words: the ability to undergo cycloaddition reactions with a variety of
[PDF] High stereoselectivity in the Diels-Alder reaction of - NOPR
1-Succinimidoanthracene undergoes Diels-Alder reaction with maleic anhydride to give mainly the anti anthracene 1 with the unsymmetrical dienophile 2
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