Related Experiment Video
Updated: Jan 6, 2026

Nucleoside Triphosphates - From Synthesis to Biochemical Characterization
Published on: April 3, 2014
Recent Progress in the Synthesis, Functionalization, and Biological Outlook of Pyrimidines
Glanish Jude Martis1, Praveen S Mugali2, Santosh L Gaonkar1
1Department of Chemistry, Manipal Institute of Technology, Manipal Academy of Higher Education, Manipal, Karnataka 576104, India.
None:
Pyrimidine-containing heterocyclic molecules are highly important in medicinal chemistry because of their versatile biological activities and their potential for structural modification. These scaffolds have consistently attracted the attention of chemists and biologists alike and serve as key building blocks in the design and development of bioactive compounds. Recent advances in pyrimidine chemistryincluding novel synthetic methodologies, named reactions, catalytic strategies, and functionalization techniqueshave further expanded their applicability. The biological importance of pyrimidine derivatives has been instrumental in the development of several commercially available drugs in recent years. Given the ongoing global research in this area, there is a clear need to review and highlight recent developments in a systematic manner. This review not only provides insights into current trends but also serves as a valuable resource for researchers in the pharmaceutical industry and academic institutions engaged in early-stage drug discovery efforts.
Related Concept Videos
Biosynthesis of Nucleic Acids
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Overview
Basicity of Heterocyclic Aromatic Amines
Amino Acid Biosynthetic Pathways
Phase II Reactions: Methylation Reactions
The mechanism of methylation unfolds in two stages. The first stage sees a methyltransferase enzyme facilitating the transfer of a methyl group from S-adenosylmethionine (SAM) to the substrate, forming S-adenosylhomocysteine (SAH). The second stage involves further metabolism of SAH into homocysteine, which can be recycled...

