Tetrathiomolybdate Mediated Rearrangement of Aziridinemethanol Tosylates: A Thia-Aza-Payne Rearrangement
作者:Devarajulu Sureshkumar、Srinivasamurthy Koutha、Venkataraman Ganesh、Srinivasan Chandrasekaran
DOI:10.1021/jo100640w
日期:2010.8.20
Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as the major product and cyclic disulfides as minor product under mild reaction conditions via an unprecedented thia-aza-Payne-type rearrangement. Interestingly, when the reaction of 1 was carried out with 2-aziridino-cyclohexanol derivatives it resulted in the formation of thia-bicyclo[3.1.1]heptane or
氮丙啶甲醇磺酸酯与四
硫代
钼酸盐1反应,在温和的反应条件下,通过空前的
硫杂-氮杂-佩因类型的重排,以
硫杂
环丁烷衍
生物为主要产物,环状二
硫键为次要产物。有趣的是,当1与2-
叠氮基-
环己醇衍
生物进行反应时,会导致生成噻二环[3.1.1]
庚烷或二
硫二环[3.2.1]
辛烷衍
生物。