𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and Properties of Oligonucleotides Carrying Cryptolepine Derivatives

✍ Scribed by Ramon Eritja


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
94 KB
Volume
1
Category
Article
ISSN
1612-1872

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis and Triple-Helix-Stabilization
✍ Anna Aviño; Marta G. Grimau; Miriam Frieden; Ramon Eritja 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 German ⚖ 195 KB

## Abstract The synthesis of several branched oligonucleotides, __i.e.__, of the parallel hairpins **5**–**8** and the Y‐shaped **9** is described, together with their use in the formation of pyrimidine⋅pyrimidine⋅purine triple helices. Special attention was paid to the optimization of the assembly

Cellulose Derivatives Carrying Triphenyl
✍ Jinqing Qu; Wenbo Liao; Huanqin Chen; Toshio Masuda 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 354 KB

## Abstract A novel ethyl cellulose derivative [poly(**1**)] that carries triphenylamine moieties is synthesized with a moderate number‐average molecular weight up to 78 200 in 85% yield by the reaction of 4‐(diphenylamino)benzoic acid with the residual hydroxy group of ethyl cellulose. Poly(**1**)

Synthesis and properties of radiolabeled
✍ S. Wagner; R. Eritja; M. Zuhayra; F. Oberdorfer; A. Mohammed; W. Mier; U. Haberk 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 French ⚖ 140 KB

## Abstract A solid phase technique for the preparation of antisense oligodeoxynucleotides (ODNs) is described featuring 5′‐end conjugated 4‐[(1,4,8,11‐tetraazacyclotet‐radec‐1‐yl)‐methyl]benzoic acid (CPTA). Using Fmoc‐protected CPTA–C6 amidite, CPTA was conjugated to ODNs at the end of an automat

Synthesis of Oligonucleotides Carrying A
✍ Beatriz G. de la Torre; Juan Carlos Morales; Anna Aviñó; Daniela Iacopino; Andre 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 German ⚖ 194 KB 👁 1 views

## Dedicated to Prof. Dr. Wolfgang Pfleiderer on the occasion of his 75th birthday Oligodeoxynucleotide conjugates 1 ± 15 carrying anchoring groups such as amino, thiol, pyrrole, and carboxy groups were prepared. A post-synthetic modification protocol was developed. In this method 2'-deoxy-O 4 -(p