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Issue 13, 2007
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Formation of stable enols from 1,4-dilithio-1,3-dienes and acid chlorides by a de-aromatization/Michael addition/re-aromatization domino process

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Abstract

Stable enols were synthesized from the reaction of (1Z,3Z)-1,4-dilithio-1,3-dienes with acid chlorides and structurally characterized by single-crystal X-ray analysis. These stable enols were formed by a novel de-aromatization/Michael addition/re-aromatization domino process.

Graphical abstract: Formation of stable enols from 1,4-dilithio-1,3-dienes and acid chlorides by a de-aromatization/Michael addition/re-aromatization domino process

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Publication details

The article was received on 04 Apr 2007, accepted on 18 May 2007 and first published on 31 May 2007


Article type: Paper
DOI: 10.1039/B705110G
Citation: Org. Biomol. Chem., 2007,5, 2114-2118

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    Formation of stable enols from 1,4-dilithio-1,3-dienes and acid chlorides by a de-aromatization/Michael addition/re-aromatization domino process

    Q. Hu, C. Wang, D. Li and Z. Xi, Org. Biomol. Chem., 2007, 5, 2114
    DOI: 10.1039/B705110G

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