Regio- and stereo-selectivities in some nucleophilic reactions
Top Cited Papers
- 6 March 2006
- book chapter
- Published by Springer Nature
- p. 145-162
- https://doi.org/10.1007/bfb0048506
Abstract
No abstract availableThis publication has 38 references indexed in Scilit:
- Simple prediction of cycloaddition orientation I—diels-alder reactionsTetrahedron, 1977
- Mechanism of nucleophilic substitution at silicon: kinetic evidence on the slow formation of a pentacoordinate silicon intermediateJournal of Organometallic Chemistry, 1975
- Sind Zwischenstufen mit pentakoordinierten C‐Atomen bei aliphatischen SN2‐Reaktionen nachgewiesen??Helvetica Chimica Acta, 1975
- The mechanism of nucleophilic substitution at silicon. Action of organometallic reagents on chiral bifunctional silanesJournal of Organometallic Chemistry, 1974
- Reactions of nucleophiles with ethylenic substratesAccounts of Chemical Research, 1971
- Organic quantum chemistry. XXIV. Theoretical study of the stereochemistry of SE2 and SN2 reactionsJournal of the American Chemical Society, 1970
- Hard and soft acids and bases, HSAB, part 1: Fundamental principlesJournal of Chemical Education, 1968
- Chemical reactivity and the concept of charge- and frontier-controlled reactionsJournal of the American Chemical Society, 1968
- Stereochemistry of Asymmetric Silicon. V. Coupling Reactions with Organometallic Reagents and Displacements of Chloride and Fluoride Leaving GroupsJournal of the American Chemical Society, 1967
- Addition Reactions of Organometallic Compounds with Conjugated Systems1Journal of the American Chemical Society, 1941