scholarly journals Rapid 18F-labeling via Pd-catalyzed S-arylation in aqueous medium

2021 ◽  
Vol 57 (29) ◽  
pp. 3547-3550
Author(s):  
Swen Humpert ◽  
Mohamed A. Omrane ◽  
Elizaveta A. Urusova ◽  
Lothar Gremer ◽  
Dieter Willbold ◽  
...  

Rapid Pd-catalyzed S-arylation with easily accessible 2-[18F]fluoro-5-iodopyridine enables facile preparation of radiolabeled peptides and proteins.


ChemInform ◽  
2010 ◽  
Vol 30 (26) ◽  
pp. no-no
Author(s):  
Agatha Bastida ◽  
Roberto Fernandez-Lafuente ◽  
Gloria Fernandez-Lorente ◽  
Jose M. Guisan ◽  
Giuseppe Pagani ◽  
...  


2016 ◽  
Vol 188 ◽  
pp. 378-384 ◽  
Author(s):  
Thi Xuan Huong Le ◽  
Christophe Charmette ◽  
Mikhael Bechelany ◽  
Marc Cretin


1999 ◽  
Vol 9 (4) ◽  
pp. 633-636 ◽  
Author(s):  
Agatha Bastida ◽  
Roberto Fernández-Lafuente ◽  
Gloria Fernández-Lorente ◽  
JoséM. Guisán ◽  
Giuseppe Pagani ◽  
...  


2005 ◽  
Vol 123 ◽  
pp. 341-344
Author(s):  
A. Khaldoun ◽  
F. González-Caballero ◽  
J. G. López-Durán ◽  
N. Mahrach ◽  
M. L. Kerkeb


TAPPI Journal ◽  
2015 ◽  
Vol 14 (3) ◽  
pp. 167-174 ◽  
Author(s):  
QIANQIAN WANG ◽  
J.Y. ZHU

Mixed office paper (MOP) pulp without deinking with an ash content of 18.1 ± 1.5% was used as raw material to produce nanofiller-paper. The MOP pulp with filler was mechanically fibrillated using a laboratory stone grinder. Scanning electron microscope imaging revealed that the ground filler particles were wrapped by cellulose nanofibrils (CNFs), which substantially improved the incorporation of filler into the CNF matrix. Sheets made of this CNF matrix were densified due to improved bonding. Specific tensile strength and modulus of the nanofiller-paper with 60-min grinding reached 48.4 kN·m/kg and 8.1 MN·m/kg, respectively, approximately 250% and 200% of the respective values of the paper made of unground MOP pulp. Mechanical grinding duration did not affect the thermal stability of the nanofiller-paper.



2017 ◽  
Vol 39 (1) ◽  
pp. 46-52
Author(s):  
T. SAVCHENKO ◽  
◽  
A. GRECHANOVSKY ◽  
A. BRIK ◽  
N. DUDCHENKO


Author(s):  
Dorian Bader ◽  
Johannes Fröhlich ◽  
Paul Kautny

The facile preparation of three regioisomeric thienopyrrolocarbazoles applying a convenient C-H activation approach is presented. Derived from indolo[3,2,1-<i>jk</i>]carbazole, the incorporation of thiophene into the triarylamine framework significantly impacted the molecular properties of the parent scaffold. The developed thienopyrrolocarbazoles enrich the family of triarylamine donors and constitute a novel building block for functional organic materials.



2019 ◽  
Author(s):  
Dorian Bader ◽  
Johannes Fröhlich ◽  
Paul Kautny

The facile preparation of three regioisomeric thienopyrrolocarbazoles applying a convenient C-H activation approach is presented. Derived from indolo[3,2,1-<i>jk</i>]carbazole, the incorporation of thiophene into the triarylamine framework significantly impacted the molecular properties of the parent scaffold. The developed thienopyrrolocarbazoles enrich the family of triarylamine donors and constitute a novel building block for functional organic materials.



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