Lewis acid mediated reactions of 2-stannyl-3-silylpropene with acid chlorides. Formation of vinylsilanes via 1,2-silyl migration and destannylation.
- 1 August 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (34) , 4953-4956
- https://doi.org/10.1016/s0040-4039(00)61243-1
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- [2 + 1] Cycloaddition of (E)-1-(phenylseleno)-2-(trimethylsilyl)ethene. Novel cyclopropane ring formation by a 1,2-shift of a trimethylsilyl groupThe Journal of Organic Chemistry, 1992
- Synthesis of functionalized allylsilanes via palladium-catalyzed cross-coupling of 2-stannyl-3-silylpropene with organic halides.Tetrahedron Letters, 1991
- A new synthesis of substituted furansJournal of the American Chemical Society, 1989
- The influence of (organo)metallics “metal-tuning” on stereo- and regio-chemical convergence in reactions of allylic carbanions with aldehydesJournal of Organometallic Chemistry, 1985
- A mechanistic study of the acid- and base-catalysed cleavages of β-trimethylstannylstyrenesJournal of Organometallic Chemistry, 1980
- A short new azulene synthesisJournal of the American Chemical Society, 1980
- Allylic terpenyl silanes. Versatile synthons in the terpene series synthesis of 2-acyl-.DELTA.(1,7)-p-menthenes and 3-acyl-.beta.-pinenesThe Journal of Organic Chemistry, 1979