Visible Light Mediated, Catalyst Free, One-Pot Convenient Synthesis of Dihydropyridines

2021 ◽  
Vol 18 ◽  
Author(s):  
Jia-Qi Di ◽  
Meng-Nan Chen ◽  
Ai-Dong Zhao ◽  
Zhan-Hui Zhang

: A simple, efficient and green protocol has been developed for the synthesis of polysubstituted dihydropyridines via one-pot, four-component reaction of aldehydes, arylamines, dialkyl acetylenedicarboxylate, and malononitrile. The reaction was proceeded at room temperature in the absence of catalyst in aqueous ethyl lactate under visible light irradiation. The main advantages of the present approach are mild reaction condition, high yield, no column chromatography, clean reaction profile, environmentally friendly and sustainable from the economic point of view

2016 ◽  
Vol 5 (4) ◽  
Author(s):  
Ramadan Ahmed Mekheimer ◽  
Abdullah Mohamed Asiri ◽  
Afaf Mohamed Abdel Hameed ◽  
Reham R. Awed ◽  
Kamal Usef Sadek

AbstractStarting from readily available 2-naphthol, aldehydes, aryl and alkylamines, a variety of Betti bases were efficiently synthesized utilizing a catalytic amount of cerium (IV) ammonium nitrate (CAN) at room temperature. This protocol has advantages of high yield, mild reaction conditions, no environmental pollution, diversity of reactants and simple work up procedure.


2019 ◽  
Vol 72 (12) ◽  
pp. 978 ◽  
Author(s):  
Dafne Saporito ◽  
Sergio A. Rodriguez ◽  
Maria T. Baumgartner

An eco-friendly and direct arylation of hydroxyaryls in water using photoinduced reactions with different substrates (1-bromo-2-naphthol, 1-iodo-2-naphthol, N-(2-iodophenyl)acetamide, 5-bromouracil, 2-iodo-N-methylbenzamide, and 2-iodobenzamide) was studied. For example, π-expanded coumarins, compounds with potential optical applications, were synthesized in very high yield, without the use of toxic reagents, in a one-pot reaction. In addition, we demonstrate that the irradiation source (halogen lamp) can be efficiently replaced by an LED without altering the reaction yield.


Synthesis ◽  
2018 ◽  
Vol 51 (02) ◽  
pp. 522-529 ◽  
Author(s):  
Deqing Shi ◽  
Lingna Wang ◽  
Tiancong Ma ◽  
Mingming Qiao ◽  
Qiangxian Wu ◽  
...  

A visible-light photoredox-catalyzed oxidation/[3+2] cycloaddition/oxidative aromatization cascade reaction of [(3,4-dihydroisoquinolin-2(1H)-yl)methyl]phosphonates and activated olefins or alkynes for the efficient synthesis of potentially biological active pyrrolo[2,1-a]isoquinoline-substituted phosphonates was developed. This transformation features mild reaction conditions (i.e., visible light irradiation, room temperature), molecular oxygen (O2) as a green oxidant, simple ‘one-pot’ operation.


RSC Advances ◽  
2016 ◽  
Vol 6 (59) ◽  
pp. 54236-54240 ◽  
Author(s):  
Seyed Mohsen Sadeghzadeh

A green and efficient method for the synthesis of various triazolo[1,2-a]indazoletrione under mild conditions is reported, that making it a genuinely green protocol.


2021 ◽  
Vol 8 ◽  
Author(s):  
Fa-Jie Chen ◽  
Zhenguo Hua ◽  
Jianhui Chen ◽  
Jiajia Chen ◽  
Daesung Lee ◽  
...  

Herein, we report an efficient method for the synthesis of (Z)-β-halovinyl ketones through a one-pot Sonogashira coupling and hydrohalogenation reaction promoted by palladium-copper catalyst and Brønsted acid. The ynone intermediates are generated in situ from readily available acid chlorides and terminal alkynes at room temperature, which are directly converted to (Z)-β-halovinyl ketones by treating with triflic acid. This method avoids the use of an external halogen source and features broad substrate scope, high yield, and good to excellent stereoselectivity.


1970 ◽  
Vol 4 (1) ◽  
pp. 137-141
Author(s):  
MA Aziz ◽  
MAM Miah ◽  
SM Sayem

The experiment was conducted at Bangladesh Rice Research Institute farm, Gazipur during the T. aman season, 2003 in order to determine the performance of Sunray organic fertilizer on the growth and yield of rice. The following eight treatment combinations were tested in wetland condition: T1= Native nutrient; T2 = Sunray Formula + G (SF) @ 100 kg/ha + Sunray Padiplus (PP) 20 ml @ 10 ml/4.5 lit./100m2 + Sunray Pady Segar (PS) @ 150 kg/ha + ( STB - N, P, K, S & Zn content in SF, PP & PS); T3= STB for high yield goal (HYG); T4= STB + 20 ml PP; T5= STB + 10 ml PP; T6= SF @ 400 kg/ha + ( STB - N, P, K, S & Zn content in 400 kg SF); T7= PS @ 400 kg/ha + (STB - N, P, K, S & Zn content in 400 kg PS ); T8= SF @ 200 kg/ha + PS@ 200 kg/ha + 10 ml PP + ( STB - N, P, K, S & Zn content in SF, PS and PP). The blanket doses of fertilizers were applied on soil test based (STB). BRRI dhan31 was used as test crop. The sources of N, P, K, S & Zn were Urea, TSP, MP, gypsum and zinc sulphate. Urea was applied into three equal splits, 1/3rd basal, 1/3rd maximum tillering stage and the remaining 1/3rd at panicle initiation stage. The treatment T2 where Sunray fertilizer were applied in combination with chemical fertilizer on STB produced substantially higher yield than those of other tested treatments. In terms of economic point of view this treatment also be considered as the most viable treatment in the experiment. Key words: Sunray, organic fertilizer, growth and yield, wetland rice.


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Fang-Fang Tan ◽  
Xiao-Ya He ◽  
Wan-Fa Tian ◽  
Yang Li

AbstractCleavage of C–O bonds in lignin can afford the renewable aryl sources for fine chemicals. However, the high bond energies of these C–O bonds, especially the 4-O-5-type diaryl ether C–O bonds (~314 kJ/mol) make the cleavage very challenging. Here, we report visible-light photoredox-catalyzed C–O bond cleavage of diaryl ethers by an acidolysis with an aryl carboxylic acid and a following one-pot hydrolysis. Two molecules of phenols are obtained from one molecule of diaryl ether at room temperature. The aryl carboxylic acid used for the acidolysis can be recovered. The key to success of the acidolysis is merging visible-light photoredox catalysis using an acridinium photocatalyst and Lewis acid catalysis using Cu(TMHD)2. Preliminary mechanistic studies indicate that the catalytic cycle occurs via a rare selective electrophilic attack of the generated aryl carboxylic radical on the electron-rich aryl ring of the diphenyl ether. This transformation is applied to a gram-scale reaction and the model of 4-O-5 lignin linkages.


2021 ◽  
Vol 19 ◽  
Author(s):  
Suman Swami ◽  
Rahul Shrivastava ◽  
Neelam Sharma ◽  
Arunava Agarwala ◽  
Ved Prakash Verma ◽  
...  

Abstract: 1,5-Disubstituted tetrazoles are vital drug-like scaffold usually encountered as valuable bioisosteres of cis-amide bond. In this article, we reported synthesis of some novel medicinally relevant pyrazole centered 1,5-disubstituted tetrazoles using ultrasound irradiation via a one-pot 4-C reaction from various pyrazole originated aldehyde, amine, isocyanide, and sodium azide. All the synthesized derivatives were characterized by IR, 1H NMR, 13C NMR, spectroscopic techniques, and mass analysis. This ultrasound-assisted green protocol has several advantages like mild reaction condition, high yield, catalyst and solvent-free reaction protocol, 15 minutes reaction time and easy workup.


2017 ◽  
Vol 41 (19) ◽  
pp. 11148-11154 ◽  
Author(s):  
Bhartendu Pati Tripathi ◽  
Anu Mishra ◽  
Pratibha Rai ◽  
Yogesh Kumar Pandey ◽  
Madhulika Srivastava ◽  
...  

Visible light mediated, an eco-friendlier synthetic protocol for dihydropyrano[2,3-c]pyrazoles via catalyst-free and solvent-free conditions at room temperature.


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