The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: Selective C-N bond formation and N-O bond cleavage in one-pot for α-amination of ketones

Chemical Communications

Volumn 51, Issue 73, 2015, Pages 13976-13979

  Ramakrishna, Isai ^a   Grandhi, Gowri Sankar ^a   Sahoo, Harekrishna ^a   Baidya, Mahiuddin ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY MADRAS   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOKETONE; CARBON; CARBONYL DERIVATIVE; ETHER DERIVATIVE; MENTHOL; NITROGEN; NITROSO DERIVATIVE; NITROSOCARBONYL DERIVATIVE; OXYGEN; SILANE DERIVATIVE; SILYL ENOL ETHER; SOLVENT; UNCLASSIFIED DRUG; ACETONITRILE; ACETONITRILE DERIVATIVE; COPPER; CUPRIC CHLORIDE; KETONE; PYRIDINE DERIVATIVE;

AMINATION; ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CHIRALITY; CONTROLLED STUDY; COVALENT BOND; DIASTEREOISOMER; MUKAIYAMA REACTION; ONE POT SYNTHESIS; REACTION TIME; SILYLATION; STEREOCHEMISTRY; CHEMISTRY;

ACETONITRILES; AMINATION; COPPER; KETONES; NITROSO COMPOUNDS; OXYGEN; PYRIDINES;

EID: 84940490630     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c5cc05459a     Document Type: Article

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