Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2481
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dc.contributor.authorAdhikari, D.-
dc.date.accessioned2020-12-02T06:33:23Z-
dc.date.available2020-12-02T06:33:23Z-
dc.date.issued2016-
dc.identifier.citationOrganometallics, 35(17), pp.2930–2937.en_US
dc.identifier.otherhttps://doi.org/10.1021/acs.organomet.6b00478-
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/acs.organomet.6b00478-
dc.identifier.urihttp://hdl.handle.net/123456789/2481-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractA base-metal, Fe(0)-catalyzed hydrosilylation of imines to obtain amines is reported here which outperforms its noble-metal congeners with the highest TON of 17000. The catalyst, (aNHC)Fe(CO)4, works under very mild conditions, with extremely low catalyst loading (down to 0.005 mol %), and exhibits excellent chemoselectivity. The facile nature of the imine reduction under mild conditions has been further demonstrated by reducing imines towards expensive commercial amines and biologically important N-alkylated sugars, which are difficult to achieve otherwise. A mechanistic pathway and the source of chemoselectivity for imine hydrosilylation have been proposed on the basis of the well-defined catalyst and isolable intermediates along the catalytic cycle.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectCatalyzeden_US
dc.subjectHydrosilylationen_US
dc.subjectExhibitsen_US
dc.subjectChemoselectivityen_US
dc.titleA Highly Efficient Base-Metal Catalyst: Chemoselective Reduction of Imines to Amines Using An Abnormal-NHC–Fe(0) Complexen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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