
Journal of Organic Chemistry p. 5544 - 5553 (1991)
Update date:2022-08-04
Topics:
Snider, Barry B.
Merritt, John E.
Dombroski, Mark A.
Buckman, Brad O.
Ethanol complements the typical solvent, acetic acid, for Mn(III)-based oxidative free-radical cyclizations.Cyclization of enol ether 1c to give gibberellic acid intermediate 6c is successfull in ethanol, but not in acetic acid.Ethanol acts as a reducing
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