Asymmetric Base-Free Michael Addition at Room Temperature with Nickel-Based Bifunctional Amido-Functionalized N-Heterocyclic Carbene Catalysts
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Title |
Asymmetric Base-Free Michael Addition at Room Temperature with Nickel-Based Bifunctional Amido-Functionalized N-Heterocyclic Carbene Catalysts
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Creator |
RAO, MN
HARIDAS, M GANGWAR, MK RAJAKANNU, P KALITA, AC GHOSH, P |
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Subject |
PINCER PALLADIUM COMPLEXES
CINCHONA ALKALOIDS ORGANIC-MOLECULES AMINE-THIOUREA STEREOCENTERS LIGANDS REGIOSELECTIVITY NITROOLEFINS CONSTRUCTION CHEMISTRY Asymmetric catalysis Michael addition Bifunctional catalysts Carbene ligands Nickel |
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Description |
A series of nickel-based chiral bifunctional catalysts (1d-3d) with N-heterocyclic carbene (NHC) ligands derived from (1R)-(-)-menthol, (1S)-(-) pinene, and (1R)-(+)-camphor have been successfully designed for asymmetric Michael addition reactions under base-free conditions. The NHC complexes, namely, [1-R-3-{N-(phenylacetamido)}imidazol-2-ylidene](2)-Ni [R = (1S)-menthyl (1d), (1S)-pinane (2d), and (1R)-isobornyl (3d)], bearing chiral ancillaries on the amido-functionalized side arms of the NHC ligands, performed the bifunctional catalysis of the asymmetric base-free Michael addition reaction of the alpha-methyl cyano ester substrates ethyl 2-cyano-propanoate (4), isopropyl 2-cyanopropanoate (5), and tertbutyl 2-cyanopropanoate (6) with the activated olefinic substrates methyl vinyl ketone (7) and acrylonitrile (8) in 63-98% yields with enantiomeric excess (ee) values of 2-75% at room temperature in 8 h. More interestingly, only the longest of the three catalysts, the menthol derivative 1d, showed significant chiral induction of up to 75% ee; this has been attributed to the reduction of the steric influence owing to the relatively distant dispositions of the chiral ancillaries from the catalytically active metal center that arise as a consequence of the cis geometries of 1d-3d.
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Publisher |
WILEY-V C H VERLAG GMBH
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Date |
2016-01-14T10:35:15Z
2016-01-14T10:35:15Z 2015 |
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Type |
Article
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Identifier |
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY(9)1604-1615
1434-1948 1099-0682 http://dx.doi.org/10.1002/ejic.201403224 http://dspace.library.iitb.ac.in/jspui/handle/100/17373 |
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Language |
en
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