@article{pittir19947,
          volume = {5},
          number = {18},
           month = {September},
          author = {S Werner and DP Curran},
           title = {Fluorous dienophiles are powerful diene scavengers in diels-alder reactions},
         journal = {Organic Letters},
           pages = {3293 -- 3296},
            year = {2003},
             url = {http://d-scholarship-dev.library.pitt.edu/19947/},
        abstract = {(Matrix presented) Three fluorous dienophiles have been synthesized, and their value in scavenging an excess diene after Diels-Alder reactions is shown. The resulting fluorous derivatives are separated by solid-phase extraction on fluorous silica gel (FSPE). The fluorous [1,2,4]triazoline-3,5-dione 10 reacted with most dienes within seconds or minutes.}
}