VN
Vasudevan Natarajan
Biocon - Bristol Myers Squibb R&D Center (BBRC, Syngene), TCG GreenChem Inc, National Chemical Laboratory, Virginia Commonwealth University
Research areas: Chemistry · Organic Chemistry · Advanced Synthetic Organic Chemistry · Innovative Microfluidic and Catalytic Techniques Innovation · Organophosphorus compounds synthesis
0000-0002-3453-986X
Employment
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Biocon - Bristol Myers Squibb R&D Center (BBRC, Syngene) Associate Scientific Director2024 - Present
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TCG GreenChem Inc Principal scientist2020 - 2023
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Virginia Commonwealth University Postdoctoral researcher2019 - 2020
Education
- 2011 - 2017
Projects & Funding
Projects & funding information is unavailable.
Publications (22)
- Development of Continuous Flow Processes to Access Pyrrolo[2,1-f][1,2,4]triazin-4-amine: An RSM for the Synthesis of Antiviral Drugs Save
- Synthesis of Chiral 1,2-Amino Alcohol-Containing Compounds Utilizing Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation of Unprotected α-Ketoamines Save
- Design and Discovery of Water-Soluble Benzooxaphosphole-Based Ligands for Hindered Suzuki–Miyaura Coupling Reactions with Low Catalyst Load Save
- Comprehensive Study on Solomonamides: Total Synthesis, Stereochemical Revision, and SAR Studies toward Identification of Simplified Lead Save
- Synthesis, biological evaluation and docking studies of silicon incorporated diarylpyrroles as MmpL3 inhibitors: An effective strategy towards development of potent anti-tubercular agents Save
- Development of a Practical Synthesis of the 8-FDC Fragment of OPC-167832 Save
- Toward a Practical, Two-Step Process for Molnupiravir: Direct Hydroxamination of Cytidine Followed by Selective Esterification Save
- Application of Vinamidinium Salt Chemistry for a Palladium Free Synthesis of Anti-Malarial MMV048: A “Bottom-Up” Approach Save
- Development of a continuous flow synthesis of FGIN-1-27 enabled by in-line 19F NMR analyses and optimization algorithms Save
- Direct C‐H arylation of indole‐3‐acetic acid derivatives enabled by an autonomous self‐optimizing flow reactor Save
- Synthesis of α-ketoamides using potassium superoxide (KO2) as an oxidizing agent Save
- A concise route to MK-4482 (EIDD-2801) from cytidine Save
- Reconfigurable Flow Platform for Automated Reagent Screening and Autonomous Optimization for Bioinspired Lignans Synthesis Save
- A multi-step continuous flow synthesis of the cystic fibrosis medicine ivacaftor Save
- Repurposing Ivacaftor for treatment of Staphylococcus aureus infections Save
- Breaking and Making of Rings: A Method for the Preparation of 4-Quinolone-3-carboxylic Acid Amides and the Expensive Drug Ivacaftor Save
- Total synthesis of deoxy-solomonamide B by mimicking biogenesis Save
- Studies toward the synthesis of potent anti-inflammatory peptides solomonamides A and B: Synthesis of a macrocyclic skeleton and key fragment 4-amino-6-(2′-amino-4′-hydroxyphenyl)-3-hydroxy-2-methyl-6- oxohexanoic acid (AHMOA) Save
- An improved process for the synthesis of ivacaftor Save
- Novel pyrrole compounds with silicon incorporation Save