Reaction of allylsilanes and monothioacetals in the presence of Lewis acids: regioselectivity in the cleavage of the acetals
- 1 January 1982
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 8,p. 459-460
- https://doi.org/10.1039/c39820000459
Abstract
Trimethylallylsilane reacts with monothioacetals in the presence of tin (IV) chloride, titanium tetrachloride, or boron trifluoride–diethyl ether to give the homoallyl ethers and homoallyl sulphides.Keywords
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