99070-34-5Relevant academic research and scientific papers
Synthesis of purpuroine A, nakirodin A and MDN-0104: The hidden puzzles and risk of error in their configurational assignments
Wu, Wen-Ju,Wu, Yikang,Liu, Bo
, p. 1265 - 1274 (2017)
The unusual (R) configuration previously assigned (with seemingly undoubted evidence) to purpuroin A and nakirodin A was disproved by synthesis. The optical rotation and NMR data for structure assigned for salt-free nakirodin A were made available for the
BROMINATION OF AROMATIC MOLECULES WITH POLYMER SUPPORTED REAGENTS
Zajc, Barbara,Zupan, Marko
, p. 7869 - 7878 (2007/10/02)
Crosslinked co poly/styrene-4-vinyl(N-hexylpyridinium bromide) was converted with bromine or chlorine to insoluble polymer supported complexes 1 or 2 respectively, and their reactivity studied in reactions with various aromatic molecules.Reagent 1 was found in all cases to be milder than reagent 2 and regiospecifically transformed alkoxy and amino substituted benzenes (3) into 4-bromo derivatives, while corresponding reactions with 2 resulted in dibromo derivatives.Several benzoheterocyclic molecules were converted with 1 to substitution or addition products, i.e. 2,3-dibromo-N-methylpyrrole, 3-bromobenzo/b/thiophene, and 2,3-dibromo-2,3-dihydrobenzofuran.In the series of ortho-alkyl disubstituted benzene derivatives, i.e. o-xylene, indane, and tetraline, where the Mills-Nixon effect was established with various electrophilic reagents, bromination reactions with 2 showed higher β-selectivity than the corresponding reactions with bromine.The rate of bromination in various alkyl substituted benzenes with reagent 2 depended on the magnitude of the alkyl group, as well as the para/ortho regioselectivity, amounting to 100percent in the case of tert-butylbenzene.
