Year |
Citation |
Score |
2024 |
Pramanik S, Das AK, Debnath S, Maity S. Introducing Alkyl Selenocyanates as Bifunctional Reagents in Photoredox Catalysis: Divergent Access to Ambident Isomers of -SeCN. Organic Letters. PMID 39172107 DOI: 10.1021/acs.orglett.4c02430 |
0.59 |
|
2024 |
Hoque IU, Samanta A, Pramanik S, Chowdhury SR, Lo R, Maity S. Photocascade chemoselective controlling of ambident thio(seleno)cyanates with alkenes via catalyst modulation. Nature Communications. 15: 5739. PMID 38982050 DOI: 10.1038/s41467-024-49279-w |
0.436 |
|
2024 |
Pramanik S, Samanta A, Maity S. A two carbon homologation of Friedel-Crafts alkylation enabled by photochemical alkene stitching: modular assembly of cyclolignans. Chemical Communications (Cambridge, England). 60: 5282-5285. PMID 38656305 DOI: 10.1039/d4cc00957f |
0.624 |
|
2023 |
Pramanik S, Mondal PP, Maity S. Organo-photoredox-Catalyzed Selective Mono- and Bis-C-H Alkylation of Electron-Rich (Hetero)Arenes. The Journal of Organic Chemistry. PMID 37823605 DOI: 10.1021/acs.joc.3c01757 |
0.592 |
|
2023 |
Singh D, Pramanik S, Maity S. Photocatalytic sequential C-H functionalization expediting acetoxymalonylation of imidazo heterocycles. Beilstein Journal of Organic Chemistry. 19: 666-673. PMID 37205129 DOI: 10.3762/bjoc.19.48 |
0.604 |
|
2022 |
Samanta A, Pramanik S, Mondal S, Maity S. Zinc acetate-promoted blocking of the ATRA process with alkyl halides enabling photochemical alkylamination of olefins. Chemical Communications (Cambridge, England). 58: 8400-8403. PMID 35796040 DOI: 10.1039/d2cc02574d |
0.629 |
|
2019 |
Jash M, De S, Pramanik S, Chowdhury C. Palladium(II)-Catalyzed Cascade Reactions of Ene-Ynes Tethered to Cyano/Aldehyde: Access to Naphtho[1,2- b]furans and Benzo[ g]indoles. The Journal of Organic Chemistry. PMID 31241931 DOI: 10.1021/acs.joc.9b00861 |
0.343 |
|
2019 |
Singh K, Pramanik S, Hamlin TA, Mondal B, Das D, Saha J. Lewis acid catalyzed annulation of spirocyclic donor-acceptor cyclopropanes with exo-heterocyclic olefins: access to highly functionalized bis-spirocyclopentane oxindole frameworks. Chemical Communications (Cambridge, England). PMID 31147663 DOI: 10.1039/C9Cc03393A |
0.332 |
|
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