Selectivity and activity in catalytic hydrogenation of azido groups over Pd nanoparticles on aluminum oxy-hydroxide

2016 ◽  
Vol 40 (11) ◽  
pp. 9550-9555 ◽  
Author(s):  
Belgüzar Yasemin Kara ◽  
Benan Kılbaş ◽  
Haydar Göksu

A practical and effective catalytic method has been developed for the reduction of aryl azides in the presence of PdAlO(OH) nanoparticles and sodium borohydride.

1981 ◽  
Vol 46 (9) ◽  
pp. 2123-2128 ◽  
Author(s):  
Jiří Křepelka ◽  
Jiří Holubek

Lactones VI-IX were prepared on reduction of anhydrides of 4-aryl-1-methoxynaphthalene-2,3-dicarboxylic acids IV and V with sodium borohydride in methanol. Catalytic hydrogenation on platinum of lactones VIII and IX gave lactones with hydrogenated ring A, or A and C. Lactones XII and XIII were found to possess an inhibitory effect on the growth of the tumour S 37 in experimental animals.


RSC Advances ◽  
2014 ◽  
Vol 4 (104) ◽  
pp. 59977-59980 ◽  
Author(s):  
Xu Zhang ◽  
Zhiyu Wang ◽  
Shuang Li ◽  
Chunlei Wang ◽  
Jieshan Qiu

Highly compressible graphene aerogels were made by chemical reduction of graphene oxide with HI, which act as recyclable catalyst to exhibit excellent catalytic performance towards selective semi-hydrogenation reaction after loading Pd nanoparticles.


1977 ◽  
Vol 55 (6) ◽  
pp. 1100-1103 ◽  
Author(s):  
Hans H. Baer ◽  
Fawzy F. Z. Georges

The synthesis of 2,3,6-trideoxy-3-dimethylamino-D-arabino-hexose hydrochloride (10) (D-angolosamine, a constituent of the antibiotic, angolamycin) is described. First, a simplified procedure for the preparation of methyl 6-deoxy-α-D-glucopyranoside from methyl α-D-glucopyranoside is recorded. The deoxy derivative served as the starting point for sequential preparation of methyl 3,6-dideoxy-3-nitro-α-D-glucopyranoside (1), its 2,4-diacetate (2), its 4-monoacetate (3), its 2-O-mesyl-4-acetate (4), its 2-mesylate (5), and methyl 2,3,6-trideoxy-3-nitro-α-D-erythro-hex-2-enopyranoside (6) essentially according to procedures previously established (in part, in the L-series). Treatment of 5 or 6 with sodium borohydride produced methyl 2,3,6-trideoxy-3-nitro-α-D-arabino-hexopyranoside (7). Catalytic hydrogenation of 7 gave the corresponding 3-amino glycoside hydrochloride (8) which was hydrolyzed to furnish 3-amino-2,3,6-trideoxy-D-arabino-hexose hydrochloride (9) (D-acosamine, the enantiomer of a component of the antibiotic, actinoidin). N,N-Dimethylation of 8 followed by hydrolysis afforded the crystalline title compound (10).


Nanoscale ◽  
2015 ◽  
Vol 7 (42) ◽  
pp. 17786-17790 ◽  
Author(s):  
Jie S. Zhu ◽  
Young-Seok Shon

Unsupported thiolate-capped palladium nanoparticle catalysts are found to be highly substrate-selective for alkene hydrogenation and isomerization.


1968 ◽  
Vol 46 (17) ◽  
pp. 2793-2797 ◽  
Author(s):  
Hans H. Baer ◽  
Margaret C. T. Wang

Treatment of trans,trans-2-nitro-1,3-cyclohexanediol diacetate with ammonia followed by acetylation gives trans,trans 1,3-diacetamido-2-nitrocyclohexane (4). Catalytic hydrogenation of 4 and subsequent acetylation lead to trans,trans-2,6-diacetamidocyclohexylamine (5) and trans,trans-1,2,3-triacetamidocyclohexane (6), respectively. Permanganate oxidation of 4 affords cis-2,6-diacetamidocyclohexanone (7; 2,4-dinitrophenylhydrazone, 8). Sodium borohydride reduction of 7 produces trans,trans-2,6-diacetamidocyclohexanol (9; O-acetate, 10).


RSC Advances ◽  
2015 ◽  
Vol 5 (54) ◽  
pp. 43885-43896 ◽  
Author(s):  
Kun-Yi Andrew Lin ◽  
Shen-Yi Chen

Catalytic hydrogenation of bromate is a promising approach to remove bromate from water considering that this approach not only removes bromate but also converts it to bromide.


2020 ◽  
Vol 44 (9) ◽  
pp. 3681-3689 ◽  
Author(s):  
Yizhu Lei ◽  
Zaifei Chen ◽  
Guosong Lan ◽  
Renshu Wang ◽  
Xiao-Yu Zhou

Small palladium nanoparticles stabilized with phosphine-functionalized PIP displayed high catalytic activity for nitroarenes hydrogenation. Nano-size Pd particles, electron-donation effect of phosphine ligand, and surface wettability account for its excellent catalytic performance.


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