Polymer based advanced recipes for imidazoles: a review.

Imidazoles and their scaffold are an extraordinarily essential class of nitrogen bearing azole heterocyclic compounds. They have different place in wide area of organic synthesis, which can be utilized in a variety of applications in diverse fields including agriculture, medicine, polymer and various industries. Numerous methods for synthesis of imidazole derivatives are reported in last few decades. Existing conventional methods are more or less significant and confined due to its time-consuming reactions, high cost of catalyst, extensive methodologies, low yield rate or no reusability respectively. Overcoming to inefficient conventional methods, finding of novel and effective methods of imidazole synthesis becomes a crucial step in expanding dynamics of material chemistry. The synthesis and design of imidazole derivatives employing polymer-supported techniques will be discussed in this review. In addition, the utilization of polymer-supported organic, inorganic, hybrid, bio, and nanocatalysts in the synthesis process will be discussed.

Advances in polymer based Friedlander quinoline synthesis.

Nitrogen containing heterocyclic compounds has acquired their remarkable and distinct place in the wide area of organic synthesis due to the broad range of applications. Among them, quinoline motifs have attracted researchers in the synthetic chemistry because of its presence in the large number of pharmacologically active compounds. Different methods for synthesis of quinoline derivatives are reported, among them the Friedlander synthesis have provided comparatively more efficient approach. Many of the reported conventional Friedlander methodologies have some problems such as difficult product isolation procedures, poor yields and use of expensive catalysts, etc. Recently, polymer or solid supported synthetic approaches have attracted the attention of researchers because of their easy execution, greater selectivity, increased product yields, simple work-up procedures, recoverability and reusability of the catalysts. In consideration with the advantages of polymer supported synthetic strategies, the proposed review covers the role of polymers in the Friedlander synthesis; which may use polymers of organic, inorganic or hybrid in nature and of nanolevel as well.

Biginelli Reaction: Polymer Supported Catalytic Approaches.

The Biginelli product, dihydropyrimidinone (DHPM) core, and its derivatives are of immense biological importance. There are several methods reported as modifications to the original Biginelli reaction. Among them, many involve the use of different catalysts. Also, among the advancements that have been made to the Biginelli reaction, improvements in product yields, less hazardous reaction conditions, and simplified isolation of products from the reaction predominate. Recently, solid-phase synthetic protocols have attracted the research community for improved yields, simplified product purification, recyclability of the solid support, which forms a special economic approach for Biginelli reaction. The present Review highlights the role of polymer-supported catalysts in Biginelli reaction, which may involve organic, inorganic, or hybrid polymers as support for catalysts. A few of the schemes involve magnetically recoverable catalysts where work up provides green approach relative to traditional methods. Some research groups used polymer-catalyst nanocomposites and polymer-supported ionic liquids as catalyst. Solvent-free, an ultrasound or microwave-assisted Biginelli reactions with polymer-supported catalysts are also reported.