| Autor: |
Martinelli, Angelo, Nitti, Andrea, Po, Riccardo, Pasini, Dario |
| Zdroj: |
The Journal of Organic Chemistry; March 2024, Vol. 89 Issue: 6 p4237-4243, 7p |
| Abstrakt: |
We present a divergent synthetic approach to C2-symmetrical 3,4-Ethylenedioxythiophene (EDOT) monomers in which functionalities can be introduced as pendant chains from the ethylene bridge. The key synthon, obtained through a high yielding trans-etherification, is the chiral EDOT with bromomethyl pendant groups and is prone to substitution reactions with oxygen-based nucleophiles. Elimination of the key precursor affords a diene that can be elaborated into unprecedented PhEDOT monomers using the Diels–Alder reaction. The strategy is further validated by the synthesis of a dithiane-containing EDOT. |
| Databáze: |
Supplemental Index |
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