Carbon-Carbon and Carbon-Heteroatom Bond-forming Reactions under Greener Conditions-Part 1B

Author(s): Bubun Banerjee

Journal Name: Current Organic Chemistry

Volume 24 , Issue 1 , 2020


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[1]
Brahmachari, G.; Banerjee, B. Sulfamic acid-catalyzed carbon-carbon and carbon-heteroatom bond forming reactions: an overview. Curr. Organocatal., 2016, 3, 93-124.
[http://dx.doi.org/10.2174/2213337202666150812230830]
[2]
Banerjee, B. Recent developments on ultrasound assisted catalyst-free organic synthesis. Ultrason. Sonochem., 2017, 35, Pt A-1-14.
[http://dx.doi.org/10.1016/j.ultsonch.2016.09.023] [PMID: 27771266 ]
[3]
Brahmachari, G.; Banerjee, B. Catalyst-free organic synthesis at room temperature in aqueous and non-aqueous media: an emerging field of green chemistry practice and sustainability. Curr. Green Chem., 2015, 2, 274-305.
[http://dx.doi.org/10.2174/2213346102666150218195142]
[4]
Banerjee, B. Recent developments on ultrasound-assisted one-pot multicomponent synthesis of biologically relevant heterocycles. Ultrason. Sonochem., 2017, 35, Pt A-15-35.
[http://dx.doi.org/10.1016/j.ultsonch.2016.10.010] [PMID: 27771265 ]
[5]
Banerjee, B. Recent developments on organo-bycyclo-bases catalyzed multicomponent synthesis of biologically relevant heterocycles. Curr. Org. Chem., 2018, 22, 208-233.
[http://dx.doi.org/10.2174/1385272821666170703123129]
[6]
Banerjee, B.; Tajti, A.; Keglevich, G. Ultrasound-assisted synthesis of organophosphorus compounds. Organophosphorus chemistry: novel developments., Eds.; György Keglevich Berlin, Boston: De Gruyter. 2018, pp. 248-263.
[http://dx.doi.org/10.1515/9783110535839-013]
[7]
Banerjee, B. Ultrasound and nano-catalysts: an ideal and sustainable combination to carry out diverse organic transformations. ChemistrySelect, 2019, 4, 2484-2500.
[http://dx.doi.org/10.1002/slct.201803081]
[8]
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.
[http://dx.doi.org/10.1002/slct.201803600]
[9]
Kaur, G.; Sharma, A.; Banerjee, B. Ultrasound and ionic liquid: an ideal combination for organic transformations. ChemistrySelect, 2018, 3, 5283-5295.
[http://dx.doi.org/10.1002/slct.201800326]
[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.
[http://dx.doi.org/10.1002/slct.201802824]
[11]
Ujwaldev, S.M.; Rohit, K.R.; Radhika, S.; Anilkumar, G. Sonochemistry in transition metal catalyzed cross coupling reactions: recent developments. Curr. Org. Chem., 2019, 23, 3137-3153.
[http://dx.doi.org/10.2174/1385272823666191118103844]
[12]
Kerru, N.; Maddila, S.; Jonnalagadda, S.B. Design of carbon–carbon and carbon-heteroatom bond formation reactions under green conditions. Curr. Org. Chem., 2019, 23, 3154-3190.
[http://dx.doi.org/10.2174/1385272823666191202105820]
[13]
Banerjee, B.; Bhardwaj, V.; Kaur, A.; Kaur, G.; Arvind, S. Catalytic applications of saccharin and its derivatives in organic synthesis. Curr. Org. Chem., 2019, 23, 3191-3205.
[http://dx.doi.org/10.2174/1385272823666191121144758]
[14]
Sonawane, A.D.; Koketsu, M. Recent advances on C-Se bond forming reactions at low and room temperature. Curr. Org. Chem., 2019, 23, 3206-3225.
[http://dx.doi.org/10.2174/1385272823666191209111934]
[15]
Abd-Elmonem, M.; Mekheimer, R.A.; Hayallah, A.M.; Elsoud, F.A.A. Sadek, K.U. Recent Advances in the utility of glycerol as a benign and biodegradable medium in heterocyclic synthesis. Curr. Org. Chem., 2019, 23, 3226-3246.
[http://dx.doi.org/10.2174/1385272823666191025150646]
[16]
Molnar, M.; Lončarić, M.; Kovač, M. Green chemistry approaches to the synthesis of coumarin derivatives. Curr. Org. Chem., 2020, 24(1), 4-43.
[http://dx.doi.org/10.2174/1385272824666200120144305]
[17]
Mondal, A.; Mukhopadhyay, C. Construction of carbon-carbon and carbon-heteroatom bonds: Enabled by visible light. Curr. Org. Chem., 2020, 24(1), 44-73.
[18]
Li, X.; Liu, T.; Zhang, B.; Zhang, D.; Shi, H.; Yu, Z.; Tao, S.; Du, Y. Formation of carbon-carbon bonds mediated by hypervalent iodine reagents under metal-free conditions. Curr. Org. Chem., 2020, 24(1), 74-103.


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Article Details

VOLUME: 24
ISSUE: 1
Year: 2020
Page: [2 - 3]
Pages: 2
DOI: 10.2174/138527282401200305142223

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