Journal
ORGANIC LETTERS
Volume 2, Issue 15, Pages 2213-2215Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol005953g
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- NIGMS NIH HHS [GM58877] Funding Source: Medline
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[GRAPHICS] The enantiospecific and regioselective rhodium-catalyzed allylic alkylation of a series of chiral nonracemic allylic carbonates, followed by ozonolysis and reductive lactonization, provides a convenient route to optically active gamma-lactones, Sequential alkylation and reductive alkylation furnished the alpha-quaternary-beta-ternary substituted gamma-lactone derivative as a greater than or equal to 10:1 mixture of diastereoisomers.
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