Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 35, Pages 5245-5247Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b912022j
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Funding
- JSPS [19390001]
- MEXT, Japan [19028001, 20037002]
- Novartis Foundation (Japan) for the Promotion of Science
- Uehara Memorial Foundation
- Akiyama Foundation
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A transition metal-catalyzed [2 + 2 + 2] cycloaddition between alpha,omega-diynes and 3,4-pyridynes has been realized for the first time, producing isoquinolines in good yields by using a nickel(0) catalyst.
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