Sodium trimethyl silanoate. A hydroxyl synthon for fluoride S(n)Ar type displacements from anthracene-9,10-diones, benz[g]isoquinoline-5-10-diones and nitrobenzenes

Article abstract of DOI:10.1080/00397919808004449

Treatment of fluoroanthracene-9,10-diones, fluorobenz[g]isoquinoline- 5,10-diones and 1- or 4-fluoronitrobenzenes with sodium trimethylsilanoate in THF followed by acidification readily yields the corresponding hydroxyl analogues.

Full text of DOI:10.1080/00397919808004449

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Sodium Trimethyl Silanoate.
A Hydroxyl Synthon
for Fluoride SNAr Type
Displacements from
Anthracene-9,10-diones,
Benz[g]isoquinoline-5–10-
diones and Nitrobenzenes
A. Paul Krapcho a & D. Waterhouse a
a Department of Chemistry , The University of
Vermont , Burlington, VT, 05405, USA
Published online: 22 Aug 2006.
To cite this article: A. Paul Krapcho & D. Waterhouse (1998) Sodium Trimethyl
Silanoate. A Hydroxyl Synthon for Fluoride SNAr Type Displacements from
Anthracene-9,10-diones, Benz[g]isoquinoline-5–10-diones and Nitrobenzenes,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 28:18, 3415-3422, DOI: 10.1080/00397919808004449
To link to this article: http://dx.doi.org/10.1080/00397919808004449
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