Methyl-triflate-mediated dearylmethylation of N-(arylmethyl)carboxamides via the retro-Mannich reaction induced by electrophilic dearomatization/rearomatization in an aqueous medium at room temperature

2019 ◽  
Vol 21 (9) ◽  
pp. 2252-2256
Author(s):  
Hui Peng ◽  
Jinhui Ma ◽  
Wenkun Luo ◽  
Guangwen Zhang ◽  
Biaolin Yin

Dearylmethylation of N-(arylmethyl)carboxamides was achieved under metal-free conditions in an aqueous medium induced by electrophilic dearomatization/rearomatization.

2017 ◽  
Vol 19 (22) ◽  
pp. 5385-5389 ◽  
Author(s):  
Amrendra Kumar ◽  
Ramanand Ramanand ◽  
Narender Tadigoppula

An efficient and metal-free method has been developed for the synthesis of polysubstituted pyrrole derivatives with combination of sodium dodecyl sulphate (SDS) and Triton X-100 surfactants using water as a solvent at room temperature in 2–6 h and under microwave conditions (10 min) with good to excellent yields.


2019 ◽  
Vol 43 (42) ◽  
pp. 16441-16444 ◽  
Author(s):  
Zan Yang ◽  
Liping Hu ◽  
Ting Cao ◽  
Li An ◽  
Lijun Li ◽  
...  

Herein, an efficient, metal-free process for the α-C–H thiocyanation of enaminones was developed using PhI(OAc)2 as an oxidant at room temperature in an aqueous medium.


2016 ◽  
Vol 52 (75) ◽  
pp. 11231-11234 ◽  
Author(s):  
Tapas Das ◽  
Anirban Kayet ◽  
Ruchika Mishra ◽  
Vinod K. Singh

A metal free route to highly fluorescent 1,2-dihydropyrimido[1,6-α]indole derivatives has been developedviabase catalyzed aldol followed by the Mannich reaction of indole-2-carboxaldehyde with ethylN-arylideneglycinate at room temperature.


Author(s):  
Ruisheng Liu ◽  
Qishun Liu ◽  
Haoran Meng ◽  
Hongyu Ding ◽  
Jindong Hao ◽  
...  

A metal-free and visible-light-induced strategy has been established for the construction of α-ketoesters via aerobic oxidation of α-diazoesters with dioxygen in air at room temperature.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Cheng Li ◽  
Yu Hui Huang ◽  
Jian-Jun Wang ◽  
Bo Wang ◽  
Yong Jun Wu ◽  
...  

AbstractSolid-state refrigeration which is environmentally benign has attracted considerable attention. Mechanocaloric (mC) materials, in which the phase transitions can be induced by mechanical stresses, represent one of the most promising types of solid-state caloric materials. Herein, we have developed a thermodynamic phenomenological model and predicted extraordinarily large elastocaloric (eC) strengths for the (111)-oriented metal-free perovskite ferroelectric [MDABCO](NH4)I3 thin-films. The predicted room temperature isothermal eC ΔSeC/Δσ (eC entropy change under unit stress change) and adiabatic eC ΔTeC/Δσ (eC temperature change under unit stress change) for [MDABCO](NH4)I3 are −60.0 J K−1 kg−1 GPa−1 and 17.9 K GPa−1, respectively, which are 20 times higher than the traditional ferroelectric oxides such as BaTiO3 thin films. We have also demonstrated that the eC performance can be improved by reducing the Young’s modulus or enhancing the thermal expansion coefficient (which could be realized through chemical doping, etc.). We expect these discoveries to spur further interest in the potential applications of metal-free organic ferroelectrics materials towards next-generation eC refrigeration devices.


Author(s):  
Yu-Fen Lv ◽  
Jinyun Luo ◽  
Yuchuan Ma ◽  
Qi Dong ◽  
Lin He

A new visible-light-mediated protocol has been proposed for the synthesis of thiosulfonates via metal-free sulfonylation of thiols with aryldiazonium and sodium metabisulphite at room temperature. This mild three-component reaction, simply...


RSC Advances ◽  
2016 ◽  
Vol 6 (27) ◽  
pp. 22320-22330 ◽  
Author(s):  
Nazia Kausar ◽  
Indranil Roy ◽  
Dipankar Chattopadhyay ◽  
Asish R. Das

Graphene oxide nanosheet catalyzed strategies for construction of 2,3-dihydroquinazolinones and quinazolin-4(3H)-ones starting from anthranilamide and an aldehyde/ketone in aqueous medium at room temperature have been realized.


Synlett ◽  
2021 ◽  
Author(s):  
Yadong Sun ◽  
Ablimit Abdukader ◽  
Yuhan Lu ◽  
Chenjiang Liu

AbstractA highly efficient method for the synthesis of 1,2,3-thiadiazoles has been developed by utilizing readily available tosylhydrazones and ammonium thiocyanate with ecofriendly EtOH as the solvent at room temperature. The reaction shows a wide scope of substrates and good functional-group tolerance. This protocol can be scaled up to a gram level and can be applied to coupling reactions with 4-(4-bromophenyl)-1,2,3-thiadiazole as the substrate.


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