Title
Benzoporphyrins via an olefin ring-closure metathesis methodology
Document Type
Article
Publication Date
1-1-2006
Abstract
A new route to benzoporphyrins is reported in which readily available vicinal dibromoporphyrins are bis-allylated using the Suzuki reaction, cyclized by way of olefin metathesis and finally oxidized to give mono-, di-, or tri-benzoporphyrins. © The Royal Society of Chemistry 2006.
Publication Source (Journal or Book title)
Chemical Communications
First Page
3900
Last Page
3902
Recommended Citation
Jiao, L., Hao, E., Fronczek, F., Vicente, M., & Smith, K. (2006). Benzoporphyrins via an olefin ring-closure metathesis methodology. Chemical Communications (37), 3900-3902. https://doi.org/10.1039/b607711k