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Synthesis 2011(2): 210-212
DOI: 10.1055/s-0030-1258342
DOI: 10.1055/s-0030-1258342
SHORTPAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of Diisothiocyanato-Functionalized 2,2′-Bipyridines
Further Information
Received
15 October 2010
Publication Date:
26 November 2010 (online)
Publication History
Publication Date:
26 November 2010 (online)
Abstract
Three new diisothiocyanato-functionalized 2,2′-bipyridines have been synthesized in four consecutive steps. Starting from 4-amino-2-chloro- and 2-amino-6-bromopyridine, respectively, we first prepared the corresponding diamino-2,2′-bipyridines via homo- or Negishi cross-coupling reactions which were subsequently reacted with thiophosgene.
Key words
bipyridine - isothiocyanates - amines - thiophosgene - cross-coupling reactions
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