Enantio- and regioselective iridium-catalyzed allylic esterification
A highly enantioselective and regioselective Ir-catalyzed allylic esterification is described, in which branched allylic esters are synthesized directly. Carboxylates were used as nucleophiles and linear allylic phosphates as electrophiles. In some cases the allylic substitution reaction was found t...
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| Main Authors: | , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
January 14, 2014
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| In: |
Journal of the American Chemical Society
Year: 2014, Volume: 136, Issue: 4, Pages: 1272-1275 |
| ISSN: | 1520-5126 |
| DOI: | 10.1021/ja411869r |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/ja411869r Verlag, lizenzpflichtig, Volltext: https://pubs.acs.org/doi/10.1021/ja411869r 
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| Author Notes: | Jianping Qu, Lydia Roßberg, and Günter Helmchen |
| Summary: | A highly enantioselective and regioselective Ir-catalyzed allylic esterification is described, in which branched allylic esters are synthesized directly. Carboxylates were used as nucleophiles and linear allylic phosphates as electrophiles. In some cases the allylic substitution reaction was found to be accompanied by a kinetic resolution process, which causes a change of the enantiomeric excess. |
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| Item Description: | Gesehen am 12.10.2020 |
| Physical Description: | Online Resource |
| ISSN: | 1520-5126 |
| DOI: | 10.1021/ja411869r |