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A direct synthetic method for some 2,5-and 2.6-crosslinked chlorinated tetrahydromethano-indanes, which are the most important conversion products of cyclodiene insecticides under abiotic conditions, is described. The structures of the resulting compounds are confirmed with the aid of MS and  1 H NMR.

Zur Synthese von 2.5-und 2.6-verbrückten Tetrahydromethanoindanen / Synthesis of 2,5-and 2,6-Crosslinked Tetrahydromethanoindanes