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Issue 15, 2004
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Intramolecular C–H insertions adjacent to sulfur for the diastereoselective synthesis of thienofuranones

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Abstract

A new approach to the diastereoselective synthesis of thienofuranones is described in which an intramolecular 1,5-carbenoid C–H insertion adjacent to sulfur features as a key step.

Graphical abstract: Intramolecular C–H insertions adjacent to sulfur for the diastereoselective synthesis of thienofuranones

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Publication details

The article was received on 20 Feb 2004, accepted on 26 May 2004 and first published on 30 Jun 2004


Article type: Communication
DOI: 10.1039/B402603A
Citation: Chem. Commun., 2004, 1772-1773
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    Intramolecular C–H insertions adjacent to sulfur for the diastereoselective synthesis of thienofuranones

    P. S. Skerry, N. A. Swain, D. C. Harrowven, D. Smyth, G. Bruton and R. C. D. Brown, Chem. Commun., 2004, 1772
    DOI: 10.1039/B402603A

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