Head-to-tail cyclization for synthesis of naturally occurring cyclic peptides on organophosphous small-molecular supports

Author(s):  
Haidi Li ◽  
Junyou Li ◽  
Jie Chao ◽  
Zixin Zhang ◽  
Chuanguang Qin

To achieve the head-to-tail cyclic peptides via the liquid-phase on-support cyclization and synergistic self-cleavage strategy, 4,4’-bis(diphenylphosphinyloxyl) diphenyl ketoxime (BDKO) and 4-diphenyl phospholoxy benzyl alcohol (DPBA) were designed and prepared as...

Planta Medica ◽  
2011 ◽  
Vol 77 (12) ◽  
Author(s):  
D Craik ◽  
A Poth ◽  
M Colgrave ◽  
M Akcan ◽  
B Oku ◽  
...  

Author(s):  
Gui Chen ◽  
Kuiyi You ◽  
Xiangbo Gong ◽  
Fangfang Zhao ◽  
Zhenpan Chen ◽  
...  

An efficient method for highly selective preparation of the high value-added benzyl alcohol (BOL) and benzaldehyde (BAL) from liquid-phase catalytic oxidation of toluene with molecular oxygen over CeO2-MnOx composite oxides...


2015 ◽  
Vol 6 (8) ◽  
pp. 4889-4896 ◽  
Author(s):  
Florian Rohrbacher ◽  
Gildas Deniau ◽  
Anatol Luther ◽  
Jeffrey W. Bode

The α-ketoacid–hydroxylamine (KAHA) ligation enables the direct cyclization of unprotected peptides upon cleavage, without coupling reagents or purification of precursors. We report the synthesis of a library of 24 cyclic peptides and a detailed mechanistic study.


Author(s):  
Ke Xue ◽  
Shuyi Lv ◽  
Chunlei Zhu

Naturally-occurring saturated fatty acids (NSFAs) have emerged as a class of promising biomaterials due to their low cost, chemical stability, well-defined melting points, large heat of fusion, reversible solid-liquid phase...


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