Regioselective Synthesis of Functionalized 1,3‐Thiazine‐4‐ones via Multicomponent Click Reaction Approach

2019 ◽  
Vol 4 (2) ◽  
pp. 650-654 ◽  
Author(s):  
Abdulkadir Shube Hussen ◽  
Aparna Monga ◽  
Anuj Sharma
Keyword(s):  
Click Reaction ◽  
Regioselective Synthesis

Regioselective synthesis of multisubstituted 1,2,3-triazoles: moving beyond the copper-catalyzed azide–alkyne cycloaddition

2016 ◽  
Vol 52 (99) ◽  
pp. 14188-14199 ◽  
Author(s):  
Fang Wei ◽  
Weiguo Wang ◽  
Yudao Ma ◽  
Chen-Ho Tung ◽  
Zhenghu Xu
Keyword(s):  
Recent Progress ◽  
Click Reaction ◽  
Regioselective Synthesis ◽  
Efficient Synthesis ◽  
Feature Article

Copper(i)-catalyzed azide–alkyne cycloaddition (CuAAC) provides an efficient synthesis of 1,4-disubstituted 1,2,3-triazoles. This feature article highlights the recent progress on the regisoselective synthesis of multisubstituted 1,2,3-triazoles, which current click reaction (CuAAC) is unable to do.

Synthesis, structure, and catalytic activities of new Cu(i) thiocarboxylate complexes

RSC Advances ◽  
2014 ◽  
Vol 4 (75) ◽  
pp. 39790-39797 ◽  
Author(s):  
Deepak Kumar Joshi ◽  
Kunj Bihari Mishra ◽  
Vinod Kumar Tiwari ◽  
Subrato Bhattacharya
Keyword(s):  
Click Reaction ◽  
Regioselective Synthesis ◽  
Catalytic Activities

Newly synthesized Cu(i) with thiobenzoate complexes was found to catalyse the regioselective synthesis of glycoconjugate triazoles under click reaction.

ChemInform Abstract: Copper Immobilized on Nanosilica Triazine Dendrimer (Cu(II)-TD@nSiO2)-Catalyzed Regioselective Synthesis of 1,4-Disubstituted 1,2,3-Triazoles and Bis- and Tris-Triazoles via a One-Pot Multicomponent Click Reaction.

ChemInform ◽  
2014 ◽  
Vol 45 (30) ◽  
pp. no-no
Author(s):  
Mahboobeh Nasr-Esfahani ◽  
Iraj Mohammadpoor-Baltork ◽  
Ahmad R. Khosropour ◽  
Majid Moghadam ◽  
Valiollah Mirkhani ◽  
...  
Keyword(s):  
Click Reaction ◽  
Regioselective Synthesis ◽  
One Pot

scholarly journals Regioselective synthesis, characterization and antimicrobial evaluation of amide-ether linked 1,4-disubstituted 1,2,3-triazoles

2017 ◽  
Vol 82 (9) ◽  
pp. 995-1007 ◽  
Author(s):  
Chander Kaushik ◽  
Krishan Kumar ◽  
Devinder Kumar ◽  
Satbir Mor ◽  
Ashwani Kumar ◽  
...  
Keyword(s):  
Click Reaction ◽  
Docking Simulation ◽  
Regioselective Synthesis ◽  
Spectral Techniques ◽  
E Coli ◽  
Gram Positive Bacteria ◽  
Aspergillus Brasiliensis ◽  
Antimicrobial Evaluation ◽  
Ft Ir

Regioselective synthesis of some amide?ether-linked 1,4-disubstituted 1,2,3-triazoles was realized via the copper(I)-catalyzed click reaction of 1-(prop-2-ynyloxy)naphthalene, 2-(prop-2-ynyloxy)naphthalene and 1,4-bis-(prop-2-ynyloxy)benzene with 2-azido-N-substituted acetamides. The synthesized compounds were characterized by spectral techniques viz. FT-IR, 1H- -NMR, 13C-NMR, HRMS and evaluated for their in vitro antimicrobial activity against Bacillus subtilis, Staphylococcus aureus (Gram-positive bacteria), Pseudomonas aeruginosa, Escherichia coli (Gram-negative bacteria), Candida albicans and Aspergillus brasiliensis (fungi). Among the synthesized 1,4-disubstituted 1,2,3-triazoles, compound 13d displayed excellent antibacterial potential, while, compounds 7d and 13d appeared as potent fungicidal agents against the tested microbial strains. The docking simulation of the broad spectrum microbicidal disubstituted 1,2,3-triazole 13d into the active site of E. coli type II topoisomerase, DNA gyrase B enzyme was also investigated.

Bis-triazologlycolipid mimetics – low molecular weight organogelators

2014 ◽  
Vol 38 (7) ◽  
pp. 3015-3021 ◽  
Author(s):  
Arasappan Hemamalini ◽  
Thangamuthu Mohan Das
Keyword(s):  
Molecular Weight ◽  
Self Assembly ◽  
Click Reaction ◽  
Regioselective Synthesis ◽  
Low Molecular Weight ◽  
Low Molecular Weight Organogelators

A facile regioselective synthesis of bis-triazologlycolipids, a class of organogelators, has been accomplished by “Click reaction”. The morphology and self-assembly of the gelators were examined by FESEM and HRTEM analysis.

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