Journal of Organic Chemistry p. 5078 - 5088 (1990)
Update date:2022-08-03
Topics:
Rigby, James H.
Kotnis, Atul
Kramer, James
General protocols for the construction of various ring systems employing cation olefin cyclizations initiated by the readily accessible 1,3-benzodithiolium ion are described.Several substituted tetralones and tetralins can be rapidly assembled by this methodology as can a variety of substituted bicyclo<3.2.1>octane and tricyclic ring systems.The products of these transformations are amenable to interconversion into a range of functionalized species.
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