Hungerford Natasha L, McKinney Andrew R, Stenhouse Allen M, McLeod Malcolm D
School of Chemistry, F11, The University of Sydney, NSW 2006, Australia.
Org Biomol Chem. 2006 Nov 7;4(21):3951-9. doi: 10.1039/b610499a. Epub 2006 Sep 22.
The temporary protection of 17alpha-alkyl-5alpha-androstane-3beta,16beta,17beta triols as boronate esters is an efficient method for their regioselective functionalisation. This has been applied to the synthesis of protein-steroid conjugates 7-10 suitable for the development of immunoassays targeting classes of steroids banned from competition in Australian horse racing and other sports. The synthesis of steroids sulfate conjugates 42 and 44 for use as reference standards is also reported.
将17α-烷基-5α-雄甾烷-3β,16β,17β-三醇临时保护为硼酸酯是对其进行区域选择性官能化的有效方法。这已应用于蛋白质-类固醇缀合物7-10的合成,这些缀合物适用于开发针对澳大利亚赛马和其他体育赛事中被禁止参赛的类固醇类别的免疫测定。还报道了用作参考标准品的类固醇硫酸酯缀合物42和44的合成。