Next Article in Journal
A Simple Enzymatic Preparation of 2’,3’-Di-OAcetylnucleosides Through a Lipase Catalyzed Alcoholysis
Previous Article in Journal
Synthesis of Diads and Triads Derived from Carotenoids and Fullerene C60
Article Menu

Article Versions

Export Article

Open AccessAbstract
Molecules 2000, 5(3), 531-532; doi:10.3390/50300531

Synthesis of Asymmetrical Porphyrins Substituted in the meso-Position from Dipyrrolomethanes

Departamento de Química y Física, Universidad Nacional de Río Cuarto, Agencia Postal Nº 3, 5800 Río Cuarto, Argentina
Author to whom correspondence should be addressed.
Published: 22 March 2000
Download PDF [15 KB, uploaded 18 June 2014]


A convenient procedure for the synthesis of 5-(4-acetamidophenyl)-10,15,20-tris(4-substituted phenyl) porphyrins from dipyrrolomethane is reported. meso-(4-Substituted phenyl) dipyrrolomethanes were obtained in yields of 72-84%. The amide porphyrins were isolated with appreciable yields of 15-17%.
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

Scifeed alert for new publications

Never miss any articles matching your research from any publisher
  • Get alerts for new papers matching your research
  • Find out the new papers from selected authors
  • Updated daily for 49'000+ journals and 6000+ publishers
  • Define your Scifeed now

SciFeed Share & Cite This Article

MDPI and ACS Style

Milanesio, E.; Chiacchiera, S.M.; Silber, J.J.; Durantini, E.N. Synthesis of Asymmetrical Porphyrins Substituted in the meso-Position from Dipyrrolomethanes. Molecules 2000, 5, 531-532.

Show more citation formats Show less citations formats

Related Articles

Article Metrics

Article Access Statistics



[Return to top]

Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert
Back to Top