Selective Oxidation of a Single Primary Alcohol Function in Oligopyridine Frameworks

2004 ◽  
Vol 6 (17) ◽  
pp. 2865-2868 ◽  
Author(s):  
Raymond Ziessel ◽  
Patrick Nguyen ◽  
Laurent Douce ◽  
Michèle Cesario ◽  
Claude Estournes
2011 ◽  
Vol 7 ◽  
pp. 1182-1188
Author(s):  
Abhishek Santra ◽  
Anup Kumar Misra

A convenient synthesis of the tetrasaccharide repeating unit of theO-antigen ofShigella boydiitype 9 has been achieved in excellent yield using a [2 + 2] block glycosylation strategy. TEMPO-mediated selective oxidation of the primary alcohol of the tetrasaccharide derivative8to the carboxylic group followed by deprotection of the functional groups furnished target tetrasaccharide1as its 4-methoxyphenyl glycoside in high yield.


2013 ◽  
Vol 22 (3) ◽  
pp. 621-629
Author(s):  
Seon Min Ahn ◽  
Kyung Min Park ◽  
Seung Jun Choi ◽  
Seokwon Lim ◽  
Dong-Hyun Kang ◽  
...  

2003 ◽  
Vol 78 (1-4) ◽  
pp. 281-290 ◽  
Author(s):  
Yuichi Kamiya ◽  
Satoshi Ueki ◽  
Norihito Hiyoshi ◽  
Naoki Yamamoto ◽  
Toshio Okuhara

Synthesis ◽  
1987 ◽  
Vol 1987 (11) ◽  
pp. 1012-1013 ◽  
Author(s):  
Rainer Mahrwald ◽  
Fritz Theil ◽  
Hans Schick ◽  
Hans-Joachim Palme ◽  
Heidrun Nowak ◽  
...  

2013 ◽  
Vol 800 ◽  
pp. 424-427
Author(s):  
Gong De Wu ◽  
Xiao Li Wang ◽  
Xian Feng Liu ◽  
Xiao Tian Zhang

A fluorine anion modified CuNiAl hydrotalcite (CuNiAl-LDH (F-)) was prepared for the selective oxidation of glycerol (GLY) using O2 as oxidant. It was found that the obtained catalyst with typical layer structures of hydrotalcite compounds was an effective heterogeneous catalyst in GLY oxidation. Under the present conditions, the main product was the C3 oxygenated products of primary alcohol glyceric acid (GLYAC). The highest conversion of GLY reached 32.0% with 58.1% of the selectivity to GLYAC.


2020 ◽  
Vol 44 (21) ◽  
pp. 8710-8717
Author(s):  
André L. D. Lima ◽  
Humberto V. Fajardo ◽  
André E. Nogueira ◽  
Márcio C. Pereira ◽  
Luiz C. A. Oliveira ◽  
...  

Nb-peroxo@iron oxides show high selectivity and activity in aniline conversion to azoxybenzene.


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