Regio- and stereo-selectivity in the silylation of 2,6-diethyl-3,4,7,8-tetramethyl-1,5-dihydro-s-indacene
Abstract
Disilylation of 2,6-diethyl-3,4,7,8-tetramethyl-1,5-dihydro-s-indacene is regioselective and stereoselective. The stereoselectivity was modified by changing the experimental conditions, allowing an understanding of the reaction mechanism. The structure of the 'meso' diastereoisomer was established by X-ray diffraction. Copyright © 2006 John Wiley & Sons, Ltd.
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Título según WOS: | Regio- and stereo-selectivity in the silylation of 2,6-diethyl-3,4,7,8-tetramethyl-1,5-dihydro-s-indacene |
Título según SCOPUS: | Regio- and stereo-selectivity in the silylation of 2,6-diethyl-3,4,7,8- tetramethyl-1,5-dihydro-s-indacene |
Título de la Revista: | APPLIED ORGANOMETALLIC CHEMISTRY |
Volumen: | 21 |
Número: | 1 |
Editorial: | Wiley |
Fecha de publicación: | 2007 |
Página de inicio: | 31 |
Página final: | 38 |
Idioma: | English |
URL: | http://doi.wiley.com/10.1002/aoc.1154 |
DOI: |
10.1002/aoc.1154 |
Notas: | ISI, SCOPUS |