98527-15-2Relevant academic research and scientific papers
A new method for halogenation of aromatic compounds by using dimethyldioxirane and tetrabutylammonium halides
Lee, Yean-Jang,Wu, Huan-Ting,Lin, Chia-Ning
experimental part, p. 585 - 587 (2010/04/23)
In this presentation the novel regioselective halogenation of arenes or phenols with dimethyldioxirane and Bu4NX is described. The results showed that a new, versatile and mild method can be utilized for preparation of aryl halides starting with arenes or phenols. Finally, this aryl halide forming methodology is applicable to structurally more complex flavonoids.
Potential neuroleptic agents. 4. Chemistry, behavioral pharmacology, and inhibition of [3H]spiperone binding of 3,5-disubstituted N-[(1-ethyl-2-pyrrolidinyl)methyl]-6-methoxysalicylamides
de Paulis,Kumar,Johansson,Raemsby,Hall,Saellemark,Angeby-Moeller,Ogren
, p. 61 - 69 (2007/10/02)
A series of 3,5-disubstituted N-[(1-ethyl-2-pyrrolidinyl)methyl]-6-methoxysalicylamides was synthesized, starting from the 2,6-dimethoxybenzoic acids, by boron tribromide demethylation of the corresponding 3,5-disubstituted 2,6-dimethoxybenzamides and sep
