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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