4.8 Article

Efficient Synthesis of Hangman Porphyrins

Journal

ORGANIC LETTERS
Volume 12, Issue 5, Pages 1036-1039

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol902947h

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Funding

  1. Fannie and John Hertz Foundation
  2. Office of Basic Energy Sciences of the U.S. Department of Energy [DE-FG02-05ER15745]

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A two-step synthetic method has been designed to furnish hangman porphyrins in good yields from easily available starting materials. The use of the microwave irradiation technique has been found to be valuable for delivering the carboxylic acid hanging group in a much simplified and less time-consuming basic ester hydrolysis (4 h vs 7 days under harsh acidic conditions). The new route facilitates the synthesis of various hangman porphyrins that previously had limited or no access.

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