Redox-active tetrathiafulvalene and dithiolene compounds derived from allylic 1,4-diol rearrangement products of disubstituted 1,3-dithiole derivatives
2010 ◽
Vol 6
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pp. 1002-1014
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Keyword(s):
We present a series of compounds by exploiting the unusual 1,4-aryl shift observed for electron-rich 1,3-dithiole-2-thione and tetrathiafulvalene (TTF) derivatives in the presence of perchloric acid. The mechanistic features of this rearrangement are discussed since this synthetic strategy provides an alternative route for the synthesis and functionalisation of sulfur rich compounds including redox active compounds of TTFs, and a Ni dithiolene.
2016 ◽
Vol 292
(1)
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pp. 121-133
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2001 ◽
Vol 31
(11)
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pp. 1287-1312
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Keyword(s):
2015 ◽
Vol 21
(51)
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pp. 18516-18527
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2014 ◽
Vol 58
(8)
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pp. 1739-1749
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2019 ◽
Vol 21
(28)
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pp. 15823-15832
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Keyword(s):
1997 ◽
Vol 7
(7)
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pp. 1227-1236
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2004 ◽
Vol 810
(1)
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pp. 93-100
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