solid phase chemistry
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2018 ◽  
Vol 46 (14) ◽  
pp. 6996-7005 ◽  
Author(s):  
Erin E Duffy ◽  
Daniele Canzio ◽  
Tom Maniatis ◽  
Matthew D Simon

Synthesis ◽  
2018 ◽  
Vol 50 (06) ◽  
pp. 1199-1208 ◽  
Author(s):  
Jan Hlaváč ◽  
Kristýna Bürglová

Trimethylsilanolate alkali salts are widely used in organic synthesis, mainly due to their solubility in common organic solvents. They are frequently used as nucleophiles in ester hydrolysis, both in solution and solid-phase chemistry. However, they have also been used as mild bases or as specific reagents in some chemical transformations. Reactions employing trimethylsilanolate alkali salts as the key component are typically performed under mild reaction conditions. This review summarizes the utilization of trimethylsilanolate alkali salts in various organic transformations.1 Introduction2 Properties of Alkali Metal Trimethylsilanolates (TMSO[M])3 Trimethylsilanolate Alkali Salts in Organic Synthesis4 Conclusion


2017 ◽  
Vol 846 (2) ◽  
pp. 124 ◽  
Author(s):  
Ninette Abou Mrad ◽  
Fabrice Duvernay ◽  
Robin Isnard ◽  
Thierry Chiavassa ◽  
Grégoire Danger

RSC Advances ◽  
2016 ◽  
Vol 6 (28) ◽  
pp. 23242-23251 ◽  
Author(s):  
Lucie Brulikova ◽  
Soňa Krupkova ◽  
Maitia Labora ◽  
Kamil Motyka ◽  
Ludmila Hradilova ◽  
...  

Several Rhodamine B derivatives based on a tri-substituted pyrimidine core were prepared using solid-phase chemistry. Some derivatives exhibited fluorescence also at high pH and showed significant mitochondrial localization.


2015 ◽  
Vol 75-76 ◽  
pp. 309-314
Author(s):  
M.E. Palumbo ◽  
R.G. Urso ◽  
Z. Kaňuchová ◽  
C. Scirè ◽  
M. Accolla ◽  
...  

RNA ◽  
2012 ◽  
Vol 18 (4) ◽  
pp. 856-868 ◽  
Author(s):  
Y. Thillier ◽  
E. Decroly ◽  
F. Morvan ◽  
B. Canard ◽  
J.-J. Vasseur ◽  
...  

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