首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 0 毫秒
1.
2.
3.
4.
5.
6.
Conclusions A method for the synthesis of 3(2)-O-aminoacylnucleoside 5-di- and triphosphates has been developed which is based on the condensation of the imidazolides of N-tert-butoxycarbonylamino acids with nucleoside di-and triphosphates and subsequent removal of the tert-butoxycarbonyl protection by treatment with hydrogen chloride in absolute ether.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1084–1087, May, 1968.  相似文献   

7.
8.
9.
10.
11.
Conclusions A new method was developed for the synthesis of 3(2)-O-(amino-acyl)nucleotides by the condensation of nucleotides with 1-[(t-butoxycarbonylamino)acyl]imidazoles with subsequent removal of the t-butoxycarbonyl protection by treatment with hydrogen chloride in dry ether.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 378–382, February, 1968.  相似文献   

12.
13.
Conclusions The possibility has been shown of extending the method of synthesis of O-aminoacyl derivatives of nucleotides and nucleoside triphosphates to prepare 3(2)-O-peptidyI-micleoside-5-triphosphates.TranslatedfromlzvestiyaAkademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1369–1372, June, 1970.  相似文献   

14.
15.
16.
17.
18.
Uracil nucleosides and nucleotides undergo a palladium catalyzed coupling reaction with styrenes to yield the respective 5-substituted derivatives.  相似文献   

19.
20.
Summary The thin-layer chromatography of nucleoside and nucleotide derivatives on cellulose has been carried out, and R f values and conditions for the separation and quantitative analysis of these mixtures by this method have been given.Khimiya Frirodnykh Soedinenii, Vol. 1, No. 5, pp. 335–342, 1965  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号