Journal
ORGANIC LETTERS
Volume 6, Issue 11, Pages 1749-1752Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol0495772
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- NIGMS NIH HHS [GM 54656] Funding Source: Medline
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Enantioselective synthesis of (+)-ricciocarpins A and B has been achieved in 41 and 45% overall yields, respectively, starting from a beta-substituted oxazolidinone. The key steps in the strategy are an enantioselective conjugate radical addition and the addition of a furyl organometallic to a key aldehyde intermediate.
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