Metal-Free, Acid-Promoted Synthesis of Imidazole Derivatives via a Multicomponent Reaction

2013 ◽  
Vol 15 (24) ◽  
pp. 6116-6119 ◽  
Author(s):  
Chung-Yu Chen ◽  
Wan-Ping Hu ◽  
Pi-Cheng Yan ◽  
Gopal Chandru Senadi ◽  
Jeh-Jeng Wang
ChemInform ◽  
2014 ◽  
Vol 45 (22) ◽  
pp. no-no
Author(s):  
Chung-Yu Chen ◽  
Wan-Ping Hu ◽  
Pi-Cheng Yan ◽  
Gopal Chandru Senadi ◽  
Jeh-Jeng Wang

2020 ◽  
Vol 22 (21) ◽  
pp. 7506-7512
Author(s):  
Lixiang Zhu ◽  
Xiaoyu Ren ◽  
Juan Du ◽  
Jia-Hong Wu ◽  
Jian-Ping Tan ◽  
...  

A transition-metal-free multicomponent cascade reaction of α-halogenated ketones, ortho-aminophenols, and aldehydes using a dipeptide phosphonium salt catalyst was developed for the construction of various 2H-1,4-benzoxazines.


2019 ◽  
Vol 362 (3) ◽  
pp. 487-492 ◽  
Author(s):  
Guoqiang Lu ◽  
Nan Luo ◽  
Fangpeng Hu ◽  
Zihui Ban ◽  
Zhenzhen Zhan ◽  
...  

2018 ◽  
Vol 14 ◽  
pp. 2689-2697 ◽  
Author(s):  
Robby Vroemans ◽  
Yenthel Verhaegen ◽  
My Tran Thi Dieu ◽  
Wim Dehaen

A new metal-free one-pot three-component procedure towards fully substituted triazolochromenes has been developed, starting from commercially available materials. Salicylaldehydes and nitroalkenes were reacted under solvent-free conditions, followed by a 1,3-dipolar cycloaddition of the intermediate 3-nitro-2H-chromenes with organic azides in a one-pot two-step sequence. The triazolochromenes were formed with complete regioselectivity and new biologically relevant structures were synthesized via extension of the developed procedure and via postfunctionalization. The mechanochemical synthesis was carried out for several salicylaldehydes and gave a clear improvement in the yield of the corresponding triazolochromenes and consequently showed to be a viable alternative for solid salicylaldehydes.


2019 ◽  
Vol 6 (19) ◽  
pp. 3401-3407 ◽  
Author(s):  
Xuanhua Guo ◽  
Chengdong Lv ◽  
Qaiser Mahmood ◽  
Li Zhou ◽  
Guangqiang Xu ◽  
...  
Keyword(s):  

A metal-free, acid-free and chemoselective N-dealkylation-N-nitrosation or C-nitration of N-alkyl anilines has been developed.


2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Shivanand Merugu ◽  
Vijaya Kumar Ponnamaneni ◽  
Ravi Varala ◽  
Syed Farooq Adil ◽  
Mujeeb Khan ◽  
...  

A series of (E)-3-(2-((5-(benzylideneamino)-1,3,4-thiadiazol-2-yl)thio) acetyl)-2H-chromen-2-one and its derivatives (4a-h) have been obtained using a one-pot multicomponent reaction with good yields. The compounds have been synthesized from 3-(2-bromoacetyl)chromen-2-ones (1), 5-amino-1,3,4-thiadiazole-2-thiol (2), and substituted benzaldehydes (3) in anhydrous ethanol and conc. H2SO4. Subsequently, all the synthesized compounds have been screened for their antimicrobial activity and characterized by analytical and spectral data.


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