Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/ja0676758 | DOI Listing |
Chem Commun (Camb)
August 2013
CNRS, UMR 5253, Institut Charles Gerhardt Montpellier AM2N, ENSCM, 8, rue de l'Ecole Normale, 34296 Montpellier Cedex 5, France.
The N-cyclopropylation of aromatic and aliphatic secondary acyclic amides, known to be poor nucleophiles, has been accomplished using a simple and cheap copper system. The corresponding tertiary acyclic amides, which constitute a wide family of biologically active compounds, have been obtained in good to excellent yields.
View Article and Find Full Text PDFJ Am Chem Soc
January 2007
Boehringer Ingelheim (Canada) Ltd. Research and Development, 2100 rue Cunard, Laval (Québec) Canada, H7S 2G5.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!