摘要
Catalytic enantioselective 1,2-diboration of 1,3-dienes followed by cascade allylborations with dicarbonyls provides rapid entry into carbocyclic reaction products. The stereochemical course of this reaction was studied along with its application in the synthesis of pumilaside aglycon.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 2501-2504 |
| 页数 | 4 |
| 期刊 | Journal of the American Chemical Society |
| 卷 | 135 |
| 期 | 7 |
| DOI | |
| 出版状态 | 已出版 - 20 2月 2013 |
| 已对外发布 | 是 |
学术指纹
探究 'A catalytic enantioselective tandem allylation strategy for rapid terpene construction: Application to the synthesis of pumilaside aglycon' 的科研主题。它们共同构成独一无二的学术指纹。引用此
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