Ionic liquid-mediated biocatalyzed organic transformations

Author(s):  
Bubun Banerjee ◽  
Aditi Sharma
ChemInform ◽  
2015 ◽  
Vol 46 (32) ◽  
pp. no-no
Author(s):  
Pedavenkatagari Narayana Reddy ◽  
Pannala Padmaja ◽  
Basireddy V. Subba Reddy ◽  
Gundla Rambabu

RSC Advances ◽  
2016 ◽  
Vol 6 (24) ◽  
pp. 20306-20316 ◽  
Author(s):  
Somayyeh Sarvi Beigbaghlou ◽  
Katayoun Marjani ◽  
Azizollah Habibi ◽  
Seyyed Vahid Atghia

Ammonium hydrogen sulfate based ionic liquid immobilized on Na+–montmorillonite (AHS@MMT) was prepared via anchoring ammonium hydrogen sulfate propyltriethoxysilane onto sodium montmorillonite by covalent bonds.


2019 ◽  
Vol 6 (2) ◽  
pp. 177-182 ◽  
Author(s):  
Arijit Saha ◽  
Soumen Payra ◽  
Archana Asatkar ◽  
Ashok Raj Patel ◽  
Subhash Banerjee

Background: Recently, organic synthesis using ionic liquids (ILs) via green approach has attracted considerable attention to address the problem associated with environmental pollution. Magnetization of ILs provides added advantages of separation by external magnet. This can be accomplished by incorporation of high-spin iron(III) in the form of tetrachloro or tetrabromoferrate( III). Thus, synthesis of novel magnetically separable ILs for organic transformations is highly desirable. Results: [AcMIm]FeCl4 ionic liquid showed excellent catalytic activity in the one pot threecomponent synthesis tetrahydrobenzo[b]pyran derivatives at room temperature in excellent yields (94-98 %) within short reaction time (15-20 min.). The ILs were recovered and reused for at least six times with the minimum loss of catalytic activity. Methods: Here, we have demonstrated the excellent catalytic activity of acid functionalized magnetic Ils, [AcMIm]FeCl4 in one-pot multicomponent reactions for the synthesis of biologically important tetrahydrobenzo[b]pyran derivatives. Conclusion: A facile and convenient methodology has been developed for the synthesis of bio-active tetrahydrobenzo[b]pyran derivatives using [AcMIm]FeCl4 ionic liquid as an sufficient and reusable catalyst under environment-benign conditions.


2014 ◽  
Vol 2014 ◽  
pp. 1-13 ◽  
Author(s):  
Svetlana Ivanova

An overview of the recent advances in the field of polyoxometalate, ionic liquid hybrids, is proposed with a special attention paid to their application in catalysis, more precisely biphasic and heterogeneous catalysis. Both components of the hybrids are separately outlined pointing to their useful properties and potential for catalysis, followed by the description of the hybrids preparation and synergy between components in a large range of organic transformations. And finally a vision on the future developments is proposed.


Author(s):  
Shui-Ling Chen ◽  
Guan-Leong Chua ◽  
Shun-Jun Ji ◽  
Teck-Peng Loh

2018 ◽  
Vol 83 (10) ◽  
pp. 1071-1097 ◽  
Author(s):  
Gurpreet Kaur ◽  
Aditi Sharma ◽  
Bubun Banerjee

Heterocycles are the privileged structural subunit of many marketed drug molecules. On the other hand, the last decade has seen tremendous applications of the ionic liquid [bmim]PF6 (1-butyl-3-methyl-1H-imidazolium hexafluorophosphate) as an efficient, cheap, commercially available, low toxic reaction medium for various organic transformations. The present review summarizes recent reported applications of [bmim]PF6 as an efficient reaction medium for the synthesis of diverse biologically relevant heterocycles.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Sumit Ghosh ◽  
Debashis Ghosh ◽  
Alakananda Hajra

Abstract An environmentally benign, stable yet efficient organocatalyst is highly desirable from the viewpoint of green chemistry and catalysis. Imidazole-based zwitterionic-type molten salts are a new type of organocatalysts with high catalytic application in various organic transformations with added advantage of room temperature ionic liquid (RTIL) property. Most importantly, these ionic-liquid catalysts are easily recyclable and subsequently reusable for multiple times without loss of significant catalytic efficiency. It has also been evident that C2–H of the imidazole has a vital role in catalyzing the reaction via electrophilic activation. Moreover, by changing the cations and/or anions, the properties of ILs can be tuned in many ways. In this article, the role of imidazolium zwitterionic molten salts as an organocatalyst for selective organic transformations including syn-selective aza-Henry reaction, Erlenmeyer reaction, synthesis of different heterocycles and their functionalization and regioselective ring-opening reactions has been elaborated chronically which will definitely be helping to the readers to explore this new class of organocatalyst for further applications.


2018 ◽  
Vol 3 (19) ◽  
pp. 5283-5295 ◽  
Author(s):  
Gurpreet Kaur ◽  
Aditi Sharma ◽  
Bubun Banerjee

Sign in / Sign up

Export Citation Format

Share Document