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Nickel(II)-promoted rearrangements of Some N-substituted porphyrins

  • University of California at Davis

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

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 languageEnglish
Pages (from-to)1498-1499
Number of pages2
JournalJournal of the Chemical Society D: Chemical Communications
DOIs
StatePublished - 1986

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