Lansbergen Beatrice, Meister Catherine S, McLeod Michael C
Bayer AG, Research & Development Crop Science, Industriepark Höchst, 65926 Frankfurt, Germany.
Beilstein J Org Chem. 2021 Feb 10;17:404-409. doi: 10.3762/bjoc.17.36. eCollection 2021.
A novel reactivity of 1,1,1-trifluoroalkanones is reported, where the reaction with AlCl results in the formation of 1,1-dichloro-1-alkenones. The reaction scope was found to be broad, with various chain lengths and aryl substituents tolerated. For substrates containing an electron-rich aromatic ring, further reactions take place, resulting in bicyclic and/or rearrangement products.
据报道,1,1,1-三氟代烷酮具有一种新的反应活性,即它与氯化铝反应会生成1,1-二氯-1-烯酮。研究发现该反应的适用范围很广,能耐受各种链长和芳基取代基。对于含有富电子芳环的底物,会发生进一步反应,生成双环和/或重排产物。