期刊
ORGANIC LETTERS
卷 11, 期 3, 页码 587-588出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol802635a
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资金
- University of Oslo
Starting from the ethyl ester of eicosapentaenoic acid, the first total synthesis of the marine natural product all-(Z)-5,7-dihydroxy-2(4Z, 7Z,10Z,13Z,16Z-nonadecapentaenyl)chromone has been achieved in six steps and in 14% overall yield.
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