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A Convenient Synthesis of Trifluoromethylated Pyrroles and Porphyrins

61

Citations

4

References

1989

Year

Abstract

Abstract 4-Alkyl-3-trifluoromethyl-2-pyrrolecarboxylic acid esters (2) were conveniently prepared by the reaction of trifluoromethylated β-nitro acetates (1) with ethyl isocyanoacetate. The pyrroles were converted into the corresponding porphyrins via tetramerization of 2-(hydroxymethyl)pyrroles.

References

YearCitations

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