Somraj Guha
Affiliations: | 2016 | IIT Madras |
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Parents
Sign in to add mentor| Uli kazmaier | grad student | ||
| Lutz Friedjan Tietze | grad student | ||
| G. Sekar | grad student | 2016 | IIT Madras |
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Publications
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| Hoi DM, Junker S, Junk L, et al. (2023) Clp-targeting BacPROTACs impair mycobacterial proteostasis and survival. Cell. 186: 2176-2192.e22 |
| Morreale FE, Kleine S, Leodolter J, et al. (2022) BacPROTACs mediate targeted protein degradation in bacteria. Cell |
| Guha S, Kazi I, Sathish D, et al. (2022) Iodine-Promoted Controlled and Selective Oxidation of (Aryl)(Heteroaryl)Methanes. The Journal of Organic Chemistry. 87: 5424-5429 |
| Nandy A, Kazi I, Guha S, et al. (2021) Visible-Light-Driven Halogen-Bond-Assisted Direct Synthesis of Heteroaryl Thioethers Using Transition-Metal-Free One-Pot C-I Bond Formation/C-S Cross-Coupling Reaction. The Journal of Organic Chemistry. 86: 2570-2581 |
| Guha S, Senthilkumar S, Voß E, et al. (2020) Aldosterone Glucuronide, an Important Biomarker: Synthesis and Structure Elucidation of Novel Isomers. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Sundaravelu N, Guha S, Sekar G. (2020) Iodonium Ion-Catalyzed Domino Synthesis of -Selective α,β-Diphenylthio Enones from Easily Accessible Secondary Alcohols. The Journal of Organic Chemistry. 85: 5895-5906 |
| Kazi I, Guha S, Sekar G. (2019) Halogen Bond-Assisted Electron-Catalyzed Atom Economic Iodination of Heteroarenes at Room Temperature. The Journal of Organic Chemistry. 84: 6642-6654 |
| Prasanna R, Guha S, Sekar G. (2019) Proton-Coupled Electron Transfer: Transition-Metal-Free Selective Reduction of Chalcones and Alkynes Using Xanthate/Formic Acid. Organic Letters. 21: 2650-2653 |
| Guha S, Sekar G. (2018) Metal-free Halogen(I) Catalysts for Oxidation of (Aryl)(heteroaryl)-methanes to Ketones or Esters : Selectivity Control by Halogen Bond. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Guha S, Kazi I, Mukherjee P, et al. (2017) Halogen-bonded iodonium ion catalysis: a route to α-hydroxy ketones via domino oxidations of secondary alcohols and aliphatic C-H bonds with high selectivity and control. Chemical Communications (Cambridge, England) |