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1)  16R-bromopregnane-3S
16R-溴代孕甾-3S
1.
The reaction of 16R-bromopregnane-3S,20S-diol diacetate with bases was investigated according to the demand of rationally utilizing steroidal sapogenins.
为了合理利用甾体皂甙元资源,系统地考察了16R-溴代孕甾-3S,20S-二醇二乙酸酯在不同反应条件下与碱的反应。
2.
16R-bromopregnane-3S, 20S-diol diacetate can been easily prepared in a large scale by the transformation of tigogenin obtained from the industrial waste.
<正>16R-溴代孕甾-3S,20S-二醇二乙酸酯可以方便地、大量地从我国制麻工业副产物剑麻皂甙元进行制备,如何利用其合成甾体药物和具有生物活性的天然甾体化合物对于合理利用剑麻皂甙元资
3.
The synthetic key step involved a new fragmentation reaction of 16R-bromopregnane-3S, 20S-diol recently found by us.
本文利用我们最近发现的16R-溴代孕甾-3S,20S-二醇的碎裂反应,从剑麻皂甙元降解产物—孕甾三醇出发
2)  pregnane-3S
孕甾-3S
1.
In order to make rational utilization of tigogenin, the reaction of pregnane-3S,16S,20S-triol and HBr/HOAc was explored in detail, and a regioselective acetylation-bromination reaction of preg- nane-3S,16S,20S-triol was found during this exploration.
为合理利用剑麻皂甙元资源,系统地考察了孕甾-3S,16S,20S-三醇和溴化氢/乙酸溶液的反应,并且发现了孕甾-3S,16S,20S-三醇的区域选择性乙酰化溴代反应,从而为转化孕甾-3S,16S,20S-三醇成为16R-溴代孕甾-3S,20S-二醇二乙酸酯提供了一个有效方法。
3)  pregn-16-ene-3S
孕甾-16-烯-3S
1.
The efficient synthesis of pregn-16-ene-3S,20S-diol diacetate and the restudy of its Pd-catalyzed reaction
孕甾-16-烯-3S,20S-二醇二乙酸酯的高效合成及其钯催化反应的再研究
2.
Some useful and controllable reaction results were obtained through such investigation, in which, 16R-bromopregnane-3S,20S-diol diacetate was chemo-selec-tively converted into pregn-16-ene-3S,20S-diol diacetate, 16R-bromopregnane-3S,20S-diol, preg-nane-3S,16S,20S-triol, pregne-14,16-dien-3S-ol acetate and androst-16-en-3S-ol respectively.
给出了选择性地分别转化16R-溴代孕甾-3S,20S-二醇二乙酸酯成为孕甾-16-烯-3S,20S-二醇二乙酸酯、16R-溴代孕甾-3S,20S-二醇、孕甾-3S,16S,20S-三醇、孕甾-14,16-二烯-3S-醇乙酸酯和雄甾-16-烯-3S-醇等化合物的可控性反应结果。
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4)  Pregnene
孕甾
1.
Synthesis and Spectral Analysis of Three Kinds of Epoxy Pregnene Derivatives;
三种环氧孕甾衍生物的合成和光谱特性研究
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5)  an-drost-16-en-3S-ol
雄甾-16-烯-3S-醇
6)  16β-Bromopregna-4,9(11)-dien-17α-ol-3,20-dione
16β-溴-17α-羟基孕甾-4,9(11)-二烯-3,20-二酮
补充资料：来代
1.后代;后世。
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