Substituent effects and the role of negative hyperconjugation in siloxycarbene rearrangements
Authors: Paul G Loncke
Affiliations
1 Centre for Research in Molecular Modeling, Concordia University, Montreal, Quebec, Canada H4B 1R6.
Description
Substituent effects and the role of negative hyperconjugation in 1,2-silyl migration and decarbonylation of methoxy(substituted-siloxy)carbenes have been investigated using quantum chemical calculations and natural bond orbital analysis. It has been found that sigma-electron-withdrawing substituents generally lower the barriers for 1,2-silyl migration and decarbonylation, consistent with symmetry-forbidden concerted rearrangements involving intramolecular front-side nucleophilic attack by the...
Links
PubMed: https://pubmed.ncbi.nlm.nih.gov/15917909/
DOI: 10.1039/b416058d