Surojit Santra
Affiliations: | 2013- | IACS Kolkata |
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Publications
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Santra S, Maji U, Guin J. (2020) Enantioselective α-Amination of Acyclic 1,3-Dicarbonyls Catalyzed by N-Heterocyclic Carbene. Organic Letters |
Porey A, Santra S, Guin J. (2019) Highly enantioselective synthesis of functionalized glutarimide using oxidative N-heterocyclic carbene catalysis: a formal synthesis of (-)-paroxetine. The Journal of Organic Chemistry |
Santra S, Porey A, Jana B, et al. (2018) N-Heterocyclic carbenes as chiral Brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction. Chemical Science. 9: 6446-6450 |
Kopchuk DS, Nikonov IL, Khasanov AF, et al. (2018) Studies on the interactions of 5-R-3-(2-pyridyl)-1,2,4-triazines with arynes: inverse demand aza-Diels-Alder reaction versus aryne-mediated domino process. Organic & Biomolecular Chemistry |
Santra S, Porey A, Guin J. (2018) 1,6-Conjugate Addition of 1,3-Dicarbonyl Compounds topara-Quinone Methides Enabled by Noncovalent N-Heterocyclic Carbene Catalysis Asian Journal of Organic Chemistry. 7: 477-486 |
Sau P, Santra SK, Rakshit A, et al. (2017) Tert-Butyl Nitrite Mediated Domino Synthesis of Isoxazolines and Isoxazoles from Terminal Aryl Alkenes and Alkynes. The Journal of Organic Chemistry |
Santra SK, Banerjee A, Rajamanickam S, et al. (2016) Pd(II)/CuBr2 catalysed keto α-Csp3-H benzoxylation of N,N-dialkylamides directed by o-hydroxy groups. Chemical Communications (Cambridge, England) |
Porey A, Santra S, Guin J. (2016) Direct N-Acylation of Sulfoximines with Aldehydes by N-Heterocyclic Carbene Catalysis under Oxidative Conditions Asian Journal of Organic Chemistry. 5: 870-873 |
Rajamanickam S, Majji G, Santra SK, et al. (2015) Bu4NI Catalyzed C-N Bond Formation via Cross-Dehydrogenative Coupling of Aryl Ethers (Csp3-H) and Tetrazoles (N-H). Organic Letters |
Santra S, Guin J. (2015) Enhanced Reactivity of Aerobic Diimide Olefin Hydrogenation with Arylboronic Compounds: An Efficient One-Pot Reduction/Oxidation Protocol European Journal of Organic Chemistry. 2015: 7253-7257 |