摘要
We report the first example of highly enantioselective organocatalytic synthesis of 3-difluoroalkyl substituted 3-hydroxyoxindoles. The total synthesis of the difluoro analogue of convolutamydine E was achieved by this method.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 1919-1921 |
| 页数 | 3 |
| 期刊 | Chemical Communications |
| 卷 | 48 |
| 期 | 13 |
| DOI | |
| 出版状态 | 已出版 - 16 1月 2012 |
指纹
探究 'Organocatalytic asymmetric synthesis of 3-difluoroalkyl 3-hydroxyoxindoles' 的科研主题。它们共同构成独一无二的指纹。引用此
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