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Organothiosilanes in the synthesis of functionalized benzothiophenes and benzofurans

Fluoride-ion-induced reactivity of bromo(phenylthio)methyltrimethylsilane with o-hydroxy benzaldehyde and o-mercaptobenzyl alcohol afforded direct and simple access to 2,3-dihydro-2-phenylthio-3-hydroxybenzofuran and 2-phenylthio-3-hydroxy-2,3-dihydrobenzothiophene, respectively. 2-Phenoxy-3-hydroxy...

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Published in:Journal of sulfur chemistry 2009-08, Vol.30 (3-4), p.319-326
Main Authors: Capperucci, Antonella, Degl'Innocenti, Alessandro, Nocentini, Tiziano, Pollicino, Salvatore
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description Fluoride-ion-induced reactivity of bromo(phenylthio)methyltrimethylsilane with o-hydroxy benzaldehyde and o-mercaptobenzyl alcohol afforded direct and simple access to 2,3-dihydro-2-phenylthio-3-hydroxybenzofuran and 2-phenylthio-3-hydroxy-2,3-dihydrobenzothiophene, respectively. 2-Phenoxy-3-hydroxy-2,3-dihydrobenzo-thiophene could be similarly obtained through a slightly modified procedure.
doi_str_mv 10.1080/17415990902998587
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source Taylor and Francis Science and Technology Collection
subjects 2,3-dihydrobenzofuran
2,3-dihydrobenzothiophene
fluoride ion
organothiosilanes
title Organothiosilanes in the synthesis of functionalized benzothiophenes and benzofurans
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