C−H Bond Functionalization in the Synthesis of Fused 1,2,3-Triazoles

A highly modular approach to fused 1,2,3-triazoles has been developed featuring a one-pot procedure combining copper(I) catalyzed azide−alkyne cycloaddition and palladium-catalyzed C−H bond functionalization. A class of structurally unique heterocycles was synthesized in good yields.

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Veröffentlicht in:Organic letters 2010-11, Vol.12 (22), p.5092-5095
Hauptverfasser: Panteleev, Jane, Geyer, Karolin, Aguilar-Aguilar, Angelica, Wang, Letian, Lautens, Mark
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container_end_page 5095
container_issue 22
container_start_page 5092
container_title Organic letters
container_volume 12
creator Panteleev, Jane
Geyer, Karolin
Aguilar-Aguilar, Angelica
Wang, Letian
Lautens, Mark
description A highly modular approach to fused 1,2,3-triazoles has been developed featuring a one-pot procedure combining copper(I) catalyzed azide−alkyne cycloaddition and palladium-catalyzed C−H bond functionalization. A class of structurally unique heterocycles was synthesized in good yields.
doi_str_mv 10.1021/ol102342y
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subjects Alkynes - chemistry
Azides - chemistry
Catalysis
Combinatorial Chemistry Techniques
Copper - chemistry
Cyclization
Heterocyclic Compounds, 4 or More Rings - chemical synthesis
Heterocyclic Compounds, 4 or More Rings - chemistry
Molecular Structure
Palladium - chemistry
Triazoles - chemical synthesis
Triazoles - chemistry
title C−H Bond Functionalization in the Synthesis of Fused 1,2,3-Triazoles
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