Synthesis and characterization of click-decahydrodecaborate derivatives by the copper(I) catalyzed [3+2] azide-alkyne cycloaddition reaction

2018 ◽  
Vol 865 ◽  
pp. 89-94 ◽  
Author(s):  
Suzan El Anwar ◽  
Zahra Laila ◽  
Ron Ramsubhag ◽  
Sami Tlais ◽  
Ali Safa ◽  
...  
2018 ◽  
Vol 42 (1) ◽  
pp. 272-280 ◽  
Author(s):  
Kan Zhang ◽  
Yuefeng Bai ◽  
Chun Feng ◽  
Guanghui Ning ◽  
Hailiang Ni ◽  
...  

A series of new H-shaped triphenylene discotic liquid crystal tetramers has been designed and synthesized using a copper-free [3+2] cycloaddition reaction.


2020 ◽  
Vol 17 ◽  
Author(s):  
Mukesh C. Joshi

: Novel group of phenoxy-substituted enediyne-triazole-conjugates were synthesized by Huisgen [3+2] cycloaddition reaction (Click chemistry) in aqueous media. The author found that enediynes were stable in aqueous medium and open air conditions.


2016 ◽  
Vol 13 (2) ◽  
pp. 298-306
Author(s):  
Baghdad Science Journal

This paper includes the synthesis of some new nucleoside analogues starting with 2-substituted benzimidazole derivative (7-9), that synthesized by condensation of O-phenylenediamine with p-chloro benzaldehyde and two substituted benzoic acid , which on nucleophilic substitution with propargyl bromide gave a new N-substituted compounds (10-12). D-Fructose and D-galactose were chosen as a sugar moiety which were protected, brominated and azotated to give azido sugars (5) and (6), then they were subjected to 1,3-dipolar cycloaddition reaction with N-substuted compounds afforded bloked nucleoside analoges (13-16), which after hydrolysis gave our target the free nucleoside analogues (17-20). All prepared compounds were identified by FT-IR and some of them with 1H-NMR and 13C-NMR.


2021 ◽  
Vol 2 (1) ◽  
pp. 1-7
Author(s):  
F. Serigne Abdou Khadir ◽  
S. Boukhssas ◽  
S. Achamlale ◽  
Y. Aouine ◽  
A. Nakkabi ◽  
...  

The biheterocyclic derivative of the phosphonic glycine analogue is prepared selectively by reaction between the α-azidoamino diethyl methylphosphonate and the 1-(prop-2-yn-1-yl)-1H-benzo[d]imidazole. The dipolar -1,3 cycloaddition reaction using Click Chemistry was carried out in a solvent water/ethanol mixture in a ratio of 1:1. Copper sulphate pentahydrate and sodium ascorbate are used in the reaction in catalytic amounts. The compound [diethyl [{4-[(1H-benzo[d]imidazol-1-yl)methyl]-1H-1,2,3-triazol-1-yl}(benzamido) methyl] phosphonate was isolated pure as a white powder, after chromatography on a silica gel column (ethyl acetate/hexane acetate: 1/1). The yield of pure product is 90%, after recrystallization in an ether/hexane mixture. The structure of the -1,4 isomer is attributed to the compound obtained by means of 1D and 2D NMR and based on data from the literature concerning the cycloaddition reaction via Click Chemistry. Two-dimensional NMR spectroscopy played a major role. The analysis of the different correlations between adjacent hydrogens and carbons, and also between hydrogens and distant carbons, confirmed the proposed structure.


1996 ◽  
Vol 61 (10) ◽  
pp. 3572-3572
Author(s):  
Lawrence T. Scott ◽  
Atena Necula

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