Abstract
A range of halogenated methylthiophenes undergo dehalogenative condensation upon FVP over magnesium or calcium to give products including benzodithiophenes; in some cases this involves a novel rearrangement by equilibration of alkenylthienyl radicals via thiophene-fused cyclopropylmethyl intermediates.
Original language | English |
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Pages (from-to) | 19379-19381 |
Number of pages | 3 |
Journal | RSC Advances |
Volume | 5 |
Issue number | 25 |
Early online date | 9 Feb 2015 |
DOIs | |
Publication status | Published - 17 Feb 2015 |