Abstract
3-Substituted cholesterols and 7-substituted pseudocholesterols undergo a facile photooxygenation sensitized by 9, 10-dicyanoanthracene (DCA) and lumiflavin (LF) to give similar, oppositely-positioned enol derivatives. Both steroids showed the same reaction pattern associated with the endocyclic 5- and 4-olefin units, respectively. The reaction was proposed to proceed via the ene reaction of singlet oxygen and subsequent rearrangement of the initially formed 5α-hydroperoxides.
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Shuping, W., Zhiqin, J., Heting, L., Li, Y., & Daixun, Z. (2001). Sensitized photooxygenation of cholesterol and pseudo-cholesterol derivatives via singlet oxygen. Molecules, 6(1), 52–60. https://doi.org/10.3390/60100052
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