Ligand‐Controlled Regiodivergent and Enantioselective Copper‐Catalyzed Hydroallylation of Alkynes
A ligand‐controlled regiodivergent and enantioselective copper‐catalyzed intermolecular hydroallylation of alkynes with allylic phosphates and hydrosilanes has been achieved for the first time. The chiral bidentate sulfonate‐containing N‐heterocyclic carbene ligated CuCl complex leads to enantioenri...
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Veröffentlicht in: | Angewandte Chemie International Edition 2017-10, Vol.56 (42), p.13130-13134 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A ligand‐controlled regiodivergent and enantioselective copper‐catalyzed intermolecular hydroallylation of alkynes with allylic phosphates and hydrosilanes has been achieved for the first time. The chiral bidentate sulfonate‐containing N‐heterocyclic carbene ligated CuCl complex leads to enantioenriched SN2′‐type products, whereas the use of the IMesCuCl catalyst affords SN2‐type products. Thus a range of chiral branched and achiral linear 1,4‐dienes could be facilely synthesized from readily available alkynes in a regiodivergent manner.
Under control: A ligand‐controlled regiodivergent and enantioselective copper‐catalyzed intermolecular hydroallylation of alkynes with allylic phosphates and hydrosilanes has been achieved. Chiral branched or achiral linear dienes can be obtained by proper choice of the ancillary N‐heterocyclic carbene ligand. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201707070 |