Issue 3, 1994

Synthesis of β-aryl substituted porphyrins by palladium-catalysed cross-coupling reactions

Abstract

β-Bromoporphyrins undergo Suzuki cross-coupling reactions with aryl boronic acids to give β-arylporpyrins in high yields and X-ray analysis shows that H2TPP(Ph)42a(TPP = tetraphenylporphyrin) is centrosymmetric and possesses a hydrogen-bonded inner core.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 271-272

Synthesis of β-aryl substituted porphyrins by palladium-catalysed cross-coupling reactions

K. S. Chan, X. Zhou, B. Luo and T. C. W. Mak, J. Chem. Soc., Chem. Commun., 1994, 271 DOI: 10.1039/C39940000271

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