Ayres B E, Newall C E, Phillipps G H
Steroids. 1975 Aug;26(2):219-25. doi: 10.1016/s0039-128x(75)80022-5.
3alpha-Hydroxy-5alpha-pregnane-11,20-dione-[21-14C] and 3alpha,21-dihydroxy-5alpha-pregnane-11,20-dione-[21-14C] 21-acetate were prepared from a common radio-labelled intermediate, 21-diazo-3alpha-hydroxy-5alpha-pregnane-11,20-dione-[21-14C] 3-nitrate, obtained by the reaction of 17beta-chlorocarbonyl-3alpha-hydroxy-5alpha-androstan-11-one 3-nitrate with diazomethane-[14C].
3α-羟基-5α-孕烷-11,20-二酮-[21-¹⁴C]和3α,21-二羟基-5α-孕烷-11,20-二酮-[21-¹⁴C] 21-乙酸酯由一种共同的放射性标记中间体21-重氮-3α-羟基-5α-孕烷-11,20-二酮-[21-¹⁴C] 3-硝酸盐制备而成,该中间体通过17β-氯羰基-3α-羟基-5α-雄甾烷-11-酮3-硝酸盐与重氮甲烷-[¹⁴C]反应获得。