## 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
✦ 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
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
ChemInform Abstract: Nucleotides. Part 5
✍
T. WAGNER; W. PFLEIDERER
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 32 KB
👁 1 views