Pyrrole studies. Part 44. Synthesis of potentially biologically active pyrroloylanilines

Article abstract of DOI:10.1080/00397919308009838

The direct reaction of acid labile pyrrolecarboxylic acids with anilines in the presence of N,N'-dicyclohexylcarbodiimide provides an efficient general synthesis of pyrroloylanilines.

Full text of DOI:10.1080/00397919308009838

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Synthetic Communications: An
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Pyrrole Studies. Part. 44.1
Synthesis of Potentially
Biologically Active
Pyrroloylanilines
R. A. Jones a , D. C. Rustidge a & R. Sarin a
a School of Chemical Sciences, University of East
Anglia , Norwich, NR4 7TJ, UK
Published online: 23 Sep 2006.
To cite this article: R. A. Jones , D. C. Rustidge & R. Sarin (1993) Pyrrole Studies.
Part. 44.1 Synthesis of Potentially Biologically Active Pyrroloylanilines, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 23:6, 771-777
To link to this article: http://dx.doi.org/10.1080/00397919308009838
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