| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10572710 | Journal of Fluorine Chemistry | 2010 | 4 Pages |
Abstract
Selected N-alkyl ketoimines having at least one methyl group at the imino carbon were reacted in a Stork enamine reaction with 2,2-difluoro-2-fluorosulfonylacetyl fluoride to yield enaminones carrying one fluorosulfonyldifluoromethylene function. In the case of N-tertbutyl methyl aldimine two of these groups were present in a triketone derivative. Taking a ethylene bis(imine) also a ring closure reaction was observed, proven by X-ray structure analysis.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Katja Vlasov, Nataliya Kalinovich, Enno Lork, Gerd-Volker Röschenthaler,