Journal of the American Chemical Society, Vol.117, No.7, 1954-1964, 1995
A New Strategy to Bicyclo(5.3.0)Decenes via Anionic Intramolecular Ring-Opening of Oxabicyclo(3.2.1) Compounds
Intramolecular anionic ring opening of oxabicyclo[3.2.1] systems has been achieved and leads to an efficient route to bicyclo[5.3.0]decenes which are trans fused. Tethers containing heteroatoms (X = O, S, NMe) as well as all-carbon derivatives have been successfully cyclized under these conditions. It is not necessary to take any special precautions (high dilution, slow addition etc.) when carrying out the transmetalation-cyclization since intermolecular ring opening does not occur under these conditions.
Keywords:PROTEIN-KINASE-C;TUMOR PROMOTERS;STEREOSELECTIVE SYNTHESIS;ORGANOLITHIUM REAGENTS;OXABICYCLIC COMPOUNDS;ACYCLIC COMPOUNDS;CYCLIZATION;DERIVATIVES;PHORBOL;ROUTE