𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Nucleotides. Part 73. Oligoribonucleotide Synthesis with the (2-Cyano-1-phenylethoxy)carbonyl (2c1peoc) Group for the 5′-Hydroxy Protection.

✍ Scribed by Ursula Muench; Wolfgang Pfleiderer


Publisher
John Wiley and Sons
Year
2003
Weight
52 KB
Volume
34
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Nucleotides. Part LXXIII : Oligoribonucl
✍ Ursula Münch; Wolfgang Pfleiderer 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 German ⚖ 292 KB

## Abstract The (2‐cyano‐1‐phenylethoxy)carbonyl (2c1peoc) group was developed as a new base‐labile protecting group for the 5′‐OH function in solid‐phase synthesis of oligoribonucleotides __via__ the phosphoramidite approach. The half‐lives of its __β__‐elimination process by 0.1M DBU (1,8‐diazabi

Nucleotides. Part XLI. The 2-dansylethox
✍ Frank Bergmann; Wolfgang Pfleiderer 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 German ⚖ 896 KB

Use of the 2-dansylethoxycarbonyl (= 2-{[5-(dimethylan1ino)naphthalen-I-yl]sulfonyl}ethoxycarbonyl; Dnseoc) group as an intermediate 5'-OH protecting group in oligodeoxyribonucleotide synthesis using the automated phosphoramidite approach is described in a model study to an alternative strategy in R