Alagiri Kaliyamoorthy - Publications
Affiliations: | 2015- | IISER Thiruvananthapuram |
Area:
Organic synthesis, natural products chemistryWebsite:
https://sites.google.com/view/alagiri-research-group/homeYear | Citation | Score | |||
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2023 | Murugesan T, Elikkottil A, Kaliyamoorthy A. Palladium-Catalyzed Regioselective C3-Allylic Alkylation of 2-Aryl Imidazopyridines with MBH Carbonates. The Journal of Organic Chemistry. 88: 2655-2665. PMID 36719167 DOI: 10.1021/acs.joc.2c03001 | 0.354 | |||
2022 | Pilathottathil F, Unnikrishnan S, Kaliyamoorthy A. Heteroarylation of Sulfenate Ions In Situ Generated from β-Sulfinyl Esters under Transition-Metal-Free Conditions. The Journal of Organic Chemistry. 87: 14980-14990. PMID 36268936 DOI: 10.1021/acs.joc.2c02153 | 0.31 | |||
2022 | Rayaroth A, Elikkottil A, Mohan Jayakumari C, Arayil Vennoli K, Vennapusa SR, Kaliyamoorthy A. Regioselective allenylation and propargylation of various -quinone methides using alkynyl azaarenes as pronucleophiles. Chemical Communications (Cambridge, England). 58: 10671-10674. PMID 36063127 DOI: 10.1039/d2cc03439e | 0.338 | |||
2021 | Murugesan T, Sivarajan C, Jayakumari CM, Singh RK, Vennapusa SR, Kaliyamoorthy A. Palladium-Catalyzed Direct C2-Biarylation of Indoles. The Journal of Organic Chemistry. PMID 34291945 DOI: 10.1021/acs.joc.1c01123 | 0.337 | |||
2020 | Rayaroth A, Singh RK, A V K, Hari K, Kaliyamoorthy A. Base-promoted 1,6-conjugate addition of alkylazaarenes to para-quinone methides. Organic & Biomolecular Chemistry. PMID 32307478 DOI: 10.1039/D0Ob00419G | 0.505 | |||
2020 | Pilathottathil F, Vineet Kumar D, Kaliyamoorthy A. Synthesis of various acylating agents directly from carboxylic acids Synthetic Communications. 50: 1622-1632. DOI: 10.1080/00397911.2020.1747631 | 0.389 | |||
2019 | Jayakrishnan K, Tamilarasu M, Jincy K, Kaliyamoorthy A. N-Heterocyclic carbene as a Brønsted base catalyst for the amination of naphthol derivatives and alcoholysis of glutaric anhydrides Tetrahedron Letters. 60: 151131. DOI: 10.1016/J.Tetlet.2019.151131 | 0.084 | |||
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