Solvent-Free Organocatalytic Mukaiyama-Michael Addition of 2-Trimethylsilyloxy Furan to Nitroalkenes Catalyzed by Brønsted Acids
Academic Article
Publication Date:
2009
abstract:
The first organocatalytic Mukaiyama-Michael addition of 2-trimethylsilyloxy furan to nitroalkenes was promoted by Brønsted acids under solvent-free conditions. The conjugate addition took place in moderate to good yields with variously substituted nitroalkenes. The procedure is operationally simple and no workup is required.
Iris type:
01.01 Articolo in rivista
Keywords:
solvent-free; conjugate addition; Brønsted acids; nitroalkenes; 2-trimethylsilyloxy furan
List of contributors:
Villano, Rosaria
Published in: