ArticleBeilstein journal of organic chemistry2024
Germanyl triazoles as a platform for CuAAC diversification and chemoselective orthogonal cross-coupling.
Article in Beilstein journal of organic chemistry, 2024. 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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Who cites it
3 citing papers in PubMed.
- Clicking acylgermanes: modular access to photoinitiators for visible-light photopolymerization.Organic chemistry frontiers : an international journal of organic chemistry · 2026Article
- Discovery of Fused Isoquinolinone/Triazole as a Scaffold for Tankyrase and PARP Inhibition.Journal of medicinal chemistry · 2026Article
- Copper catalysis: a constantly evolving field.Beilstein journal of organic chemistry · 2025Article
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Authors and funding
6 authors.
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Abstract
We report the synthesis of germanyl triazoles formed via a copper-catalysed azide-alkyne cycloaddition (CuAAC) of germanyl alkynes. The reaction is often high yielding, functional group tolerant, and compatible with complex molecules. The installation of the Ge moiety enables further diversification of the triazole products, including chemoselective transition metal-catalysed cross-coupling reactions using bifunctional boryl/germyl species.
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