中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | 2,4,6-trithiaheptane 2,2,6-trioxide | —— | C4H10O3S3 | 202.32 |
Novel silica-induced controlled disproportionation of α-mercaptosulfones produces α-mercapto α′-sulfonyl sulfides. Its discovery and exploitation, as the heart of a new process – vault isomerization – permits the elaboration of a more efficient synthesis of a previously described synthetic precursor.
A new cleavage reaction establishes rational access to the title compound. Treatment of the title compound with molecular chlorine establishes that methylsulfonyl is better than chloro as a directing group in the chlorination of unsymmetrical sulfides