# metadata.dc.description.abstract[].value
A new synthetic routes to the triaryl pyrrolo[2,3-d]pyrimidines from common 4,6-dichloropyrimidine have been developed. The triarylated compounds are synthesized by three cross-coupling reactions using three different catalysts. The introduction of C-6-aryl was allowed in two step process using Sonogashira conditions followed by intramolecular cyclization and the Suzuki-Miyaura conditions led the C-4 and C-5 diarylation. This sequence allows a flexible approach to the highly arylated pyrrolopyrimidines containing different aryl groups

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European Journal of Organic Chemistry, 2014, vol. 2014, num. 7, p. 1514-1524

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Articles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)