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Volumn 54, Issue 37, 2015, Pages 10912-10916

Palladium-Catalyzed Dearomative Cyclocarbonylation by C-N Bond Activation

Author keywords

C N activation; cyclocarbonylation; dearomatization; palladium; quinolizinones

Indexed keywords

CATALYSIS; CHEMICAL ACTIVATION; PALLADIUM;

EID: 84940719878     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201504805     Document Type: Article
Times cited : (70)

References (69)
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    • See the Supporting Information for details. CCDC 1401870 (2 o), 1401869 (2q), 1401936 (2w), and 1401871 ([Pd(Xantphos)I2]) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre.
    • See the Supporting Information for details. CCDC 1401870 (2 o), 1401869 (2q), 1401936 (2w), and 1401871 ([Pd(Xantphos)I2]) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre.
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    • Control experiments showed that N,N-diisopropyl-4-(pyridin-2-yl)but-3-enamide cannot be converted into the desired product 2 a in the presence of base and the Pd catalyst at 120 C. This result supports the proposed mechanism shown in Figure 2 (see the Supporting Information for details).
    • Control experiments showed that N,N-diisopropyl-4-(pyridin-2-yl)but-3-enamide cannot be converted into the desired product 2 a in the presence of base and the Pd catalyst at 120 C. This result supports the proposed mechanism shown in Figure 2 (see the Supporting Information for details).


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