I am a synthetic chemist specializing in the development of transition metal-catalyzed methodologies for the selective synthesis of structurally complex unnatural amino acids. My expertise encompasses integrating chemistry, catalysis, and radical reactions in organic synthesis to incorporate amino acids derived from tyrosine, phenylalanine, and tryptophan into peptides with site-specific modifications. Utilizing advanced techniques such as C-H functionalization, cross-coupling, macrocyclization, and amino acid stapling, I focus on site-selective aromatic modification, particularly of tyrosine, through organometallic catalysis. Additionally, I explore heterocyclic chemistry to enhance the structural and functional diversity of peptides. The overarching goal of my research is to establish versatile platforms for generating novel bioactive scaffolds with applications in protein labeling, molecular imaging, and therapeutic development. I am proficient in designing and synthesizing multi-step peptides, purification, and characterization, and possess skills in handling moisture-sensitive reactions. Furthermore, I have experience training undergraduate students in basic laboratory experiments, crafting clear academic papers with precision in citation standards, and developing convincing project proposals. During my Ph.D., I gained extensive experience in the synthesis and functionalization of amino acids such as tryptophan, phenylalanine, diketopiperazine (DKP), and natural products like protected bile acids and cholesterol. These processes involved C–H activation under transition metal catalysis, including C(sp³)-H, C(sp²)-H, and C(sp)-H activation, contributing to the advancement of methodologies for the incorporation of non-natural amino acids into peptides.
Expertise in multi-step synthesis, experience in air- and moisture-free manipulations (ie. Schlenk technique, glovebox operations). Proficient in designing and synthesizing dipeptides, tripeptides, tetrapeptides, and pentapeptides through multistep reactions using solution-phase peptide synthesis, with hands-on experience in handling anhydrous conditions; skilled in the use of coupling agents (e.g., DCC, HOBt, EDC), protecting groups (e.g., Boc, Cbz, Fmoc, Acetyl, Phthalamide) and purification and characterization techniques such as column chromatography, TLC, and NMR spectroscopy., Conducted purification of organic compounds using recrystallization, distillation, and chromatography techniques. Utilized thin-layer chromatography (TLC) for purity analysis and monitored reaction progress., Conducted high-resolution structural elucidation of organic compounds using advanced spectroscopic techniques (¹H NMR, ¹³C NMR, FTIR, UV-Vis, Mass Spectrometry)., Trained undergraduate students with basic laboratory experiments.
Prof. Rajeev Sakhuja (Thesis Supervisor)
rajeev.sakhuja@bits-pilani.ac.in
Mob No: +919950630310
Department ofChemistry
BITS Pilani, Pilani Campus
Vidya Vihar Pilani 333 031,
Rajasthan (India).
Prof. Kiran Bajaj (Thesis Co-Supervisor)
kbajaj26@gmail.com
Mob No: +918696208955
Department of Chemistry,
Amity Institute of Applied Sciences,
Amity University, Noida
Uttar Pradesh, India
Prof. Anil Kumar
anilkumar@pilani.bits-pilani.ac.in
Phone: +91-1596-515663 (Off).
Department ofChemistry
BITS Pilani, PilaniCampus
Vidya Vihar Pilani 333 031,
Rajasthan (India).
Prof. Bapurao B. Shingate
bapushingate@gmail.com
Mobile: +91985029859
Department of Chemistry
Dr. Babasaheb Ambedkar Marathwada University,
Aurangabad, Maharashtra, India