化学
氚
标签
立体专一性
类固醇
产量(工程)
氘
核磁共振波谱
氯仿
溶剂
放射化学
立体化学
有机化学
生物化学
激素
催化作用
核物理学
物理
冶金
材料科学
量子力学
作者
Carel W. Funke,Frans M. Kasperen,Jan Wallaart,Gerard N. Wagenaars
标识
DOI:10.1002/jlcr.2580200709
摘要
Abstract The 3 H NMR spectra of a series of 7 steroids tritiated at C(1), C(2), C(6), C(7), C(9) and C(16) yield quantitative information on the 3 H distribution in these compounds. Deuterated chloroform is not a good solvent to examine the regio‐ and stereospecificity of the labelling process for acid labile positions such as C(2) in a 3‐oxosteroid and C(6) in a 3‐oxo‐Δ 4 ‐steroid.
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