期刊论文详细信息
| TETRAHEDRON LETTERS | 卷:56 |
| Alkoxy-directed cyclopropanation of 1,1-disubstituted alkenes with esters: new approach to quaternary carbon centers | |
| Article | |
| Rao, Nagavaram Narsimha1  Cha, Jin Kun1  | |
| [1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA | |
| 关键词: Cyclopropanation; Cyclopropanol; Homoenol; Directing group; Quaternary center; | |
| DOI : 10.1016/j.tetlet.2014.12.043 | |
| 来源: Elsevier | |
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【 摘 要 】
As a new approach to the stereocontrolled construction of quaternary centers, 1,2,2-trisubstituted cyclopropanols are prepared by the olefin exchange-mediated Kulinkovich cyclopropanation of esters with 1,1-disubstituted alkenes bearing homoallylic alcohols. Central to the successful cyclopropanation is the generation of a temporary alkoxy tether from a homoallylic alcohol. (C) 2014 Elsevier Ltd. All rights reserved.
【 授权许可】
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【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 10_1016_j_tetlet_2014_12_043.pdf | 392KB |
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