Study on disulfur-backboned nucleic acids:Part Ⅳ.Efficient synthesis of 3',5'-dithio-2'-deoxyguanosine

Pei Hua Shang Chang Mei Cheng Hua Wang Hong Chao Zheng Yu Fen Zhao

引用本文: Pei Hua Shang,  Chang Mei Cheng,  Hua Wang,  Hong Chao Zheng,  Yu Fen Zhao. Study on disulfur-backboned nucleic acids:Part Ⅳ.Efficient synthesis of 3',5'-dithio-2'-deoxyguanosine[J]. Chinese Chemical Letters, 2010, 21(2): 131-134. doi: 10.1016/j.cclet.2009.10.017 shu
Citation:  Pei Hua Shang,  Chang Mei Cheng,  Hua Wang,  Hong Chao Zheng,  Yu Fen Zhao. Study on disulfur-backboned nucleic acids:Part Ⅳ.Efficient synthesis of 3',5'-dithio-2'-deoxyguanosine[J]. Chinese Chemical Letters, 2010, 21(2): 131-134. doi: 10.1016/j.cclet.2009.10.017 shu

Study on disulfur-backboned nucleic acids:Part Ⅳ.Efficient synthesis of 3',5'-dithio-2'-deoxyguanosine

  • 基金项目:

    This work was supported by the National Natural Science Foundation of China (No. 20872078) and the Basic Science Research Foundation of Tsinghua University (No. JC 2001046).

摘要: An efficient and novel method for synthesizing 3',5'-dithio-2'-deoxyguanosine was described.In this method normal guanosine was used as the starting material.A very efficient procedure was used to synthesize 2'-O-tosyiguanosine 1,which used 0.1 eq.DBTO instead of 2 eq.1 was treated with LTBH to give 9-(2-deoxy-β-D-threo-pentofuranosyl)guanine 2.2 could be easily turned to the target compound.

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  • 收稿日期:  2009-05-21
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