Abstract
Nickel(ll)-promoted rearrangement of an (N-methoxycarbonylmethy1)-substitutedp orphyrin (1) affords the nickel(ll) meso-methoxycarbonylmethylporphyrins, (3) and (4), produced by intramolecular migration of the N-substituent to carbon; when the pyrrole subunit containing the N-substituent also possesses a fi-methoxycarbonylmethyl group, 1e.g. compound (5)] a good yield of a nickel(rr) chlorin (7) is obtained.
| Original language | English |
|---|---|
| Pages (from-to) | 1498-1499 |
| Number of pages | 2 |
| Journal | Journal of the Chemical Society D: Chemical Communications |
| DOIs | |
| State | Published - 1986 |
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