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Rapid and Enantioselective Assembly of the Lycorine Framework Using Chemoenzymatic Techniques

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Authors

Jones, Matthew
Schwartz, Brett
Willis, Anthony
Banwell, Martin

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American Chemical Society

Abstract

The pentacyclic framework associated with the alkaloid (-)-lycorine (1) can be assembled in as few as six steps from the enantiomerically pure cis-1,2-dihydrocatechol 3 which is itself readily available on a large scale through the whole-cell biotransformation of bromobenzene. The methodology has been used in developing the first synthesis of compound 2, a derivative of lycorine.

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Organic Letters

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Restricted until

2037-12-31
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