Synthesis of Azaheterocyclic Vinylphosphonates by Ring??Closing Metathesis
C Garzon, M Attolini, M Maffei
Index: Garzon, Cecile; Attolini, Mireille; Maffei, Michel European Journal of Organic Chemistry, 2013 , # 18 p. 3653 - 3657
Full Text: HTML
Citation Number: 4
Abstract
Abstract The title compounds were synthesized by ruthenium-catalyzed ring-closing metathesis of N-tosyl-N-(ω-alkenyl) aminomethylvinyl phosphonates, which were obtained from N-(ω-alkenyl)-N-tosylamides. These compounds, in turn, were prepared from unsaturated alcohols through the Mitsunobu reaction. This methodology gives access to five- and six-membered ring compounds. Additionally, chiral phosphonates can be obtained ...
Related Articles:
[Lorne, Robert; Julia, Sylvestre A. Bulletin de la Societe Chimique de France, 1986 , # 2 p. 317 - 324]
Gold versus silver-catalyzed amination of allylic alcohols
[Giner, Xavier; Trillo, Paz; Najera, Carmen Journal of Organometallic Chemistry, 2011 , vol. 696, # 1 p. 357 - 361]
[Joosten, Antoine; Persson, Andreas K. A.; Millet, Renaud; Johnson, Magnus T.; Baeckvall, Jan-E. Chemistry - A European Journal, 2012 , vol. 18, # 47 p. 15151 - 15157]
[Joosten, Antoine; Persson, Andreas K. A.; Millet, Renaud; Johnson, Magnus T.; Baeckvall, Jan-E. Chemistry - A European Journal, 2012 , vol. 18, # 47 p. 15151 - 15157]
Reactions of n-sulfinyl-p-toluenesulfonamide with alcohols
[McFarland, John W.; Schut, Dirk; Zwanenburg, Binne Tetrahedron, 1981 , vol. 37, p. 389 - 393]