SC
Sayanti Chatterjee
Max Planck Institute for Chemical Energy Conversion, Indian Institute of Technology Roorkee, Max-Planck-Institut für Kohlenforschung
Employment
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Max Planck Institute for Chemical Energy Conversion Postdoctoral Research Fellow2020 - Present
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Max-Planck-Institut für Kohlenforschung Postdoctoral Research Fellow2018 - 2020
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University of Virginia Postdoctoral Research Associate2017 - 2018
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Indian Institute of Technology Roorkee Assistant Professor
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (25)
- Unveiling the Potential of p-Block Bismuth in Homogeneous Electrocatalytic Proton Reduction: Secondary Coordination Sphere Control of Catalytic Activity Save
- Mechanistic Insights into the Reductive N–O Bond Cleavage of O-Acyl Hydroxylamines: Dual Reactivity as Potent Oxidants and Nitrogen Transfer Agents Save
- An Iron‐Catalyzed Sustainable Functional Group Transfer Strategy for In‐Water Transformation of Organic Sulfides to Sulfoxides by a Hydroxylamine‐Derived Oxidant Save
- Cooperative Sulfur Transformations at a Dinickel Site: A Metal Bridging Sulfur Radical and Its H-Atom Abstraction Thermochemistry Save
- First row transition metal catalyzed small molecule activation for sustainable organic transformation: Synergy between nature and chemist’s toolbox Save
- In Solution Identification of the Lysine–Cysteine Redox Switch with a NOS Bridge in Transaldolase by Sulfur K-Edge X-ray Absorption Spectroscopy Save
- Dioxygen Reduction and Bioinspired Oxidations by Non-heme Iron(II)−α-Hydroxy Acid Complexes Save
- Cu4S Cluster in “0-Hole” and “1-Hole” States: Geometric and Electronic Structure Variations for the Active CuZ* Site of N2O Reductase Save
- A Combined Spectroscopic and Computational Study on the Mechanism of Iron-Catalyzed Aminofunctionalization of Olefins Using Hydroxylamine Derived N–O Reagent as the “Amino” Source and “Oxidant” Save
- Hydroxylamin‐abgeleitetes Reagenz als duales Oxidationsmittel und Aminogruppendonor für die eisenkatalysierte Herstellung von ungeschützten Sulfinamiden aus Thiolen Save