Abstract
A rationally designed mechanistic approach to anti-Markovnikov olefin hydrofunctionalization and its application to the synthesis of heterocycles are described. Porphyrin-rhodium complexes have been shown to exhibit remarkable reactivity and selectivity for each step of the proposed catalytic cycle (see scheme). A critical step of this reaction sequence is a new, facile, and remarkably general carbon-heteroatom bond-forming reductive elimination.
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Sanford, M. S., & Groves, J. T. (2004). Anti-Markovnikov Hydrofunctionalization of Olefins Mediated by Rhodium-Porphyrin Complexes. Angewandte Chemie - International Edition, 43(5), 588–590. https://doi.org/10.1002/anie.200351941
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