Nucleophilic substitution at silicon: Evidence for electronic factors as driving force of the stereochemistry
- 10 January 1978
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 144 (2) , 165-173
- https://doi.org/10.1016/s0022-328x(00)84159-5
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Mechanism of nucleophilic substitution at silicon: kinetic evidence on the slow formation of a pentacoordinate silicon intermediateJournal of Organometallic Chemistry, 1975
- Regioselectivite dans la reduction par les hydrures: cyclopentenone - cyclohexenoneTetrahedron Letters, 1974
- The mechanism of nucleophilic substitution at silicon. Action of organometallic reagents on chiral bifunctional silanesJournal of Organometallic Chemistry, 1974
- Additions nucleophiles d′especes a charge localisee sur des cetones cycliques et des α-enones: Stereo et regioselectivites compareesTetrahedron Letters, 1974
- Regioselectivite et controle frontalier : Application a l'addition d'un anion phosphonate a la benzylidene acetoneTetrahedron Letters, 1973
- Stéréochimie des réactions de réactifs de grignard au niveau de l'atome de silicium d'un cyclosilane asymétriqueJournal of Organometallic Chemistry, 1972
- Reduction 1,2 ou 1,4 de carbonyles conjugues par les hydrures. Une tentative d'explication.Tetrahedron Letters, 1972
- Stéréochimie des réactions d'organolithiens et organosodiques au niveau de l'atome de silicium d'un cyclosilane asymétriqueJournal of Organometallic Chemistry, 1972
- Chemical reactivity and the concept of charge- and frontier-controlled reactionsJournal of the American Chemical Society, 1968
- Stereochemistry of Asymmetric Silicon. IV. The Sn2-Si Stereochemistry Rule for Good Leaving GroupsJournal of the American Chemical Society, 1967