352311-22-9Relevant academic research and scientific papers
Enamide-benzyne-[2 + 2] cycloaddition: Stereoselective tandem [2 + 2]-pericyclic ring-opening-intramolecular N-tethered [4 + 2] cycloadditions
Feltenberger, John B.,Hayashi, Ryuji,Tang, Yu,Babiash, Eric S.C.,Hsung, Richard P.
supporting information; experimental part, p. 3666 - 3669 (2011/02/25)
Image Presented Benzyne-[2 + 2] cycloadditions with enamides are described. This effort led to the development of a highly stereoselective tandem [2 + 2] cycloaddition-pericyclic ring-opening-intramolecular-N-tethered-[4 + 2] cycloaddition for rapid assembly of nitrogen heterocycles.
Enamide-Olefin Ring-Closing Metathesis
Kinderman, Sape S.,Van Maarseveen, Jan H.,Schoemaker, Hans E.,Hiemstra, Henk,Rutjes, Floris P. J. T.
, p. 2045 - 2047 (2007/10/03)
(matrix presented) The first examples of ring-closing metathesis reactions of olefin-containing enamides using ruthenium-based catalysts have been demonstrated. A preliminary investigation into the scope and limitations, leading to protected five- and six-membered cyclic enamides, will be presented.
