期刊
ORGANIC LETTERS
卷 19, 期 3, 页码 636-637出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b03793
关键词
-
资金
- Australian Research Council
An extremely concise total synthesis of a potent phosphodiesterase-4 inhibitory natural product, selaginpulvilin D, is reported. The synthesis features a one-pot, 3-fold electrophilic aromatic substitution sequence to assemble a 9,9-diaryilluorene core. The approach allows access to useful quantities of a selaginpulvilin natural product for the first time.
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