Takano, Seiichi published the artcileChiral synthesis of both enantiomers of 1,4-dideoxy-1,4-iminolyxitol and 1,4-dideoxy-1,4-iminoribitol, Synthetic Route of 18791-02-1, the publication is Tetrahedron: Asymmetry (1992), 3(6), 681-4, database is CAplus.
Reaction of 2,3-dibromopropionyl chloride with 4-methoxyphenol and (S)-1-methylbenzylamine yielded a 4:5 mixture of readily separable diastereomeric aziridine esters I (R = C6H4OMe-4) in an excellent yield. Thermal intermol. 1,3-dipolar cycloaddition of both diastereomers with vinylene carbonate, furnished four readily separable diastereomeric pyrrolidine esters, resp., which were transformed into both enantiomers of title compounds
Tetrahedron: Asymmetry published new progress about 18791-02-1. 18791-02-1 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is 2,3-Dibromopropionylchloride, and the molecular formula is C14H22O2, Synthetic Route of 18791-02-1.
Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics