Mohamed Nadia R, Elmegeed Gamal A, Abd-ElMalek Hoda A, Younis Magdi
Photochemistry Department, National Research Centre, Dokki, Giza, Egypt.
Steroids. 2005 Mar;70(3):131-6. doi: 10.1016/j.steroids.2004.11.001.
Steroid derivatives V, VI, VII and VIII reacted with Lawesson's reagent (LR) to produce spiro-oxazaphosphole-4',17-androstene derivative XI, diazaphospholoandrostane XIV and the thionated derivatives XVI and XVII, respectively. The structures of the new compounds were confirmed by analytical and spectroscopic evidence. A mechanism accounting for the formation of the new compounds was given. The in vitro antimicrobial activity of the new compounds were tested.
甾体衍生物V、VI、VII和VIII与劳森试剂(LR)反应,分别生成螺-恶唑磷环-4',17-雄甾烯衍生物XI、二氮杂磷环雄甾烷XIV以及硫代衍生物XVI和XVII。通过分析和光谱证据证实了新化合物的结构。给出了新化合物形成的反应机理。测试了新化合物的体外抗菌活性。