ChemInform Abstract: Zirconyl Chloride Promoted Highly Efficient Solid Phase Synthesis of Amide Derivatives.

ChemInform ◽  
2008 ◽  
Vol 39 (22) ◽  
Author(s):  
Cherkupally Sanjeeva Reddy ◽  
Adki Nagaraj ◽  
Pochampally Jalapathi
2007 ◽  
Vol 18 (10) ◽  
pp. 1213-1217 ◽  
Author(s):  
Cherkupally Sanjeeva Reddy ◽  
Adki Nagaraj ◽  
Pochampally Jalapathi

2015 ◽  
Vol 9 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Dongxin Zhao ◽  
Li Ma ◽  
Kui Lu ◽  
Juan He

Ferulic acid was used as a common drug for cardia-cerebrovascular disease and leukopenia, but the application of ferulic acid was inhibited by the poor absorption and stability. The improvement of these defects can be realized by modifying ferulic acid by amino acids, because the amido bond can increase the bioavailability and therapeutic effect of some drugs based on the peptide transporter system of mammalian which can transport the peptidyl drugs. The peptidyl derivatives of ferulic acid, namely acetyl feruloyl tyrosine and acetyl feruloyl valyl tyrosine, were synthesized using Fmoc solid-phase synthesis method. The synthesized ferulic acid amide derivatives were purified by RP-HPLC, and characterized by IR, HNMR and ESI-MS. The results indicated that Fmoc solid phase synthesis was a convenient method for the amide bond modification of ferulic acid and the further property research on ferulic acid derivatives.


2013 ◽  
Vol 9 ◽  
pp. 2395-2403 ◽  
Author(s):  
Felix Wojcik ◽  
Sinaida Lel ◽  
Alexander G O’Brien ◽  
Peter H Seeberger ◽  
Laura Hartmann

We present the solid phase synthesis of carbohydrate-functionalized oligo(amidoamines) with different functionalization patterns utilizing a novel alphabet of six differently glycosylated building blocks. Highly efficient in flow conjugation of thioglycosides to a double-bond presenting diethylentriamine precursor is the key step to prepare these building blocks suitable for fully automated solid-phase synthesis. Introduction of the sugar ligands via functionalized building blocks rather than postfunctionalization of the oligomeric backbone allows for the straightforward synthesis of multivalent glycoligands with full control over monomer sequence and functionalization pattern. We demonstrate the potential of this building-block approach by synthesizing oligomers with different numbers and spacing of carbohydrates and also show the feasibility of heteromultivalent glycosylation patterns by combining building blocks presenting different mono- and disaccharides.


2014 ◽  
Vol 12 (12) ◽  
pp. 1879-1884 ◽  
Author(s):  
Koushik Chandra ◽  
Tapta Kanchan Roy ◽  
Johnny N. Naoum ◽  
Chaim Gilon ◽  
R. Benny Gerber ◽  
...  

In situ peptide acetylation.


Sign in / Sign up

Export Citation Format

Share Document