Journal
ORGANIC LETTERS
Volume 15, Issue 9, Pages 2148-2151Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol4006344
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Funding
- 973 program [2010CB912103]
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A new method for the tunable synthesis of 1,4-enedione directly from aromatic methyl ketone is described. This tandem reaction enables the construction of symmetric and unsymmetric 1,4-enediones with complete E-selectivity. Moreover, the resulting E-1,4-enedione could be transformed into a Z-isomer by irradiation with 23 W of white light.
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