The mechanism of nucleophilic substitution at silicon: solvent influence on the rates of organometallicorganosilane coupling reactions
- 1 May 1974
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 71 (3) , 393-397
- https://doi.org/10.1016/s0022-328x(00)95170-2
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- SNi-Si mechanism. Reductive displacement of good leaving groups with retention of configuration by diisobutylaluminum hydride. Stereochemical and mechanistic crossover with the etherate complex of diisobutylaluminum hydrideJournal of the American Chemical Society, 1972
- Solvent effects on the stereochemistry of coupling reactions of Grignard reagents with organosilanesJournal of the Chemical Society D: Chemical Communications, 1971
- Effets de solvants and du chlorure de lithium sur la stereochimie de reduction du s(−) methyl phenyl α-naphtyl menthoxy 3R germanium par LiAlH4.Tetrahedron Letters, 1970