ChemInform Abstract: Ruthenium-Catalyzed Oxidation of Alkynes to 1,2-Diketones under Room Temperature and One-Pot Synthesis of Quinoxalines.

ChemInform ◽  
2013 ◽  
Vol 44 (23) ◽  
pp. no-no
Author(s):  
Yuan Xu ◽  
Xiaobing Wan
RSC Advances ◽  
2020 ◽  
Vol 10 (13) ◽  
pp. 7691-7697 ◽  
Author(s):  
Castelo B. Vilanculo ◽  
Márcio J. Da Silva ◽  
Milena Galdino Teixeira ◽  
Jesus Avendano Villarreal

In this work, the catalyst Na7PW11O39 was used in a new one-pot synthesis route to oxidize linalool to valuable derivatives (i.e., vinyltetrahydrofuran, vinyltetrahydropyran, and diepoxide), using a green oxidant (H2O2) at room temperature.


2012 ◽  
Vol 9 (4) ◽  
pp. 2239-2244 ◽  
Author(s):  
Hossein Anaraki-Ardakani ◽  
Maziar Noei ◽  
Mina Karbalaei-Harofteh ◽  
Shahab Zomorodbakhsh

A new and efficient one-pot synthesis of polysubstituted pyrrole derivatives by three-component reaction between dialkyl acetylenedicarboxylates, triphenylphosphine, 2-aminopyridin derivatives in the presence of arylglyoxals is described. The reactions were performed in dichloromethane at room temperature and neutral conditions and afforded high yields of products.


RSC Advances ◽  
2015 ◽  
Vol 5 (13) ◽  
pp. 10065-10071 ◽  
Author(s):  
Archana M. Das ◽  
Raju Khan ◽  
Manash P. Hazarika ◽  
Debjani Baruah ◽  
Purnajyoti D. Bhuyan

This paper presents a new method for fabricating biodegradable bio-polymeric nanoparticles via a convenient one-pot strategy at room temperature under stirring conditions for application to communicable diseases.


2018 ◽  
Vol 3 (5) ◽  
pp. 1512-1516 ◽  
Author(s):  
Jutika Devi ◽  
Subarna Jyoti Kalita ◽  
Dibakar Chandra Deka

Synthesis ◽  
2019 ◽  
Vol 51 (22) ◽  
pp. 4215-4230 ◽  
Author(s):  
Adesh Kumar Singh ◽  
Rapelly Venkatesh ◽  
Jeyakumar Kandasamy

The palladium-catalyzed one-pot synthesis of 2,3-deoxy-3-keto aryl C-glycosides is achieved from glycals and anilines in the presence of tert-butyl nitrite and aqueous HBF4 under mild conditions. This one-pot method stereospecifically provides α- and β-aryl glycosides (≥19:1 by NMR) in good yields at room temperature. The configuration at the C-3 position in the glycal determines the anomeric selectivity (i.e., α or β) of the desired products.


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