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A Mukaiyama-Claisen Approach to 3,5-Diketo Esters

Synlett (2015) 26(11) 1525-1527
DOI: 10.1055/s-0034-1380145
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Abstract

A thermally promoted synthesis of 3,5-diketo esters via a Mukaiyama-Claisen reaction of 4H-1,3-dioxin-4-one derivatives with silyl enolates has been developed. The desired oligocarbonyl compounds were obtained with moderate to good yields.

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Wang, Q., & List, B. (2015). A Mukaiyama-Claisen Approach to 3,5-Diketo Esters. Synlett, 26(11), 1525–1527. https://doi.org/10.1055/s-0034-1380145

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