Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine from N 1 ‐Alkyne‐1,2‐diamines
Ist Teil von
Chemistry : a European journal, 2015-12, Vol.21 (51), p.18828-18833
Erscheinungsjahr
2015
Quelle
Wiley-Blackwell Full Collection
Beschreibungen/Notizen
Abstract
A one‐pot protocol for the diversity oriented synthesis of two
N
‐polyheterocycles indoloazepinobenzimidazole and benzimidazotriazolobenzodiazepine from a common
N
1
‐alkyne‐1,2‐diamine building block is described. The approach involves sequential formation of benzimidazole through cyclocondensation and oxidation, which is followed by the formation of either an azepine ring (through alkyne activation and 6‐
endo‐dig
cyclization, 1,2‐migration with ring expansion, and re‐aromatization), or diazepine and triazole rings through 1,3‐dipolar cycloaddition.