Multicomponent reactions have gained significant importance as a tool for the synthesis of a wide variety of useful compounds, including pharmaceuticals. In this context, the multiple component approach is especially appealing in view of the fact that products are formed in a single step, and the diversity can be readily achieved simply by varying the reacting components. The eco-friendly, solvent-free multicomponent approach opens up numerous possibilities for conducting rapid organic synthesis and functional group transformations more efficiently. Additionally, there are distinct advantages of these solvent-free protocols since they provide reduction or elimination of solvents thereby preventing pollution in organic synthesis “at source”. The chemo-, regio- or stereoselective synthesis of high-value chemical entities and parallel synthesis to generate a library of small molecules will add to the growth of multicomponent solvent-free reactions in the near future. In this review we summarized the results reported mainly within the last 10 years. It is quite clear from the growing number of emerging publications in this field that the possibility to utilize multicomponent technology allows reaction conditions to be accessed that are very valuable for organic synthesis. Therefore, diversity oriented synthesis (DOS) is rapidly becoming one of the paradigms in the process of modern drug discovery. This has spurred research in those fields of chemical investigation that lead to the rapid assembly of not only molecular diversity, but also molecular complexity. As a consequence multi-component as well as domino or related reactions are witnessing a new spring.

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Recent developments in solvent-free multicomponent reactions: a perfect synergy for eco-compatible organic synthesis

An efficient one-pot synthesis of spirooxindole derivatives by three-component reaction of isatins, malononitrile (cyanoacetic ester) and 1,3-dicarbonyl compounds in water in the presence of l-proline is reported This new protocol has the advantages of environmental friendliness, higher yields, shorter reaction times, low cost, and convenient operation

Efficient one-pot synthesis of spirooxindole derivatives catalyzed by L-proline in aqueous medium.

Solvent-free multicomponent synthesis of pyranopyrazoles: per-6-amino-β-cyclodextrin as a remarkable catalyst and host

Eco-friendly synthesis and biological evaluation of substituted pyrano[2,3-c]pyrazoles

A novel and efficient one-pot synthesis of spiro[indoline-3,4′-pyrazolo[3,4-b]quinoline]dione, spiro[furo[3,4-e]pyrazolo[3,4-b]pyridine-4,3′-indoline]dione, and spiro[indeno[2,1-e]pyrazolo[3,4-b]pyridine-4,3′-indoline]dione derivatives via three-component reaction of isatin, 5-amino-3-methylpyrazole, and 1,3-dicarbonyl compounds in aqueous medium is described. The advantages of this method include high efficiency, mild reaction conditions, convenient operation, and environmentally benign conditions.

Efficient One-Pot Synthesis of Novel Spirooxindole Derivatives via Three-Component Reaction in Aqueous Medium

Three‐Component One‐Pot Synthesis of 1,4‐Dihydropyrano[2,3‐c]pyrazole Derivatives in Aqueous Media

l-Proline-derived tertiary amino alcohol as a new chiral ligand for enantioselective alkynylation of aldehydes

A series of 2-amino-4-aryl-5-oxo-4,5-dihydropyrano[3,2-c]chromene derivatives has been synthesised by the reaction of 4-hydroxycoumarin and substituted cinnamonitriles catalysed by KF-montmorillonite. The structures were characterised by IR and 1 H NMR spectroscopic data and confirmed by X-ray diffraction analysis.

Synthesis of 2-amino-4-aryl-5-oxo-4,5-dihydropyrano[3,2-c] chromene derivatives catalysed by KF-montmorillonite

The title compound, C20H14N2O4·C3H7NO, was synthesized by the reaction of 4-hydroxy­coumarin and 4′-methoxy­benzyl­idene­malono­nitrile catalyzed by KF-montmorillonite. There are two independent mol­ecules in the asymmetric unit, and the amino groups form N—H⋯O hydrogen bonds with N,N-di­methyl­form­amide.

2‐Amino‐4‐(4‐methoxy­phenyl)‐5‐oxo‐4H,5H‐pyrano­[3,2‐c]­chromene‐3‐carbo­nitrile N,N‐di­methyl­form­amide solvate

A range of unsymmetrical and symmetrical disiloxanes have been effectively synthesized through oxidative coupling of hydrosilanes with DMF as a source of oxygen catalyzed by 0.5% AgNTf2 at 60 oC....

Nan Wu

Papers

Three‐Component One‐Pot Synthesis of 1,4‐Dihydropyrano[2,3‐c]pyrazole Derivatives in Aqueous Media

l-Proline-derived tertiary amino alcohol as a new chiral ligand for enantioselective alkynylation of aldehydes

Synthesis of 2-amino-4-aryl-5-oxo-4,5-dihydropyrano[3,2-c] chromene derivatives catalysed by KF-montmorillonite

2‐Amino‐4‐(4‐methoxyphenyl)‐5‐oxo‐4H,5H‐pyrano[3,2‐c]chromene‐3‐carbonitrile N,N‐dimethylformamide solvate

Silver(I)-Catalyzed Oxidative Coupling of Hydrosilanes with DMF to Symmetrical and Unsymmetrical Disiloxanes

Nan Wu

Papers

Three‐Component One‐Pot Synthesis of 1,4‐Dihydropyrano[2,3‐c]pyrazole Derivatives in Aqueous Media

l-Proline-derived tertiary amino alcohol as a new chiral ligand for enantioselective alkynylation of aldehydes

Synthesis of 2-amino-4-aryl-5-oxo-4,5-dihydropyrano[3,2-c] chromene derivatives catalysed by KF-montmorillonite

2‐Amino‐4‐(4‐methoxy­phenyl)‐5‐oxo‐4H,5H‐pyrano­[3,2‐c]­chromene‐3‐carbo­nitrile N,N‐di­methyl­form­amide solvate

Silver(I)-Catalyzed Oxidative Coupling of Hydrosilanes with DMF to Symmetrical and Unsymmetrical Disiloxanes

2‐Amino‐4‐(4‐methoxyphenyl)‐5‐oxo‐4H,5H‐pyrano[3,2‐c]chromene‐3‐carbonitrile N,N‐dimethylformamide solvate