Reactivity of Bromodilithiosilane to Naphthalene and Anthracene
Bromodilithiosilane, 1, reacted with naphthalene at 110 °C to give the silacyclopropane derivative 2, which reacted with MeOH(D), MeI, and Me3SiCl to yield 3, 4, and 5 in 84%, 82%, and 85% yields, respectively. 1 also reacted with anthracene at −30 °C to give the lithio-silanorbornadiene derivatives...
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Veröffentlicht in: | Organometallics 2008-12, Vol.27 (23), p.6375-6378 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Bromodilithiosilane, 1, reacted with naphthalene at 110 °C to give the silacyclopropane derivative 2, which reacted with MeOH(D), MeI, and Me3SiCl to yield 3, 4, and 5 in 84%, 82%, and 85% yields, respectively. 1 also reacted with anthracene at −30 °C to give the lithio-silanorbornadiene derivatives, which were trapped by i-PrOH to yield 6 and 7 as colorless crystals in 27% and 54%. These results show an important synthetic application of a 1,1-dilithiosilane bearing a halogen atom, which differs from those of known 1,1-dilithiosilanes. |
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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/om800596t |