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Volumn 52, Issue 5, 1987, Pages 827-836

Rothemund and Adler-Longo Reactions Revisited: Synthesis of Tetraphenylporphyrins under Equilibrium Conditions

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EID: 0006368032     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00381a022     Document Type: Article
Times cited : (1452)

References (33)
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    • Though we have no evidence that porphyrinogen is quantitatively converted to porphyrin, the yield must be quite high. An 80% overall yield was reported for the series of manipulations including catalytic reduction of a porphyrin to form the porphyrinogen, DDQ oxidation to give the porphyrin, chromatography, and crystallization. See
    • Though we have no evidence that porphyrinogen is quantitatively converted to porphyrin, the yield must be quite high. An 80% overall yield was reported for the series of manipulations including catalytic reduction of a porphyrin to form the porphyrinogen, DDQ oxidation to give the porphyrin, chromatography, and crystallization. See: Cavaleiro, J. A. S.; Rocha Gonsalves, A. M.; Kenner, G. W.; Smith, K. M. J. Chem. Soc. Perkin Trans. 1 1974, 1771.
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  • 32


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