Enantio- and regioselective iridium-catalyzed allylic hydroxylation
The first enantioselective allylic hydroxylation to prepare branched allylic alcohols directly is described. Bicarbonate was used as nucleophile in conjunction with new single component Ir-catalysts, which are stable to air and water. Excellent regio- and enantioselectivities have been achieved with...
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| Main Authors: | , , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
January 28, 2011
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| In: |
Journal of the American Chemical Society
Year: 2011, Volume: 133, Issue: 7, Pages: 2072-2075 |
| ISSN: | 1520-5126 |
| DOI: | 10.1021/ja109953v |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/ja109953v |
| Author Notes: | Martin Gärtner, Steffen Mader, Kai Seehafer, and Günter Helmchen |
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| 520 | |a The first enantioselective allylic hydroxylation to prepare branched allylic alcohols directly is described. Bicarbonate was used as nucleophile in conjunction with new single component Ir-catalysts, which are stable to air and water. Excellent regio- and enantioselectivities have been achieved with a representative set of substrates. | ||
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