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Metal-Free Entry to Phosphonylated Isoindoles by a Cascade of 5-exo-dig Cyclization, a [1,3]-Alkyl Shift, and Aromatization under Microwave Heating.

When o-ethynylbenzyl alpha-aminophosphonates are heated under microwave conditions, a rearrangement occurs which results in the formation of phosphonylated isoindoles. The rearrangement consists of a 5-exo-dig cyclization followed by a [1,3]-alkyl shift and finally aromatization.[1]

References

  1. Metal-Free Entry to Phosphonylated Isoindoles by a Cascade of 5-exo-dig Cyclization, a [1,3]-Alkyl Shift, and Aromatization under Microwave Heating. Dieltiens, N., Stevens, C.V. Org. Lett. (2007) [Pubmed]
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