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A novel enantioselective synthetic route to omuralide analogues with the potential for species selectivity in proteasome inhibition.

Crane SN, Corey EJ. A novel enantioselective synthetic route to omuralide analogues with the potential for species selectivity in proteasome inhibition. Org Lett. 2001 May 03; 3(9):1395-7.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.