Prieur, VanessaRubio Martínez, JaimeFont Bardia, Ma. MercedesGuillaumet, GéraldPujol Dilmé, M. Dolors2020-06-152020-06-152014-02-021434-193Xhttps://hdl.handle.net/2445/165543A 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 groups31 p.application/pdfeng(c) Wiley-VCH, 2014NitrogenMicroonesNitrogenMicrowavesinfo:eu-repo/semantics/article6364822020-06-15info:eu-repo/semantics/openAccess