Efficient, direct alpha-methylenation of carbonyls mediated by diisopropylammonium trifluoroacetate

A very efficient method for the direct alpha-methylenation of carbonyl compounds, with yields up to 99%, utilizing paraformaldehyde, diisopropylammonium trifluoroacetate, and catalytic acid or base, is presented.

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2010-01, Vol.46 (10), p.1715-1717
Hauptverfasser: Bugarin, Alejandro, Jones, Kyle D, Connell, Brian T
Format: Artikel
Sprache:eng
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Zusammenfassung:A very efficient method for the direct alpha-methylenation of carbonyl compounds, with yields up to 99%, utilizing paraformaldehyde, diisopropylammonium trifluoroacetate, and catalytic acid or base, is presented.
ISSN:1359-7345
1364-548X
DOI:10.1039/b924577d