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Search for "1,4-dinitrocompounds" in Full Text gives 1 result(s) in Beilstein Journal of Organic Chemistry.
Cathodic hydrodimerization of nitroolefins
Beilstein J. Org. Chem. 2015, 11, 1163–1174, doi:10.3762/bjoc.11.131
- formation; 1,4-dinitrocompounds; electrosynthesis; nitroalkene; Introduction Olefins being activated by an electron withdrawing group can be hydrodimerized by cathodic reduction [1][2]. Thereby, the cathode serves as cheap, versatile, immobilized and mostly non-polluting reagent providing economical and
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