A novel linker for the generation of alkyl-, acyl-and arylguanidines as an attachment point in solid phase synthesis has been developed. Introduction of a suitably functionalized thiourea to Wang resin via a carbamate linkage, followed by displacement of sulfur with a 1 ° or 2 ° amine affords resin
✦ LIBER ✦
A novel linker for the solid-phase synthesis of a library of 3′-thiophosphorylated dinucleotides
✍ Scribed by Arlène Roland; Yufang Xiao; Yi Jin; Radhakrishnan P Iyer
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 112 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The preparation of a controlled-pore-glass (CPG) support carrying a novel linker is described. This support was compatible with the established phosphoramidite method of solid-phase oligonucleotide synthesis. The use of this linker for the synthesis of a library of 3%-thiophosphorylated dinucleotides is described.
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