RR
Remya Ramesh
CSIR-Indian Institute of Chemical Technology, Jubilant Biosys Ltd, National Chemical Laboratory, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill
Research areas: Chemistry · Inorganic Chemistry · Crystal structures of chemical compounds · Crystallography and molecular interactions · Crystal Structures and Properties
Employment
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CSIR-Indian Institute of Chemical Technology Scientist2021 - 2022
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Jubilant Biosys Ltd Research scientist2020 - 2021
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UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill Research associate2017 - 2019
Education
- 2011 - 2016
Projects & Funding
Projects & funding information is unavailable.
Publications (13)
- Structural Revision of the Pyrone Natural Product Syzysamalactone via Synthesis Save
- Synthesis of benzosultams via Ag(i)-catalyzed alkylative cyclization of vinyl sulfonamides Save
- Radical Cascade Annulation of Biphenyl Acrylamides to Dibenzo‐azepinones: Experimental and DFT Studies Save
- Carbonylative cyclization of biaryl enones with aldehydes and oxamic acids Save
- CAN-Promoted Thiolative ipso-Annulation of Unactivated N-Benzyl Acrylamides: Access to SCN/SCF3/SO2Ar Containing Azaspirocycles Save
- ipso-Cyclization of unactivated biaryl ynones leading to thio-functionalized spirocyclic enones Save
- Quest for Novel Chemical Entities through Incorporation of Silicon in Drug Scaffolds. Save
- Repurposing of a drug scaffold: Identification of novel sila analogues of rimonabant as potent antitubercular agents. Save
- Design, Synthesis, and Identification of Silicon Incorporated Oxazolidinone Antibiotics with Improved Brain Exposure. Save
- Silicon Incorporated Morpholine Antifungals: Design, Synthesis, and Biological Evaluation. Save
- Enantiospecific Synthesis of Both Enantiomers of the Longtailed Mealybug Pheromone and Their Evaluation in a New Zealand Vineyard. Save
- Zinc mediated allylations of chlorosilanes promoted by ultrasound: synthesis of novel constrained sila amino acids. Save
- Syntheses and determination of absolute configurations and biological activities of the enantiomers of the longtailed mealybug pheromone. Save