[3,3]-Sigmatropic rearrangement of silyl ketene acetals of methyl α-(allyloxy) acetates.
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (14) , 1557-1560
- https://doi.org/10.1016/s0040-4039(00)84311-7
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- The anionic oxy-claisen rearrangement of enolates of .alpha.-allyloxy ketones. A remarkable rate accelerating effect exhibited by the nature of the counterionJournal of the American Chemical Society, 1985
- Catalysis of the Cope and Claisen rearrangementsChemical Reviews, 1984
- The [2,3]Wittig rearrangement of 2-alkenyloxyacetic acids and its applications to the stereocontrolled synthesis of β, γ-unsaturated aldehydes and conjugated dienoic acidsTetrahedron Letters, 1981
- Allyloxy ketone enol ether-claisen rearrangement. regiospecific synthesis of allyl ketones from allyl alcoholsTetrahedron Letters, 1977
- Stereo- and regiochemistry of the Claisen rearrangement: applications to natural products synthesisAccounts of Chemical Research, 1977
- The Claisen Rearrangement in Organic Synthesis; 1967 to January 1977Synthesis, 1977
- The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formationJournal of the American Chemical Society, 1976
- The [2,3] Sigmatropic Reaction of Acetonyl Allyl Ethers, a new method for preparing certain 2‐hydroxyketonesHelvetica Chimica Acta, 1974
- Claisen rearrangement of allyl estersJournal of the American Chemical Society, 1972