ArticleBeilstein journal of organic chemistry2012
Copper-catalyzed CuAAC/intramolecular C-H arylation sequence: Synthesis of annulated 1,2,3-triazoles.
Article in Beilstein journal of organic chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed.
- Photoinduced C-H arylation of 1,3-azolesChemical science · 2024Article
- Concise synthesis ofRSC advances · 2019Article
- Assembly of fully substituted triazolochromenes via a novel multicomponent reaction or mechanochemical synthesis.Beilstein journal of organic chemistry · 2018Article
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3 authors.
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Abstract
Step-economical syntheses of annulated 1,2,3-triazoles were accomplished through copper-catalyzed intramolecular direct arylations in sustainable one-pot reactions. Thus, catalyzed cascade reactions involving [3 + 2]-azide-alkyne cycloadditions (CuAAC) and C-H bond functionalizations provided direct access to fully substituted 1,2,3-triazoles with excellent chemo- and regioselectivities. Likewise, the optimized catalytic system proved applicable to the direct preparation of 1,2-diarylated azoles through a one-pot C-H/N-H arylation reaction.
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