68972-94-1Relevant academic research and scientific papers
Synthesis of 3,4-Ethylenedioxythiophene (EDOT) from (Z)-but-2-ene-1,4-diol or but-2-yne-1,4-diol
Hachiya, Iwao,Matsumoto, Tomohiro,Inagaki, Tatsuhiko,Takahashi, Atsushi,Shimizu, Makoto
, p. 449 - 460 (2010)
3,4-Ethylenedioxythiophene (EDOT) was synthesized from commercially available (Z)-but-2-ene-1,4-diol or but-2-yne-1,4-diol using epoxidation, etherification, and thiophene formation. The Japan Institute of Heterocyclic Chemistry.
The synthesis of the 2, 3-difluorobutan-1, 4-diol diastereomers
Szpera, Robert,Kovalenko, Nadia,Natarajan, Kalaiselvi,Paillard, Nina,Linclau, Bruno
supporting information, p. 2883 - 2887 (2018/01/17)
The diastereoselective synthesis of fluorinated building blocks that contain chiral fluorine substituents is of interest. Here we describe optimisation efforts in the synthesis of anti-2, 3-difluorobutane-1, 4-diol, as well as the synthesis of the corresponding syn-diastereomer. Both targets were synthesised using an epoxide opening strategy.
