Abstract
When meso-dimethylaminomethyletioporphyrin I (I) is heated in CCl4 or tetrahydrofuran (THF) in the presence of zinc acetate, it reacts with alcohols to give the corresponding meso-alkoxy-methylporphyrins. Under similar conditions CH acids (acetone, acetylacetone, nitromethane, and others) form the corresponding meso-substituted derivatives with the formation of a C-C bond. Ethers are formed when the copper and nickel complexes of I are heated in ethylene glycol.
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See [1] for Communication 12.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 943–948, July, 1980.
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Ponomarev, G.V. Porphyrins. 13. Reaction of meso-dimethylaminomethyletioporphyrin I with nucleophiles in the presence of zinc acetate. Chem Heterocycl Compd 16, 730–735 (1980). https://doi.org/10.1007/BF00557748
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DOI: https://doi.org/10.1007/BF00557748