Role of Click Chemistry in Organic Synthesis

Click chemistry involves highly efficient organic reactions of two or more highly functionalized chemical entities under eco-benign conditions for the synthesis of different heterocycles. Several organic reactions such as nucleophilic ring-opening reactions, cyclo-additions, nucleophilic addition reactions, thiol-ene reactions, Diels Alder reactions, etc. are included in click reactions. These reactions have very important features i.e. high functional group tolerance, formation of a single product, high atom economy, high yielding, no need for column purification, etc. It also possesses several applications in drug discovery, supramolecular chemistry, material science, nanotechnology, etc. Being highly significant and valuable, we have elaborated on several aspects of click reactions in organic synthesis in this chapter. Recent advancements in the field of organic synthesis using click chemistry approach have been deliberated by citing last five years articles

Metal Catalyzed Oxidation Reactions of Alkenes Using Eco-Friendly Oxidants

Oxidation of alkenes is an important reaction in academia, industry and science as it is used to develop epoxides, carbonyls, allylic compounds, 1,2-diols, etc. Metal catalyzed oxidation of alkenes has aroused as a significant tool in modern organic synthesis. Several techniques are available; however some of them suffer from few shortcomings viz. high cost, toxic nature, harsh reaction condition, solid waste generation, etc. In view of these drawbacks, green oxidants i.e. O2, H2O2, TBHP, etc. have shown noteworthy prospects due to their nature, low cost, high atom economy and high sustainability in metal catalyzed reactions. This chapter highlights the metal catalyzed green oxidation of alkenes and shall provide new strategies for the functionalization and transformation of alkenes

Pioneering Synthetic Strategies of 2-Substituted Benzothiazoles Using 2-Aminothiophenol

Heterocycles, compounds featuring heteroatoms like nitrogen, sulfur, and oxygen, are integral in fields such as synthesis, pharmacology, and medicine. Among these, benzothiazoles, formed by fusing thiazole with benzene, hold significant prominence. Their unique reactivity, especially at the carbon position between nitrogen and sulfur, has sparked wide interest. Notably, 2-substituted benzothiazoles exhibit diverse biological activities, including anticonvulsant, antimicrobial, and antioxidant properties, making them valuable in drug discovery. This review unveils an array of mesmerizing methods employed by chemists to prepare these compounds using 2-aminothiophenol as one of the precursors with other varied reactants. From novel strategies to sophisticated methodologies, each section of this review provides a glimpse into the fascinating world of synthetic chemistry of 2-substituted benzothiazoles. Delving into the diverse synthetic applications of 2-substituted benzothiazoles, this paper not only enriches our understanding of their synthesis but also sparks the imagination with the possibilities for future advancements

Facile One Pot Synthesis of Acridinediones Using Caffeine Hydrogen Sulfate Catalyst and Their Antimicrobial Evaluation

A facile approach for the synthesis of bioactive acridinedione analogs using dimedone, aryl aldehydes, and ammonium acetate was developed using caffeine hydrogen sulfate catalyst in ethanol and water (2:1) solvent mixture at room temperature. The significant advantages of this procedure are efficient and simple method, ambient conditions, short reaction time (5–30 min), simple workup, easily recoverable catalyst, broad substrate scope and good yields (45–80%). Being water soluble, the catalyst was easily recovered by water and reused up to 4 runs. Moreover, the antimicrobial profile of synthesized derivatives was performed against different bacterial and fungal strains using broth microdilution method. Most of the synthesized derivatives exhibited significant activity against bacterial and fungal strains compared to standard. Compounds 4e (31.25 µg/mL and 31.25 µg/mL) and 4g (31.25 µg/mL and 62.5 µg/mL) were found the most active against E. coli. and S. aureus respectively with good MIC values. Compound 4f and 4j displayed the highest antifungal activity against A. niger with 31.25 µg/mL MIC value. </p