Abstract
A new total synthesis of a protoporphyrin IX derivative in which the α-methylene protons of the 13,17-(2-methoxycarbonylethyl) substituents are regioselectively deuterated is described. The deuterated porphyrin was obtained using the oxidative cyclization of an a, c-biladiene dihydrobromide. Copyright (C) 2000 John Wiley and Sons, Ltd.
| Original language | English |
|---|---|
| Pages (from-to) | 185-191 |
| Number of pages | 7 |
| Journal | Journal of Porphyrins and Phthalocyanines |
| Volume | 4 |
| Issue number | 2 |
| DOIs | |
| State | Published - Mar 2000 |
Keywords
- a, c-biladienes
- Deuterium labeling
- Heme proteins
- Porphyrin synthesis
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