Hosomi-Sakurai reactions of silacyclic allyl silanes

Sellars, J.D.; Steel, P.G.; Turner, M.J.

doi:10.1039/b602642g

All Outputs (2)

Silenes in organic synthesis: a short synthesis of prelactone B (2006)
Journal Article
Sellars, J., & Steel, P. (2006). Silenes in organic synthesis: a short synthesis of prelactone B. Organic and Biomolecular Chemistry, 4(17), 3223-3224. https://doi.org/10.1039/b608989e

Hosomi-Sakurai reactions of silacyclic allyl silanes (2006)
Journal Article
Sellars, J., Steel, P., & Turner, M. (2006). Hosomi-Sakurai reactions of silacyclic allyl silanes. Chemical Communications, 2385-2387. https://doi.org/10.1039/b602642g

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... Read More about Hosomi-Sakurai reactions of silacyclic allyl silanes.