Modhu Sudan Maji, PhD
Affiliations: | Technische Universität Berlin, Berlin, Berlin, Germany | ||
2013- | Chemistry | Indian Institute of Technology Kharagpur |
Area:
Heterocycle Chemistry, Alkaloids Total Synthesis, C-H Bond Functionalization, PAHWebsite:
https://www.msmlabiitkgp.com/msmGoogle:
"Modhu Sudan Maji"Mean distance: 8.71 | S | N | B | C | P |
Parents
Sign in to add mentorGoverdhan Mehta | research assistant | 2005-2006 | Indian Institute of Science, Bangalore, India | |
(Did my MS thesis work) | ||||
Armido Studer | grad student | 2006-2010 | Westfälische Wilhelms-Universität Münster | |
(Member of the Graduate School of Chemistry) | ||||
Magnus Rueping | post-doc | 2010-2013 | RWTH Aachen University | |
(I was AvH Fellow) | ||||
Martin Oestreich | post-doc | 2013-2013 | TU Berlin |
Children
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Publications
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Sk MR, Bhattacharyya A, Saha S, et al. (2023) Annulative π-Extension by Rh(III)-Catalyzed Ketone-Directed C-H Activation: Rapid Access to Pyrenes and Related PAHs. Angewandte Chemie (International Ed. in English). e202305258 |
Kundu S, Roy L, Maji MS. (2022) Development of Carbazole-Cored Organo-Photocatalyst for Visible Light-Driven Reductive Pinacol/Imino-Pinacol Coupling. Organic Letters |
Saha S, Maji MS. (2022) Cp*Co(III)-catalyzed thiocarbamate-directed C-H aminocarbonylation, amination, and cascade annulation of pyrroles. Chemical Communications (Cambridge, England). 58: 10865-10868 |
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 |
Banerjee A, Saha S, Maji MS. (2022) Cascade Benzannulation Approach for the Syntheses of Lipocarbazoles, Carbazomycins, and Related Alkaloids. The Journal of Organic Chemistry. 87: 4343-4359 |
Kundu S, Banerjee A, Pal SC, et al. (2021) Cascade annulative π-extension for the rapid construction of carbazole based polyaromatic hydrocarbons. Chemical Communications (Cambridge, England) |
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) |
Mondal H, Sk MR, Maji MS. (2020) Cooperativity within the catalyst: alkoxyamide as a catalyst for bromocyclization and bromination of (hetero)aromatics. Chemical Communications (Cambridge, England) |
Bera SS, Maji MS. (2020) Carbamates: A Directing Group for Selective C-H Amidation and Alkylation under Cp*Co(III) Catalysis. Organic Letters. 22: 2615-2620 |