Efficient Green Chemistry Approach for the Synthesis of 1,2,3-Triazoles Using Click Chemistry through Cycloaddition Reaction: Synthesis and Cytotoxic Study

2021 ◽  
pp. 1-13
Author(s):  
Bhumit L. Gondaliya ◽  
Khushal M. Kapadiya
Keyword(s):  
Green Chemistry ◽  
Click Chemistry ◽  
Cycloaddition Reaction ◽  
Reaction Synthesis

When CuAAC 'Click Chemistry' goes heterogeneous

2016 ◽  
Vol 6 (4) ◽  
pp. 923-957 ◽  
Author(s):  
S. Chassaing ◽  
V. Bénéteau ◽  
P. Pale
Keyword(s):  
Heterogeneous Catalysis ◽  
Green Chemistry ◽  
Click Chemistry ◽  
Organic Synthesis ◽  
Copper Ions ◽  
Cycloaddition Reaction ◽  
Catch Up

Within the green chemistry context, heterogeneous catalysis is more and more applied to organic synthesis. The well known ‘click chemistry’ and especially its flagship, the copper-catalyzed azide–alkyne cycloaddition reaction (CuAAC), is now catch up by such heterogenisation process and copper ions or metals have been grafted or deposited on or into various solids, such as (bio)polymers, charcoal, silica, zeolites, POM or MOF.

scholarly journals Furoic Acid and Derivatives as Atypical Dienes in Diels-Alder Reactions

2021 ◽  
Author(s):  
Razvan Cioc ◽  
Tom Smak ◽  
Marc Crockatt ◽  
Jan Kees Van der Waal ◽  
Pieter C A Bruijnincx
Keyword(s):  
Green Chemistry ◽  
Cycloaddition Reaction ◽  
Building Blocks ◽  
Diels Alder ◽  
Furoic Acid

The furan Diels-Alder (DA) cycloaddition reaction has become an important tool in green chemistry, being central to the sustainable synthesis of many chemical building blocks. The restriction to electron-rich furans...

In situ 1,3-dipolar azide cycloaddition reaction: synthesis of functionalized d-glucose based chiral piperidine and oxazepine analogues

Tetrahedron ◽  
2004 ◽  
Vol 60 (23) ◽  
pp. 4959-4965 ◽  
Author(s):  
Subhankar Tripathi ◽  
Kaushik Singha ◽  
Basudeb Achari ◽  
Sukhendu B Mandal
Keyword(s):  
Cycloaddition Reaction ◽  
Reaction Synthesis

scholarly journals Lewis acid- and/or Lewis base-catalyzed [3+2] cycloaddition reaction: synthesis of pyrazoles and pyrazolines

2008 ◽  
Vol 49 (48) ◽  
pp. 6768-6772 ◽  
Author(s):  
Palakodety Radha Krishna ◽  
Empati Raja Sekhar ◽  
Florence Mongin
Keyword(s):  
Lewis Acid ◽  
Cycloaddition Reaction ◽  
Lewis Base ◽  
Reaction Synthesis

Advances in click chemistry for silica-based material construction

RSC Advances ◽  
2016 ◽  
Vol 6 (26) ◽  
pp. 21979-22006 ◽  
Author(s):  
Ghodsi Mohammadi Ziarani ◽  
Zahra Hassanzadeh ◽  
Parisa Gholamzadeh ◽  
Shima Asadi ◽  
Alireza Badiei
Keyword(s):  
Click Chemistry ◽  
Organic Synthesis ◽  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition

Click chemistry is undoubtedly the most powerful 1,3-dipolar cycloaddition reaction in organic synthesis.

Corrigendum to “In situ 1,3-dipolar azide cycloaddition reaction: synthesis of functionalized d-glucose based chiral piperidine and oxazepine analogues”

Tetrahedron ◽  
2005 ◽  
Vol 61 (25) ◽  
pp. 6154
Author(s):  
Subhankar Tripathi ◽  
Kaushik Singha ◽  
Basudeb Achari ◽  
Sukhendu B. Mandal
Keyword(s):  
Cycloaddition Reaction ◽  
Reaction Synthesis

Visible-Light-Promoted Three-Component Cycloaddition Reaction: Synthesis of 4-Functionalized 1,5-Disubstituted 1,2,3-Triazoles

2021 ◽  
Author(s):  
atul kumar ◽  
Navaneet Kumar ◽  
Deepak Bhadoria
Keyword(s):  
Visible Light ◽  
Cycloaddition Reaction ◽  
Reaction Synthesis ◽  
Terminal Alkynes ◽  
Sodium Salts ◽  
Three Component Reaction

A first visible-light promoted and photocatalyst-free three-component reaction protocol has been developed to synthesize 4-functionalized 1,5-disubstituted 1,2,3-triazoles from terminal alkynes, arylazides, and arylsulfinic acid sodium salts or arylsulfonyl hydrazides in...

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