Kim, EH Koo, BS Song, CE Lee, KJ 2024-01-21T11:39:00Z 2024-01-21T11:39:00Z 2021-09-05 2001-11 0039-7911 https://pubs.kist.re.kr/handle/201004/140089 Aromatic methyl ketones undergo alpha -halogenation on treatment with sodium halide in the presence of oxone (R) in aqueous methanol. However, electron-rich hetero aromatic methyl ketones afford ring bromination products preferentially. English MARCEL DEKKER INC OXIDATIVE CLEAVAGE PEPTIDE-SYNTHESIS DIOXIRANE CARBONYL Halogenation of aromatic methyl ketones using Oxone (R) and sodium halide Article 10.1081/SCC-100107011 1 SYNTHETIC COMMUNICATIONS, v.31, no.23, pp.3627 - 3632 SYNTHETIC COMMUNICATIONS 31 23 3627 3632 scie scopus 000171792400009 2-s2.0-0034770940 Chemistry, Organic Chemistry Article OXIDATIVE CLEAVAGE PEPTIDE-SYNTHESIS DIOXIRANE CARBONYL halogenation