𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Tetraols as Templates for the Synthesis of Large endo-Functionalized Macrocycles

✍ Scribed by Dennis Stoltenberg; Sonja Lüthje; Ole Winkelmann; Christian Näther; Ulrich Lüning


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
537 KB
Volume
2011
Category
Article
ISSN
1434-193X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Observations on Dibutylstannylene as Tem
✍ Bredenkamp, Martin W. ;Flowers, Harold M. ;Holzapfel, Cedric W. 📂 Article 📅 1992 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 863 KB

Macrocyclization / Stannylene template / Template synthesis Dibutylstannylene-mediated macrolactonization of methyl chloride yields polyesters only, a byproduct in all these re-4,6-O-benzylidene-a-~-glucopyranoside (2) with glutaryl and actions. The mechanism of stannylene-mediated macrolacphthaloyl

Synthesis of Branched Oligonucleotides a
✍ Marta G. Grimau; Daniela Iacopino; Anna Aviñó; Beatriz G. de la Torre; Andrea On 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 German ⚖ 212 KB 👁 1 views

## Abstract Branched oligonucleotides with symmetric arms **6**–**15**, which may contain biotin as a second recognition code, were prepared. These molecules are designed to be used for the directed assembly of nanomaterials. The branched structure of the desired oligonucleotides was confirmed by m