Soham Maity
Affiliations: | 2017-2019 | Yale University, New Haven, CT |
Area:
Organic synthesis, catalysis, methodologyGoogle:
"Soham Maity"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Debabrata Maiti | grad student | 2011-2016 | IIT Bombay |
| Jonathan A. Ellman | post-doc | 2017-2019 | Yale |
| Shannon S. Stahl | post-doc | 2019-2021 | UW Madison |
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Publications
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| Maity S, Lopez MA, Bates DM, et al. (2023) Polar Heterobenzylic C(sp)-H Chlorination Pathway Enabling Efficient Diversification of Aromatic Nitrogen Heterocycles. Journal of the American Chemical Society |
| Paul N, Maity S, Panja S, et al. (2021) Recent Advances in the Nitration of Olefins. Chemical Record (New York, N.Y.) |
| Maity S, Potter TJ, Ellman JA. (2019) α-Branched amines by catalytic 1,1-addition of C-H bonds and aminating agents to terminal alkenes. Nature Catalysis. 2: 756-762 |
| Baccalini A, Vergura S, Dolui P, et al. (2019) Cobalt-Catalyzed C(sp)-H Allylation of Biphenyl Amines with Unbiased Terminal Olefins. Organic Letters |
| Agasti S, Maiti S, Maity S, et al. (2019) Bismuth nitrate as a source of nitro radical in ipso-nitration of carboxylic acids Polyhedron. 172: 120-124 |
| Boerth JA, Maity S, Williams SK, et al. (2018) Selective and synergistic cobalt(III)-catalyzed three-component C-H bond addition to dienes and aldehydes. Nature Catalysis. 1: 673-679 |
| Thrimurtulu N, Khan S, Maity S, et al. (2017) Palladium catalyzed direct aliphatic γC(sp(3))-H alkenylation with alkenes and alkenyl iodides. Chemical Communications (Cambridge, England) |
| Maity S, Dolui P, Kancherla R, et al. (2017) Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction. Chemical Science. 8: 5181-5185 |
| Gholap AVA, Maity S, Schulzke C, et al. (2017) Synthesis of Cu-catalysed quinazolinones using a Csp3-H functionalisation/cyclisation strategy. Organic & Biomolecular Chemistry |
| Maity S, Hoque E, Dhawa U, et al. (2016) Palladium catalyzed selective distal C-H olefination of biaryl systems. Chemical Communications (Cambridge, England) |