RESUMO
With the increasing relevance of organophosphorus fluorine compounds in the pharmaceutical industry, their synthesis has attracted great attention. Herein, we report an efficient fluorination strategy for P(O)-H and P(O)-OH compounds using sulfuryl fluoride as the fluorination reagent. Avoiding the use of expensive or complex prepreparation reagents for fluoridation, this strategy could conveniently construct a variety of fluorophosphonates and phosphonofluoridates under mild conditions and without additional oxidants.
RESUMO
An efficient and direct ruthenium-catalyzed regioselective hydroxymethylation of (hetero)arenes via C-H activation with paraformaldehyde as a hydroxymethylating reagent is described. The corresponding products can be obtained in good to excellent yield. A number of aryl aldehydes can also be used in place of paraformaldehyde giving the desired alcohol products with similarly good results.
RESUMO
The title compound, (C(6)H(14)N(2))[Cr(3)O(10)], consists of a diazabicyclo[2.2.2]octane-1,4-diium cation and a discrete trichromate anion linked by an N-H.O hydrogen bond. Three CrO(4) tetrahedra are joined via shared O atoms to form the trichromate anion. Supramolecular rings, which can be described by the graph-set motif R(4)(4)(26), are built via N-H.O hydrogen bonds, and C-H.O interactions play lesser roles in forming the structure.