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The synthesis of highly functionalized pyrroles: A challenge in regioselectivity and chemical reactivity

Journal

SYNTHESIS-STUTTGART
Volume -, Issue 20, Pages 3095-3110

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-2007-990783

Keywords

pyrroles; heterocycles; cyclizations; regioselectivity; radical reactions

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Pyrrole-containing compounds play an eminent role in nature. Since the development of the pyrrole synthesis by Knorr and Paal at the end of the I 9(th) century, the synthesis and study of modified pyrroles has become an active field of chemical research spanning from natural product synthesis, through medicinal chemistry, and on to material science. For example, the synthetic availability of porphyrins and their artificial analogues and isomers in the second half of the last century led to important insights into the function of this prominent molecule in nature. In the last few years, synthetic pyrrole-containing biomacromolecules and intelligent materials such as pyrrole-based conducting polymers have come into focus. All this research requires the efficient synthesis of highly functionalized pyrroles. However, even after more than 100 years since the pioneering work by Paal and Knorr, the synthesis of highly functionalized pyrroles remains challenging. Often, the yields are low and the regioselectivity is only rnodest. We present here an overview of some recent work in this area, including some of our own research.

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