Solvent-free Diels–Alder reactions of in situ generated cyclopentadiene
D Huertas, M Florscher, V Dragojlovic
Index: Huertas, David; Florscher, Melinda; Dragojlovic, Veljko Green Chemistry, 2009 , vol. 11, # 1 p. 91 - 95
Full Text: HTML
Citation Number: 21
Abstract
A solvent-free Diels–Alder reaction was carried out by heating a mixture of dicyclopentadiene and a dienophile. Cyclopentadiene, formed in situ, reacted with the dienophile in a thermodynamically controlled reaction. Besides being solvent-free, the described procedure allows for almost complete utilization of dicyclopentadiene and avoids handling of noxious and hazardous cyclopentadiene. The reaction worked well with ...
Related Articles:
[Pandey; Saravanan; Rao; Nagamani; Kumar Tetrahedron Letters, 1995 , vol. 36, # 7 p. 1145 - 1148]
[Marchand, Alan P.; Suri, Suresh Chander; Earlywine, Arthur D.; Powell, Douglas R.; Helm, Dick van der Journal of Organic Chemistry, 1984 , vol. 49, # 4 p. 670 - 675]
[Stoermer, Martin J.; Butler, Douglas N.; Warrener, Ronald N.; Weerasuria; Fairlie, David P. Chemistry - A European Journal, 2003 , vol. 9, # 9 p. 2068 - 2071]
[Stoermer, Martin J.; Butler, Douglas N.; Warrener, Ronald N.; Weerasuria; Fairlie, David P. Chemistry - A European Journal, 2003 , vol. 9, # 9 p. 2068 - 2071]
[Stoermer, Martin J.; Butler, Douglas N.; Warrener, Ronald N.; Weerasuria; Fairlie, David P. Chemistry - A European Journal, 2003 , vol. 9, # 9 p. 2068 - 2071]