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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >PREPARATION OF IODO-INDUCED 1,3-OXATHIANE COMPOUNDS VIA INTRAMOLECULAR PUMMERER REARRANGEMENT OF 2-BENZYLSULFINYL-BICYCLO[2.2.1]HEPT-5-ENE
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PREPARATION OF IODO-INDUCED 1,3-OXATHIANE COMPOUNDS VIA INTRAMOLECULAR PUMMERER REARRANGEMENT OF 2-BENZYLSULFINYL-BICYCLO[2.2.1]HEPT-5-ENE

机译:通过2-苯甲基磺酰基-双环[2.2.1] HEPT-5-ENE的分子内重整来制备碘诱导的1,3-氧杂蒽化合物

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摘要

Iodooxathianes (2a and 2b) were prepared from the #gamma#,#delat#-unsaturated sulfinyl compound (1) via the iodonium-promoted intramolecular Pummerer reaction. A two-step conversion of 1 into 2a and 2b involving iodohydrination and the Pummerer rearrangement was also achieved.
机译:通过γ-,#delat#-不饱和亚磺酰基化合物(1)经碘鎓促进的分子内Pummerer反应制备碘代氧杂蒽(2a和2b)。还实现了1到2a和2b的两步转化,包括碘代水合和Pummerer重排。

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