Preparation of 2-alkyl-and 2-acylpropenals from 5-(trifluoromethanesulfonyloxy)-4H-1, 3-dioxin: a versatile acrolein α-cation synthon
SP Fearnley, RL Funk, RJ Gregg
Index: Fearnley, Stephen P.; Funk, Raymond L.; Gregg, Robert J. Tetrahedron, 2000 , vol. 56, # 52 p. 10275 - 10281
Full Text: HTML
Citation Number: 13
Abstract
5-(Trifluoromethanesulfonyloxy)-4H-1, 3-dioxin (3) participates in a variety of nucleophilic substitution reactions with cuprate reagents or in palladium catalyzed cross-coupling reactions to provide 5-substituted-4H-1, 3-dioxins 5. Upon thermolysis, these compounds undergo facile retrocycloaddition reactions to generate the corresponding 2-substituted acroleins which, if necessary, can be trapped in situ with dienes or heterodienophiles. In ...
Related Articles:
[Goettmann, Frederic; Le Floch, Pascal; Sanchez, Clement Chemical Communications, 2006 , # 2 p. 180 - 182]
[Walling, Cheves; El-Taliawi, Gamil M.; Amarnath, Kalyani Journal of the American Chemical Society, 1984 , vol. 106, p. 7573 - 7578]
[Sawaki, Yasuhiko; Ogata, Yoshiro Journal of the American Chemical Society, 1981 , vol. 103, # 21 p. 6455 - 6460]
[Newmann-Evans, Richard H.; Simon, Reyna J.; Carpenter, B. K. Journal of Organic Chemistry, 1990 , vol. 55, # 2 p. 695 - 711]
[Najera, Carmen; Sansano, Jose Miguel Tetrahedron, 1990 , vol. 46, # 11 p. 3993 - 4002]