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Hydrodehalogenation of Aryl Chlorides and Aryl Bromides Using a Microwave-Assisted, Copper-Catalyzed Concurrent Tandem Catalysis Methodology

https://doi.org/10.1021/om2003706

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1521-3773(20021115)41:22<4176::aid-anie4176>3.0.co;2-uopenalex-snapshot

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inferredcites →https://doi.org/10.1002/anie.200400655openalex-snapshot

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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trans ‐ N 1 , N 2 ‐Dimethyl‐1,2‐Cyclohexanediamine

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