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Current Organocatalysis

Editor-in-Chief

ISSN (Print): 2213-3372
ISSN (Online): 2213-3380

Editorial

Organocatalyst: A Valuable Tool for the Carbon-carbon and Carbonheteroatom bond Formations

Author(s): Bubun Banerjee

Volume 8, Issue 1, 2021

Published on: 29 January, 2021

Page: [3 - 4] Pages: 2

DOI: 10.2174/221333720801210129105038

[1]
Sultan, S.; Shah, B.A. Carbon‐carbon and carbon‐heteroatom bond formation reactions using unsaturated carbon compounds. Chem. Rec., 2019, 19, 644-660.
[2]
Brahmachari, G.; Banerjee, B. Sulfamic acid-catalyzed carbon-carbon and carbon-heteroatom bond forming reactions: An overview. Curr. Organocatal., 2016, 3, 93-124.
[3]
Banerjee, B. Recent developments on nano-ZnO catalyzed synthesis of bioactive heterocycles. J. Nanostructure Chem, 2017, 7, 389-413.
[4]
Banerjee, B. Sc(OTf)3 catalyzed carbon-carbon and carbon-heteroatom bond forming reactions: A review. ARKIVOC, 2017, i, 1-25.
[5]
Banerjee, B. Ultrasound and nano-catalysts: an ideal and sustainable combination to carry out diverse organic transformations. ChemistrySelect, 2019, 4, 2484-2500.
[6]
Kaur, G.; Devi, P.; Thakur, S.; Kumar, A.; Chandel, R.; Banerjee, B. Magnetically separable transition metal ferrites: versatile heterogeneous nano-catalysts for the synthesis of diverse bioactive heterocycles. ChemistrySelect, 2019, 4, 2181-2199.
[7]
Banik, B.; Banerjee, B.; Kaur, G.; Saroch, S.; Kumar, R. Tetrabutylammonium bromide (TBAB) catalyzed synthesis of bioactive heterocycles. Molecules, 2020, 25, 5918.
[http://dx.doi.org/10.3390/molecules25245918]
[8]
Banerjee, B. Recent developments on organo-bycyclo-bases catalyzed multicomponent synthesis of biologically relevant heterocycles. Curr. Org. Chem., 2018, 22, 208-233.
[9]
Kaur, G.; Bala, K.; Devi, S.; Banerjee, B. Camphorsulfonic acid (CSA): An efficient organocatalyst for the synthesis or derivatization of heterocycles with biologically promising activities. Curr. Green Chem., 2018, 5, 150-167.
[10]
Kaur, G.; Thakur, S.; Kaundal, P.; Chandel, K.; Banerjee, B. p-Dodecylbenzenesulfonic acid: An efficient brønsted acid-surfactant-combined catalyst to carry out diverse organic transformations in aqueous medium. ChemistrySelect, 2018, 3, 12918-12936.
[11]
Banerjee, B.; Bhardwaj, V.; Kaur, A.; Kaur, G.; Singh, A. Catalytic applications of saccharin and its derivatives in organic synthesis. Curr. Org. Chem., 2019, 23, 3191-3205.
[12]
Brahmachari, G.; Banerjee, B. Facile and one-pot access of 3,3-bis(indol-3-yl)indolin-2-ones and 2,2-bis(indol-3-yl)acenaphthylen-1(2H)-one derivatives via an eco-friendly pseudo-multicomponent reaction at room temperature using sulfamic acid as an organo-catalyst. ACS Sustainable Chem. Eng., 2014, 2, 2802-2812.
[13]
Brahmachari, G.; Banerjee, B. Facile and one-pot access to diverse and densely functionalized 2-amino-3-cyano-4H-pyrans and pyran-annulated heterocyclic scaffolds via an eco-friendly multicomponent reaction at room temperature using urea as a novel organo-catalyst. ACS Sustainable Chem. Eng., 2014, 2, 411-422.
[14]
Banerjee, B.; Brahmachari, G. Room temperature metal-free synthesis of aryl/heteroaryl-substituted bis(6-aminouracil-5-yl)methanes using sulfamic acid (NH2SO3H) as an efficient and eco-friendly organo-catalyst. Curr. Organocatal., 2016, 3, 125-132.
[15]
MacMillan, D.W.C. The advent and development of organocatalysis. Nature, 2008, 455, 304-308.
[16]
Kamanna, K. Amino acids and peptides organocatalysts: A brief overview on its evolution and applications in organic asymmetric synthesis. Curr. Organocatal., 2021, 8, 126-146.
[17]
Mondal, A.; Bhowmick, K.C. Asymmetric organocatalyzed warfarin synthesis in aqueous and nonaqueous media: A discussion in the era of COVID-19 pandemic. Curr. Organocatal., 2021, 8, 109-125.
[18]
Banerjee, B. Bismuth(III) triflate: An efficient catalyst for the synthesis of diverse biologically relevant heterocycles. ChemistrySelect, 2017, 2, 6744-6757.
[19]
Banerjee, B. [Bmim]BF4: A versatile ionic liquid for the synthesis of diverse bioactive heterocycles. ChemistrySelect, 2017, 2, 8362-8376.
[20]
Kaur, G.; Devi, M.; Kumari, A.; Devi, R.; Banerjee, B. One-pot pseudo five component synthesis of biologically relevant 1,2,6-triaryl-4-arylamino-piperidine-3-ene-3-carboxylates: A decade update. ChemistrySelect, 2018, 3, 9892-9910.
[21]
Banerjee, B. Recent developments on ultrasound-assisted synthesis of bioactive N-heterocycles at ambient temperature. Aust. J. Chem., 2017, 70, 872-888.
[22]
Banerjee, B. Recent developments on ultrasound-assisted one-pot multicomponent synthesis of biologically relevant heterocycles. Ultrason. Sonochem., 2017, 35, 15-35.
[23]
Kaur, G.; Sharma, A.; Banerjee, B. [Bmim]PF6: An efficient tool for the synthesis of diverse bioactive heterocycles. J. Serb. Chem. Soc., 2018, 83, 1071-1097.
[24]
Banerjee, B.; Kaur, G. Microwave-assisted catalyst-free synthesis of bioactive heterocycles. Curr. Microwave Chem., 2020, 7, 5-22.
[25]
Sarkar, R.; Mukhopadhyay, C. Organocatalytic synthesis of heterocycles: A brief overview covering recent aspects. Curr. Organocatal., 2021, 8, 93-108.
[26]
Demirbas, N.; Demirbas, A. Organocatalyzed heterocyclic transformations in green media: A review. Curr. Organocatal., 2021, 8, 27-711.
[27]
Agarwal, S.; Lathwal, A.; Nath, M. Recent advances on cellulose sulfuric acid as sustainable and environmentally benign organocatalyst for organic transformations. Curr. Organocatal., 2021, 8, 72-92.
[28]
Banerjee, B.; Koketsu, M. Recent developments in the synthesis of biologically relevant selenium-containing scaffolds. Coord. Chem. Rev., 2017, 339, 104-127.
[29]
Sonawane, A.D.; Koketsu, M. Organocatalysed synthesis of selenium containing scaffolds. Curr. Organocatal., 2021, 8, 5-26.
[30]
Kaur, G.; Singh, A.; Bala, K.; Devi, M.; Kumari, A.; Devi, S.; Devi, R.; Gupta, V.K.; Banerjee, B. Naturally occurring organic acid-catalyzed facile diastereoselective synthesis of biologically active (E)-3-(arylimino)Indolin-2-one derivatives in water at room temperature. Curr. Org. Chem., 2019, 23, 1778-1788.
[31]
Singh, A.; Kaur, G.; Kaur, A.; Gupta, V.K.; Banerjee, B. A general method for the synthesis of 3,3-bis(indol-3-yl)indolin-2-ones, bis(indol-3-yl)(aryl)methanes and tris(indol-3-yl)methanes using naturally occurring mandelic acid as an efficient organo-catalyst in aqueous ethanol at room temperature. Curr. Green Chem., 2020, 7, 128-140.
[32]
Kaur, G.; Shamim, M.; Bhardwaj, V.; Gupta, V.K.; Banerjee, B. Mandelic acid catalyzed one-pot threecomponent synthesis of α-aminonitriles and α-aminophosphonates under solvent-free conditions at room temperature. Synth. Commun. 2020, 50, 1545-1560..
[33]
Kaur, G.; Kumar, R.; Saroch, S.; Gupta, V.K.; Banerjee, B. Mandelic acid: An efficient organo-catalyst for the synthesis of 3-substituted-3-hydroxyindolin- 2-ones and related derivatives in aqueous ethanol at room temperature. Curr. Organocatal., 2021, 8, 147-159.

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