摘要
Reaction of a novel chiral N-acryloylhydrazide with various nitrile oxides proceeded smoothly to afford the cycloadduct with high diastereoselectivity (99:1). The auxiliary can be easily removed from the cycloadducts under mild conditions. (C) 2000 Elsevier Science Ltd.
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 1453-1456 |
| 頁數 | 4 |
| 期刊 | Tetrahedron Letters |
| 卷 | 41 |
| 發行號 | 9 |
| DOIs | |
| 出版狀態 | 已發佈 - 2000 2月 26 |
ASJC Scopus subject areas
- 生物化學
- 藥物發現
- 有機化學
指紋
深入研究「Diastereoselective [3+2] cycloadditions of a camphor-derived chiral N- acryloylhydrazide with nitrile oxides: The preparation of optically pure δ2-isoxazolines」主題。共同形成了獨特的指紋。引用此
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