Configurationally chiral SuFEx‐based polymers DD Liang, SP Pujari, M Subramaniam, M Besten, H Zuilhof Angewandte Chemie International Edition 61 (8), e202116158, 2022 | 31 | 2022 |
Copper (I) bromide catalyzed arylation of cyclic enamides and naphthyl-1-acetamides using diaryliodonium salts M Prakash, S Muthusamy, V Kesavan The Journal of Organic Chemistry 79 (17), 7836-7843, 2014 | 31 | 2014 |
Recent advances in aerobic oxidation with ruthenium catalysts S Muthusamy, N Kumarswamyreddy, V Kesavan, S Chandrasekaran Tetrahedron letters 57 (50), 5551-5559, 2016 | 30 | 2016 |
Organocatalytic Enantioselective Assembly of Spirooxindole‐naphthopyrans through Tandem Friedel–Crafts Type/Hemiketalization S Muthusamy, M Prakash, C Ramakrishnan, MM Gromiha, V Kesavan ChemCatChem 8 (9), 1708-1712, 2016 | 23 | 2016 |
Enantioselective Synthesis of Spirooxindole α‐exo‐Methylene‐γ‐butyrolactones from 3‐OBoc‐Oxindoles S Jayakumar, S Muthusamy, M Prakash, V Kesavan European Journal of Organic Chemistry 2014 (9), 1893-1898, 2014 | 15 | 2014 |
Sulfur–Phenolate Exchange: SuFEx‐Derived Dynamic Covalent Reactions and Degradation of SuFEx Polymers Y Chao, A Krishna, M Subramaniam, DD Liang, SP Pujari, ACH Sue, G Li, ... Angewandte Chemie 134 (36), e202207456, 2022 | 12 | 2022 |
Sulfur-phenolate exchange as a fluorine-free approach to S (VI) exchange chemistry on sulfonyl moieties AFJ van den Boom, M Subramaniam, H Zuilhof Organic Letters 24 (47), 8621-8626, 2022 | 8 | 2022 |
Degradable click-reaction-based polymers as highly functional materials M Subramaniam, FS Ruggeri, H Zuilhof Matter 5 (8), 2490-2492, 2022 | 4 | 2022 |
Asymmetric Cycloaddition Reactions of Oxindole α‐Keto Esters via Cascade Dienamine‐Enamine and Trienamine Strategies S Muthusamy, V Kesavan European Journal of Organic Chemistry 2019 (25), 4046-4055, 2019 | 4 | 2019 |
Enantiospecific Synthesis of Aniline-Derived Sulfonimidamides DD Liang, N Lional, B Scheepmaker, M Subramaniam, G Li, ... Organic Letters 25 (30), 5666-5670, 2023 | 2 | 2023 |
Synthesis of Large Macrocycles with Chiral Sulfur Centers via Enantiospecific SuFEx and SuPhenEx Click Reactions Y Chao, M Subramaniam, K Namitharan, Y Zhu, V Koolma, Z Hao, S Li, ... The Journal of Organic Chemistry 88 (22), 15658-15665, 2023 | 1 | 2023 |
Enantioselective Synthesis of 3‐Amino‐3’‐carbazole Oxindole Derivatives via Friedel‐Crafts Aminoalkylation Reaction S Muthusamy, N Kumarswamyreddy, V Kesavan ChemistrySelect 7 (7), e202200131, 2022 | | 2022 |