Journal
ORGANOMETALLICS
Volume 35, Issue 10, Pages 1420-1425Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.6b00020
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Funding
- National Basic Research Program of China (973 Program) [2015CB856600]
- National Natural Science Foundation of China [21332009, 21421091]
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Synthesis of ferrocene-based pyridinones via Rh(III)-catalyzed annulation of ferrocenecarboxamides with internal alkynes has been developed using a directing group as the internal oxidant. This method displays good functional group tolerance and delivers ferrocene-based pyridinones generally in moderate to good yields. Additionally, an asymmetric reaction can be achieved in the presence of a chiral catalyst Rh1.
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