Three Coordinated Organoaluminum Cation for Rapid and Selective Cyanosilylation of Carbonyls under Solvent‐Free Conditions

dc.contributor.authorRawat, S.
dc.contributor.authorBhandari, M.
dc.contributor.authorPrashanth, B.
dc.contributor.authorSingh, Sanjay
dc.date.accessioned2021-01-02T06:12:33Z
dc.date.available2021-01-02T06:12:33Z
dc.date.issued2020
dc.description.abstractThe well-defined three coordinated electronically unsaturated cationic organoaluminum complex [({(2,6-iPr2C6H3N)P(Ph2)}2N)AlMe]+[MeB(C6F5)3]− (1), has been utilized to catalyze the cyanosilylation of aldehydes and ketones under mild and solvent-free conditions. Moreover, catalyst 1 showed high chemoselective cyanosilylation of aldehydes over ketones, nitriles and olefins. The multinuclear NMR investigations revealed that cyanosilylation proceeds via Lewis adduct formation between 1 and TMSCN thereby activating TMSCN (Si-CN bond) followed by nucleophilic attack of the carbonyl oxygen at the Si center of the activated silane and formation of the product.en_US
dc.identifier.citationChemCatChem, 12(9), pp.2407-2411.en_US
dc.identifier.otherhttps://doi.org/10.1002/cctc.202000309
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cctc.202000309
dc.identifier.urihttp://hdl.handle.net/123456789/3480
dc.language.isoenen_US
dc.publisherWiley Blackwellen_US
dc.subjectCarbonylen_US
dc.subjectCationic aluminum complexen_US
dc.subjectChemoselectivityen_US
dc.subjectCyanosilylationen_US
dc.subjectOrganoaluminum catalysten_US
dc.titleThree Coordinated Organoaluminum Cation for Rapid and Selective Cyanosilylation of Carbonyls under Solvent‐Free Conditionsen_US
dc.typeArticleen_US

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