Allylic selenides in organic synthesis: new methods for the synthesis of allylic amines was written by Shea, Regan G.;Fitzner, Jeffrey N.;Fankhauser, John E.;Spaltenstein, Andreas;Carpino, Philip A.;Peevey, Richard M.;Pratt, Daniel V.;Tenge, Bradley J.;Hopkins, Paul B.. And the article was included in Journal of Organic Chemistry in 1986.HPLC of Formula: 28322-40-9 This article mentions the following:
Oxidative rearrangement of allylic selenides in the presence of various amine nucleophiles provides synthetic access to a variety of allylic amine derivatives The stereochem. outcome of these reactions has been investigated, and is consistent with a [2,3]-sigmatropic rearrangement mechanism. Several
Isopentyltriphenylphosphonium bromide (cas: 28322-40-9) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.HPLC of Formula: 28322-40-9
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary