Enantioselective intramolecular CH-insertions upon Cu-catalyzed decomposition of phenyliodonium ylides

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Abstract

The Cu-catalyzed intramolecular CH insertion of phenyliodonium ylide 5b has been investigated at 0° C in the presence of several chiral ligands. Enantioselectivities vary in the range of 38-72 %, and are higher than those resulting from reaction of the diazo compound 5c at 65° C. The results are consistent with a carbenoid mechanism for Cu-catalyzed decomposition of phenyliodonium ylides.

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Müller, P., & Boléa, C. (2001). Enantioselective intramolecular CH-insertions upon Cu-catalyzed decomposition of phenyliodonium ylides. In Molecules (Vol. 6, pp. 258–266). Molecular Diversity Preservation International. https://doi.org/10.3390/60300258

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