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
Hauptverfasser: Lim, Young Mook, Lee, Myong Euy, Lee, Junseong, Do, Youngkyu
Format: Artikel
Sprache:eng
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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.
ISSN:0276-7333
1520-6041
DOI:10.1021/om800596t