Kuivila, Henry G. published the artcileElimination and substitution in the reactions of vicinal dihalides and oxyhalides trimethylstanoylsodium. Effects of solvent and of ion aggregation on course and stereochemistry, HPLC of Formula: 594-81-0, the publication is Journal of Organic Chemistry (1979), 44(26), 4774-81, database is CAplus.
Vicinal dihalides react with Me3SNa via anti stereochem. to produce the corresponding alkenes in nearly quant. yields; MeOCHMeCHBrMe yields both elimination and substitution (MeOCHMeCHMeSnMe3) products. The stereochem. is predominantly syn when THF is the solvent, and elimination predominates. When tetraglyme is the solvent, substitution is the predominant reaction; the stereochem. of both substitution and elimination is nonspecific. The mechanistic implications of these observations are considered.
Journal of Organic Chemistry published new progress about 594-81-0. 594-81-0 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 2,3-Dibromo-2,3-dimethylbutane, and the molecular formula is C6H12Br2, HPLC of Formula: 594-81-0.
Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary