4.8 Article

A Highly Tunable Stereoselective Dimerization of Methyl Ketone: Efficient Synthesis of E- and Z-1,4-Enediones

Journal

ORGANIC LETTERS
Volume 15, Issue 9, Pages 2148-2151

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol4006344

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Funding

  1. 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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