3-Stannyl-1-silyloxycyclohex-1-enes: Synthetic equivalents for ketone α, β-dianions
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (25) , 2805-2808
- https://doi.org/10.1016/s0040-4039(00)84647-x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Silyl stannanes: useful reagents for bis-functionalization of .alpha.,.beta.-unsaturated ketones and acetylenesThe Journal of Organic Chemistry, 1985
- General method for generation of 3-siloxyallylmetallic species and their synthetic applicationJournal of the American Chemical Society, 1985
- Base-induced rearrangement of 1-(trimethylsilyl)allylic alcohols. Stereo- and regioselective synthesis of silyl enol ethers through lithium homoenolatesJournal of the American Chemical Society, 1984
- Tris(dialkylamino)sulfonium enolates. Synthesis, structure, and reactionsJournal of the American Chemical Society, 1983
- Homoenolate anions and homoenolate anion equivalentsTetrahedron, 1983
- Erythro-selective aldol reaction via tris(dialkylamino)sulfonium enolatesJournal of the American Chemical Society, 1981
- .beta.-Acylvinyl anion equivalents: preparation of 1-lithio-3-(tert-butyldimethylsiloxy)-1,3-cyclohexadiene and its reaction with electrophilesThe Journal of Organic Chemistry, 1979
- Stannylation/destannylation. Preparation of .alpha.-alkoxy organolithium reagents and synthesis of dendrolasin via a carbinyl carbanion equivalentJournal of the American Chemical Society, 1978
- An expeditious route to the germacranes. Total synthesis of (.+-.)-acoragermacrone and (.+-.)-preisocalamendiolJournal of the American Chemical Society, 1977