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Sign in to add mentorModhu Sudan Maji | grad student | 2014- | Indian Institute of Technology Kharagpur |
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Sahu S, Paikin ZE, Talbott JM, et al. (2025) Coarctate reaction for synthesis of fluorescent N-heterocycles, late-stage functionalization, and photo-triggered drug delivery. Nature Communications. 16: 3780 |
Karan G, Sahu S, Metya A, et al. (2024) Asymmetric 1,2-Migration on Vicinal Tetrasubstituted Stereocenters Constructed from α-Keto Imines. Angewandte Chemie (International Ed. in English). e202405212 |
Ghosh M, Sahu S, Saha S, et al. (2023) Construction of C2-indolyl-quaternary centers by branch-selective allylation: enabling concise total synthesis of the (±)-mersicarpine alkaloid. Chemical Science. 15: 1789-1795 |
Sahu S, Banerjee A, Kundu S, et al. (2022) Synthesis of functionalized indoles cascade benzannulation strategies: a decade's overview. Organic & Biomolecular Chemistry. 20: 3029-3042 |
Sahu S, Karan G, Roy L, et al. (2022) An expeditious route to sterically encumbered nonproteinogenic α-amino acid precursors using allylboronic acids. Chemical Science. 13: 2355-2362 |
Karan G, Sahu S, Maji MS. (2021) A one-pot "back-to-front" approach for the synthesis of benzene ring substituted indoles using allylboronic acids. Chemical Communications (Cambridge, England) |
Sahu S, Roy A, Gorai M, et al. (2019) C3-Alkenylation between Pyrroles and Aldehydes Mediated by a Brønsted Acid and a Brønsted Base European Journal of Organic Chemistry. 2019: 6396-6400 |
Sahu S, Das B, Maji MS. (2018) Stereodivergent Total Synthesis of Hapalindoles, Fischerindoles, Hapalonamide H, and Ambiguine H Alkaloids by Developing a Biomimetic, Redox-Neutral, Cascade Prins-Type Cyclization. Organic Letters. 20: 6485-6489 |
Sahu S, Banerjee A, Maji MS. (2017) Transition-Metal-Free Redox-Neutral One-Pot C3-Alkenylation of Indoles Using Aldehydes. Organic Letters |
Banerjee A, Sahu S, Maji MS. (2017) Benzannulation of 2-Alkenylindoles using Aldehydes by Sequential Triple-Relay Catalysis: A Route to Carbazoles and Carbazole Alkaloids Advanced Synthesis & Catalysis. 359: 1860-1866 |