1343479-84-4Relevant academic research and scientific papers
1,2-dihydropentalenes from fulvenes by [6 + 2] cycloadditions with 1-isopropenylpyrrolidine
Coskun, Necdet,Ma, Jingxiang,Azimi, Saeed,Gaertner, Christian,Erden, Ihsan
, p. 5952 - 5955 (2011)
In situ generated acetone pyrrolidine enamine undergoes [6 + 2] cycloadditions with fulvenes to give 1,2-dihydropentalenes. This ring annulation method works particularly well with 6-monosubstituted fulvenes and is subject to steric hindrance at C-6 of th
