Title
One-pot synthesis of regiochemically pure porphyrins from two different pyrroles
Document Type
Article
Publication Date
10-10-1994
Abstract
Treatment of 2,5-di-unsubstituted pyrroles (e.g. 10) with excess of Eschenmoser's reagent (N,N-dimethylmethyleneammonium iodide) affords 2,5-bis-(N,N-dimethylaminomethy)pyrroles (e.g. 7); reaction with a second 2,5-di-unsubstituted pyrrole (e.g. 8) gives pure porphyrin (e.g. 9) with identical substituents on opposite pyrrole sub-units. © 1994.
Publication Source (Journal or Book title)
Tetrahedron Letters
First Page
7581
Last Page
7584
Recommended Citation
Nguyen, L., Senge, M., & Smith, K. (1994). One-pot synthesis of regiochemically pure porphyrins from two different pyrroles. Tetrahedron Letters, 35 (41), 7581-7584. https://doi.org/10.1016/S0040-4039(00)78348-1
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