Synlett 2000; 2000(2): 213-216
DOI: 10.1055/s-2000-6504
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Synthesis of Novel Pyrrolic Compounds from Nitroarenes and Isocyanoacetates Using a Phosphazene Superbase

Timothy D. Lash* , Michelle L. Thompson, Tonya M. Werner, John D. Spence
  • *Department of Chemistry, Illinois State University, Normal, Illinois 61790-4160, USA; E-mail: tdlash@ilstu.edu
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Utilization of a phosphazene base allows hitherto unreactive nitroaromatic compounds to condense with ethyl isocyanoacetate to give c-annelated pyrroles. On the other hand, 3-nitropyridine reacted under these conditions to give a novel tricyclic heterocycle 13 in modest yield.

    >