Abstract
Oxidative cyclization of open chain thiabilanes yielded the first examples of unique piperazine bridged thianorrole dimers instead of the expected thianorrole monomer. In the thianorrole dimer, the two thianorrole monomeric units are linked via two direct pyrrole C-C bonds by involving the inverted pyrrole and adjacent pyrrole rings of each thianorrole macrocycle and generate a six-membered piperazine ring that bridges the two thianorrole macrocycles. The spectral studies indicated that the thianorrole dimers are nonaromatic in nature.
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