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Recent Developments on Five-Component Reactions

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2021 Apr 30
PMID 33915870
Citations 7
Authors
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Abstract

Multicomponent reactions (MCRs) have inherent advantages in pot, atom, and step economy (PASE). This important green synthetic approach has gained increasing attention due to high efficiency, minimal waste, saving resources, and straightforward procedures. Presented in this review article are the recent development on 5-compoment reactions (5CRs) of the following six types: (I) five different molecules A + B + C + D + E; pseudo-5CRs including (II) 2A + B + C + D, (III) 2A + 2B + C, (IV) 3A + B + C, (V) 3A + 2B, and (VI) 4A + B. 5CRs with more than five-reaction centers are also included.

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References
1.
Brauch S, van Berkel S, Westermann B . Higher-order multicomponent reactions: beyond four reactants. Chem Soc Rev. 2013; 42(12):4948-62. DOI: 10.1039/c3cs35505e. View

2.
Mobinikhaledi A, Bodaghifard M, Asadbegi S . A novel four- and pseudo-five-component reaction: unexpected efficient one-pot synthesis of 4H-thiopyran derivatives. Mol Divers. 2015; 20(2):461-8. DOI: 10.1007/s11030-015-9634-y. View

3.
Sengupta A, Maity S, Mondal A, Ghosh P, Rudra S, Mukhopadhyay C . Pseudo five component reaction towards densely functionalized spiro[indole-3,2'-pyrrole] by picric acid, an efficient syn-diastereoselective catalyst: insight into the diastereoselection on C(sp)-C(sp) axial conformation. Org Biomol Chem. 2019; 17(5):1254-1265. DOI: 10.1039/c8ob02849d. View

4.
Biswal P, Banjare S, Pati B, Mohanty S, Ravikumar P . Rhodium-Catalyzed One-Pot Access to N-Polycyclic Aromatic Hydrocarbons from Aryl Ketones through Triple C-H Bond Activations. J Org Chem. 2020; 86(1):1108-1117. DOI: 10.1021/acs.joc.0c02582. View

5.
Quiroga J, Galvez J, Abonia R, Insuasty B, Ortiz A, Cobo J . Highly efficient and diastereoselective synthesis of new pyrazolylpyrrolizine and pyrazolylpyrrolidine derivates by a three-component domino process. Molecules. 2014; 19(4):4284-300. PMC: 6270732. DOI: 10.3390/molecules19044284. View