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Rh-bound trimethylenemethane variants generated from the interaction of a Rh-carbenoid with an allene have been applied to the synthesis of substituted 3,4-fused pyrroles. The pyrrole products are useful starting points for the syntheses of various dipyrromethene ligands. Furthermore, the methodology has been applied to a synthesis of the natural product cycloprodigiosin, which demonstrates antitumor and immunosuppressor activity.

Citation

Erica E Schultz, Richmond Sarpong. Application of in situ-generated Rh-bound trimethylenemethane variants to the synthesis of 3,4-fused pyrroles. Journal of the American Chemical Society. 2013 Mar 27;135(12):4696-9

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PMID: 23477843

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