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Synthesis of the 5,6-dihydroxymorpholin-3-one fragment of monanchocidin A
1Department of Chemistry, North Carolina State University , Raleigh, North Carolina 27695, United States.
Abstract:
Monanchocidin A is a recently isolated pentacyclic guanidinium alkaloid that contains an unusual highly oxidized morpholinone fragment. Herein we report a rapid synthesis of this heterocyclic scaffold and confirm its structure. The key reaction involves an acid promoted hemiketalization/hemiaminalization of an α-hydroxyamide and α-ketoaldehyde that proceeds with exclusive regioselectivity and high diastereoselectivity to form the natural scaffold in moderate to high yield.
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