ChemInform Abstract: Benzenes Carrying Sulfonyl, Sulfinyl, or Sulfenyl Functional Groups, But Excluding Those Compounds Bearing Functionalized Side Chains

ChemInform ◽  
2010 ◽  
Vol 27 (51) ◽  
pp. no-no
Author(s):  
R. W. BROWN
2017 ◽  
Vol 5 (6) ◽  
pp. 2473-2477 ◽  
Author(s):  
Chandima Bulumulla ◽  
Jia Du ◽  
Katherine E. Washington ◽  
Ruvanthi N. Kularatne ◽  
Hien Q. Nguyen ◽  
...  

The incorporation of functional groups into the side chains of polythiophenes can improve the phase separation of polymer : nanoparticle hybrid solar cells (HSCs).


2010 ◽  
Vol 2010 ◽  
pp. 1-9 ◽  
Author(s):  
Keisuke Iida ◽  
Masayuki Tera ◽  
Takatsugu Hirokawa ◽  
Kazuo Shin-ya ◽  
Kazuo Nagasawa

Structure-activity relationship studies were carried out on macrocyclic hexaoxazole (6OTD) dimers, whose core structure stabilizes telomeric G-quadruplexes (G4). Two new 6OTD dimers having side chain amine and guanidine functional groups were synthesized and evaluated for their stabilizing ability against a telomeric G4 DNA sequence. The results show that the 6OTD dimers interact with the DNA to form 1:1 complexes and stabilize the antiparallel G4 structure of DNA in the presence of potassium cation. The guanidine functionalized dimer displays a potent stabilizing ability of the G4 structure, as determined by using a FRET melting assay (ΔTm=14 °C).


Author(s):  
luis camacho III ◽  
Bryan J. Lampkin ◽  
Brett VanVeller

We describe a method to protect the sensitive stereochemistry of the thioamide—in analogy to the protection of the functional groups of amino acid side chains—in order to preserve the thioamide moiety during peptide elongation.<br>


2000 ◽  
Vol 112 (24) ◽  
pp. 11069-11079 ◽  
Author(s):  
David G. Shirvanyanz ◽  
Alexander S. Pavlov ◽  
Pavel G. Khalatur ◽  
Alexei R. Khokhlov

2021 ◽  
Vol 54 (7) ◽  
pp. 3478-3488
Author(s):  
Seongwon Yoon ◽  
Keun Jun Lee ◽  
Sungmin Park ◽  
Taehee Kim ◽  
Sang Hyuk Im ◽  
...  

1965 ◽  
Vol 32 (2) ◽  
pp. 193-201 ◽  
Author(s):  
R. D. Hill ◽  
Raione R. Laing

Summaryk-Casein and whole casein when photo-oxidized in the presence of methylene blue lose the ability to clot when treated with rennin. Two effects are involved—first the photo-oxidation alters the k-casein fraction so that the rennin is unable to split off the glycopeptide fragment, and secondly, in whole casein the photo-oxidation interferes with the aggregation in the presence of Ca++that normally follows rennin action. As a result of amino acid analysis and specific treatments which affect other photo-oxidizable side chains, it is concluded that both of these effects are caused by the alteration of histidines.


2020 ◽  
Vol 11 (2) ◽  
pp. 508-516 ◽  
Author(s):  
Kuluni Perera ◽  
Zhengran Yi ◽  
Liyan You ◽  
Zhifan Ke ◽  
Jianguo Mei

This work illustrates an effective side-chain modification approach using amide functional groups to induce aqueous electroactivity to ProDOT-based electrochromic polymers.


Sign in / Sign up

Export Citation Format

Share Document