Abstract:
:A set of new sulfurizing agents representing disulfides of arylsulfonic acids has been developed for the automated synthesis of phosphorothioate oligonucleotide analogues via the phosphoramidite method. These reagents, such as bis(benzenesulfonyl)disulfide, bis(p-toluenesulfonyl)disulfide, bis(p-methoxybenzensulfonyl)disulfide, and bis (p-chlorobenzenesulfonyl) disulfide, are easily prepared crystalline solid compounds. They are relatively inexpensive, easy to handle, and efficiently convert internucleotide cyanoethyl phosphite to the phosphorothioate triester within 1-2 min. The efficiency of phosphorothioate oligonucleotide synthesis with the use of these reagents is comparable to that of phosphodiester oligonucleotides.
journal_name
Nucleic Acids Resjournal_title
Nucleic acids researchauthors
Efimov VA,Kalinkina AL,Chakhmakhcheva OG,Hill TS,Jayaraman Kdoi
10.1093/nar/23.20.4029subject
Has Abstractpub_date
1995-10-25 00:00:00pages
4029-33issue
20eissn
0305-1048issn
1362-4962pii
5c0142journal_volume
23pub_type
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