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Imenes derived from methylsulphonyl‐acetonitrile: (Properties of the sulphonyl group XLIII)
15
Citations
7
References
1954
Year
Inorganic ChemistryChemical EngineeringCcnch 3EngineeringHeterocyclicDerivative (Chemistry)Organic Material ChemistryType Rso 2Organic ChemistrySynthetic ChemistryChemistrySulphonyl Group XliiiChemical DerivativeNitrogen AtomEnantioselective SynthesisBiomolecular EngineeringInorganic Compound
Abstract When reacting diazomethane on nitriles of the type RSO 2 ‐CHXCN, where X is a negative group, methylation on the nitrogen atom often occurs. In the case of bis‐methylsulphonyl‐acetonitrile, the N‐methyl derivative is formed exclusively: (CH 3 SO 2 ) 2 CCNCH 3 . The less acidic methylsulphoxyl‐methylsulphonyl‐acetonitrile forms only the C‐methyl derivative: (CH 3 SO)(CH 3 SO 2 )C(CH 3 )CN.
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