Direct substitution of secondary allylic alcohols with O-silylated ketene acetals in 3.0 M lithium perchlorate-diethyl ether - An alternative to the [1,3] sigmatropic rearrangement of allyl vinyl ethers
- 11 August 1992
- journal article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 33 (33), 4735-4738
- https://doi.org/10.1016/s0040-4039(00)61272-8
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Chelation controlled addition of allylstannanes to aldehydes in lithium perchlorate-diethyl etherTetrahedron Letters, 1992
- Lithium perchlorate catalyzed conjugate addition of o-silylated ketene acetals to hindered α,β-unsaturated carbonyl compounds at atmospheric pressureTetrahedron Letters, 1991
- [1,3]-Sigmatropic rearrangement of allyl vinyl ethers at ambient temperature in 3.0 M lithium, perchlorate-diethyl etherJournal of the American Chemical Society, 1991
- Dramatic rate accelerations of Diels-Alder reactions in 5 M lithium perchlorate-diethyl ether: the cantharidin problem reexaminedJournal of the American Chemical Society, 1990