Copper-catalyzed rearrangement of vinyl oxiranes
…, CE McInnis, JT Njardarson
Index: Batory, Lindsay A.; McInnis, Christine E.; Njardarson, Jon T. Journal of the American Chemical Society, 2006 , vol. 128, # 50 p. 16054 - 16055
Full Text: HTML
Citation Number: 43
Abstract
A novel copper-catalyzed vinyl oxirane ring expansion protocol has been developed. A wide range of vinyl oxiranes can be rearranged to 2, 5-dihydrofurans in excellent yields in the presence of electrophilic copper (II) acetylacetonate catalysts. Regioisomeric vinyl oxiranes can be converted to a single dihydrofuran product using these conditions. This method uses low catalyst loadings (0.5-5 mol%), has good tolerance of substitution patterns, and can ...
Related Articles:
[Laskavy, Alexander; Shimon, Linda J. W.; Konstantinovski, Leonid; Iron, Mark A.; Neumann, Ronny Journal of the American Chemical Society, 2010 , vol. 132, # 2 p. 517 - 523]
[Brennfuehrer, Anne; Neumann, Helfried; Klaus, Stefan; Riermeier, Thomas; Almena, Juan; Beller, Matthias Tetrahedron, 2007 , vol. 63, # 27 p. 6252 - 6258]
[Gosselin, Pascal; Bourdy, Christophe; Mille, Stephane; Perrotin, Angelique Journal of Organic Chemistry, 1999 , vol. 64, # 26 p. 9557 - 9565]
[Kocienski,P.J.; Ciabattoni,J. Journal of Organic Chemistry, 1974 , vol. 39, # 3 p. 388 - 393]
[Closs,G.L.; Closs,L.E. Journal of the American Chemical Society, 1963 , vol. 85, p. 99 - 104]