A mild and highly efficient one-pot three-component reaction for carbon–sulfur bond formation catalyzed by potassium tert-butoxide

Author(s):  
Barahman Movassagh ◽  
Amir Rakhshani
2019 ◽  
Vol 6 (1) ◽  
pp. 69-76
Author(s):  
Km N. Shivhare ◽  
Ibadur R. Siddiqui

Background: A green, recyclable and reusable chitosan catalyst has been utilized for the synthesis of 5-amino-2,3-dihydrobenzo[d]thiazole-4,6-dicarbonitrile and its derivatives. Methods and Results: Three-component reaction protocol incorporates the reaction of aldehydes, malononitrile and rhodanine derivatives. This is examined as an efficient route for the synthesis of dicarbonitriles utilizing a green, biodegradable, environmentally benign, and easily available chitosan catalyst. In the reported protocol, catalyst can be recycled and not any substantial dropping in its catalytic activity during the recycling steps was obtained. Conclusion: A green and environmentally benign, one pot three-component protocol has been illustrated for the synthesis of 5-amino-2,3-dihydrobenzo[d]thiazole-4,6-dicarbonitrile derivatives. Adequately yield products were gained via the natural catalytic approach with the recyclability of the catalyst. The use of chitosan represents this procedure as an attractive substitute for the synthesis of biaryls complex by multicomponent reaction condition.


Synthesis ◽  
2018 ◽  
Vol 50 (11) ◽  
pp. 2191-2199 ◽  
Author(s):  
Yongde Zhao ◽  
Shengqiang Guo ◽  
Yang Zhou ◽  
Bencai Dai ◽  
Cuimeng Huo ◽  
...  

A concise one-pot three-component reaction of organic halides­, terminal acetylenes, and sodium azide provided an efficient route for the synthesis of 1,2,3-triazoles. A variety of 1,2,3-triazoles were prepared in good to excellent yields with green solvent glycerol. This procedure used CuI and diethylamine, which are two easily available reagents as the new catalytic system at room temperature.


2016 ◽  
Vol 14 (1) ◽  
pp. 122-130 ◽  
Author(s):  
Deuk-Young Goo ◽  
Sang Kook Woo

We have developed a highly efficient synthetic route to carbazoles that employs sequential C–C/C–N bond formation via Suzuki cross-coupling and Cadogan cyclization. The developed method is compatible with electron neutral, rich or deficient substrates. The synthetic utility of this method was demonstrated by the concise syntheses of four natural products.


RSC Advances ◽  
2017 ◽  
Vol 7 (23) ◽  
pp. 13868-13875 ◽  
Author(s):  
Jie Mou ◽  
Gan Gao ◽  
Chen Chen ◽  
Jie Liu ◽  
Jian Gao ◽  
...  

An efficient synthesis of Betti basesviaa one-pot three-component reaction of 2-naphthol, substituted aldehydes and anilines in aqueous media is reported.


2020 ◽  
Vol 44 (20) ◽  
pp. 8614-8620 ◽  
Author(s):  
Song-Tao Xiao ◽  
Cui-Ting Ma ◽  
Jia-Qi Di ◽  
Zhan-Hui Zhang

An approach was developed for the synthesis of 2,4-disubstituted quinoline derivatives via a one pot three-component reaction of aromatic amines, aldehydes and alkynes catalyzed by MOF-5 under solvent-free conditions.


Author(s):  
Suman Das ◽  
Parveen Rawal ◽  
Jayeeta Bhattacharjee ◽  
Ajitrao Devadkar ◽  
Kuntal Pal ◽  
...  

An efficient catalytic process for the synthesis of α-aminophosphonates is developed by a one-pot three-component reaction in the presence of In complexes at room temperature. DFT based mechanistic studies of the catalytic reactions are reported.


Synthesis ◽  
2019 ◽  
Vol 51 (09) ◽  
pp. 2023-2029 ◽  
Author(s):  
Yue Zhu ◽  
Wenteng Chen ◽  
Donghong Zhao ◽  
Guolin Zhang ◽  
Yongping Yu

Polysubstituted 2-aminothiazoles have been synthesized via a one-pot three-component reaction of α-nitro epoxides, potassium thiocyanate, and primary amines without the need for any additives. This reaction proceeds smoothly in a highly efficient and eco-friendly manner with good to excellent yields. A possible mechanism is also proposed.


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