| Year |
Citation |
Score |
| 2025 |
Sahu S, Paikin ZE, Talbott JM, Czabala P, Raj M. Coarctate reaction for synthesis of fluorescent N-heterocycles, late-stage functionalization, and photo-triggered drug delivery. Nature Communications. 16: 3780. PMID 40263307 DOI: 10.1038/s41467-025-59057-x |
0.318 |
|
| 2024 |
Karan G, Sahu S, Metya A, Maji MS. Asymmetric 1,2-Migration on Vicinal Tetrasubstituted Stereocenters Constructed from α-Keto Imines. Angewandte Chemie (International Ed. in English). e202405212. PMID 38721919 DOI: 10.1002/anie.202405212 |
0.703 |
|
| 2023 |
Ghosh M, Sahu S, Saha S, Maji MS. Construction of C2-indolyl-quaternary centers by branch-selective allylation: enabling concise total synthesis of the (±)-mersicarpine alkaloid. Chemical Science. 15: 1789-1795. PMID 38303951 DOI: 10.1039/d3sc04732f |
0.742 |
|
| 2022 |
Sahu S, Banerjee A, Kundu S, Bhattacharyya A, Maji MS. Synthesis of functionalized indoles cascade benzannulation strategies: a decade's overview. Organic & Biomolecular Chemistry. 20: 3029-3042. PMID 35332905 DOI: 10.1039/d2ob00187j |
0.632 |
|
| 2022 |
Sahu S, Karan G, Roy L, Maji MS. An expeditious route to sterically encumbered nonproteinogenic α-amino acid precursors using allylboronic acids. Chemical Science. 13: 2355-2362. PMID 35310508 DOI: 10.1039/d1sc06259j |
0.771 |
|
| 2021 |
Karan G, Sahu S, Maji MS. A one-pot "back-to-front" approach for the synthesis of benzene ring substituted indoles using allylboronic acids. Chemical Communications (Cambridge, England). PMID 33908966 DOI: 10.1039/d1cc01512e |
0.79 |
|
| 2019 |
Sahu S, Roy A, Gorai M, Guria S, Sudan Maji M. C3-Alkenylation between Pyrroles and Aldehydes Mediated by a Brønsted Acid and a Brønsted Base European Journal of Organic Chemistry. 2019: 6396-6400. DOI: 10.1002/Ejoc.201901228 |
0.39 |
|
| 2018 |
Sahu S, Das B, Maji MS. 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. PMID 30336678 DOI: 10.1021/Acs.Orglett.8B02804 |
0.775 |
|
| 2017 |
Sahu S, Banerjee A, Maji MS. Transition-Metal-Free Redox-Neutral One-Pot C3-Alkenylation of Indoles Using Aldehydes. Organic Letters. PMID 28080068 DOI: 10.1021/Acs.Orglett.6B03612 |
0.781 |
|
| 2017 |
Banerjee A, Sahu S, Maji MS. Benzannulation of 2-Alkenylindoles using Aldehydes by Sequential Triple-Relay Catalysis: A Route to Carbazoles and Carbazole Alkaloids Advanced Synthesis & Catalysis. 359: 1860-1866. DOI: 10.1002/Adsc.201700092 |
0.766 |
|
| 2014 |
Kotha SS, Chandrasekar S, Sahu S, Sekar G. Iron-TEMPO-catalyzed domino aerobic alcohol oxidation/oxidative cross-dehydrogenative coupling for the synthesis of α-keto amides European Journal of Organic Chemistry. 2014: 7451-7457. DOI: 10.1002/Ejoc.201402961 |
0.38 |
|
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