3,4-Alkylenedioxy ring formation via double Mitsunobu reactions: an efficient route for the synthesis of 3,4-ethylenedioxythiophene (EDOT) and 3,4-propylenedioxythiophene (ProDOT) derivatives as monomers for electron-rich conducting polymers
- 26 September 2002
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 21,p. 2498-2499
- https://doi.org/10.1039/b205907j
Abstract
3,4-Alkylenedioxy ring functionalized thiophenes (XDOT’s) have been synthesized by double Mitsunobu reactions to yield precursors to monomers for conjugated and electrically conducting polymers, including the commercially important 3,4-ethylenedioxythiophene (EDOT).Keywords
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