Intramolecular 1,3-dipolar cycloadditions of norbornadiene-tethered nitrones.

  title={Intramolecular 1,3-dipolar cycloadditions of norbornadiene-tethered nitrones.},
  author={Geoffrey K Tranmer and W Vanessa Tam},
  journal={The Journal of organic chemistry},
  volume={66 15},
Efficient routes to the synthesis of norbornadiene-tethered nitrones have been developed, and their intramolecular 1,3-dipolar cycloadditions were studied. The cycloadditions occurred in moderate to good yields for a variety of substrates and were found to be highly regio- and stereoselective, giving single regio- and stereoisomers in most cases. 

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