Baldwin, Jack E. published the artcile5-Isothiazolidinonyl and 5-isoxazolidinonyl radicals. Approaches to the biogenetic-type synthesis of β-lactams, SDS of cas: 18791-02-1, the publication is Tetrahedron (1981), 37(11), 2181-9, database is CAplus.
A possible mechanism for penicillin biosynthesis involves the rearrangement of a 5-isothiazolidinonyl radical I [R = NHCO(CH2)3CH(N+H3)CO2–, R1 = H, R2 = CH(CO2H)CHMe2] to a β-lactam. However, the model radicals I (R = R1 = Ph, R2 = CMe3; R = Br3C, R1 = H, R2 = CMe3), generated in the conversion of II (R = Br, R1 = R2 = Ph) to II (R = H, R1, R2 as before) and II (RR1 = bond, R2 = H) to II (RR1 = bond, R2 = Br3C), resp., failed to give β-lactams. The analogous reaction of a 5-isoxazolidinonyl radical is the basis for a potential synthesis of clavulanic acid, but again the rearrangement was not observed in the model radical III (R = H, R1 = absent) generated in the conversion of III (R = H, R1 = CO2OCMe3) to III (RR1 = bond).
Tetrahedron 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 C3H3Br2ClO, SDS of cas: 18791-02-1.
Referemce:
https://en.wikipedia.org/wiki/Chloride,
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