Solvent-Dependent Stereoselectivity in the Addition ofp-CH3OC6H4OH to (E)-1,2-Di-tert-butyl-1,2-dimesityldisilene. Evidence for Rotation around the Si−Si Bond in the Zwitterionic Intermediate
- 1 March 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Organometallics
- Vol. 17 (7) , 1260-1265
- https://doi.org/10.1021/om970700l
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Structure of the THF Solvate of TetramesityldisileneOrganometallics, 1996
- STEREOSELECTIVE ADDITION OF ALCOHOLS TO STABLE DISILENESMain Group Metal Chemistry, 1996
- The Mechanism of Addition of Phenols to Tetramesityldisilene. Evidence for Both Nucleophilic and Electrophilic Rate-Determining StepsJournal of the American Chemical Society, 1996
- The chemistry of organosilicon compounds. 302. Regio- and stereochemistry and kinetics in the addition reactions of alcohols to phenyl-substituted disilenesJournal of the American Chemical Society, 1993
- Phase annealing in SHELX-90: direct methods for larger structuresActa Crystallographica Section A Foundations of Crystallography, 1990
- Structural Chemistry of Organic Silicon CompoundsPublished by Wiley ,1989
- X-ray crystal structures for two disilenesOrganometallics, 1984
- Cis and trans isomers of disilenes: photochemical and thermal interconversionsJournal of the American Chemical Society, 1984
- Solvent Effects on Transition States and Reaction RatesPublished by Wiley ,1974
- Quantitative Comparisons of Weak Organic BasesPublished by Wiley ,1963