Formation of tetrabenzodispiro[4.0.4.3]tridecatetraene by a titanium mediated fluorenyl coupling reaction
Treatment of 1,3-propanediol-ditosylate with fluorenyllithium yields 1,3-bis(fluorenyl)propane ( 5). Subsequent addition of methyl-lithium gives the corresponding dilithio compound 6. Dilithio-1,3-bis(fluorenyl)propane ( 6) was treated with titanium tetrachloride to yield the organic tetrabenzodispi...
Saved in:
Published in | Journal of organometallic chemistry Vol. 501; no. 1; pp. 41 - 45 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
LAUSANNE 1
Elsevier B.V
04.10.1995
Elsevier |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Treatment of 1,3-propanediol-ditosylate with fluorenyllithium yields 1,3-bis(fluorenyl)propane (
5). Subsequent addition of methyl-lithium gives the corresponding dilithio compound
6. Dilithio-1,3-bis(fluorenyl)propane (
6) was treated with titanium tetrachloride to yield the organic tetrabenzodispiro[4.0.4.3]tridecatetraene product
7, presumably formed by means of a carbon-carbon coupling reaction involving substituted fluorenyl radicals. The organic compounds
5 and
7 were identified by X-ray crystal structure analyses. |
---|---|
ISSN: | 0022-328X 1872-8561 |
DOI: | 10.1016/0022-328X(95)05588-G |