J.D. Sellars
Hosomi-Sakurai reactions of silacyclic allyl silanes
Sellars, J.D.; Steel, P.G.; Turner, M.J.
Abstract
Substituted silacyclohexenes, generated through silene–diene [4 + 2] cycloaddition reactions, undergo Lewis acid promoted Sakurai type reactions with acetals to afford, following oxidation of the resultant fluorosilane, 1,4-diols with four contiguous chiral centres.
Citation
Sellars, J., Steel, P., & Turner, M. (2006). Hosomi-Sakurai reactions of silacyclic allyl silanes. Chemical Communications, 2385-2387. https://doi.org/10.1039/b602642g
| Journal Article Type | Article |
|---|---|
| Publication Date | May 1, 2006 |
| Deposit Date | May 4, 2007 |
| Journal | Chemical Communications |
| Print ISSN | 1359-7345 |
| Electronic ISSN | 1364-548X |
| Publisher | Royal Society of Chemistry |
| Peer Reviewed | Peer Reviewed |
| Issue | 22 |
| Pages | 2385-2387 |
| DOI | https://doi.org/10.1039/b602642g |
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