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Deantiaromatization as a driving force in an electrocyclization of cyclopentadienone and the total synthesis of 1-epi-esco-pseudopteroxazole
(University of Missouri--Columbia, 2007)
Deantiaromatization has been successfully demonstrated as a driving force in an electrocyclization of cyclopentadienones. The reaction was found to be general for a number of substrates and provides a unique way to access ...
Diels-alder reactions of a cyclopentadienone derivative
(University of Missouri--Columbia, 2007)
An ester derivative of cyclopentadienone, a very reactive species, was generated from methyl-2-bromo-3-oxocyclopent-1-enecarboxylate (96) which dimerized instantaneously and decarbonylated to generate an indanone (97). ...
Studies on the nucleophilic substitution reactions of a dimeric cyclopentadienone
(University of Missouri--Columbia, 2007)
[ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Nucleophilic substitution reactions of 3,5-Dibromo-3a,4,7,7a-tetrahydro-4,7-methano-indene-1,8-dione (48) have been studied. Amines, thiols and alcohols ...