N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions S Murarka Advanced Synthesis & Catalysis 360 (9), 1735-1753, 2018 | 347 | 2018 |
Catalytic enantioselective intramolecular redox reactions: Ring-fused tetrahydroquinolines S Murarka, I Deb, C Zhang, D Seidel Journal of the American Chemical Society 131 (37), 13226-13227, 2009 | 234 | 2009 |
Lewis acid catalyzed formation of tetrahydroquinolines via an intramolecular redox process S Murarka, C Zhang, MD Konieczynska, D Seidel Organic Letters 11 (1), 129-132, 2009 | 206 | 2009 |
Single Electron Transfer-Induced Redox Processes Involving N-(Acyloxy)phthalimides SK Parida, T Mandal, S Das, SK Hota, S De Sarkar, S Murarka ACS Catalysis 11 (3), 1640-1683, 2021 | 198 | 2021 |
Facile formation of cyclic aminals through a Brønsted acid-promoted redox process C Zhang, S Murarka, D Seidel The Journal of Organic Chemistry 74 (1), 419-422, 2009 | 192 | 2009 |
Identification of pyrazolopyridazinones as PDEδ inhibitors B Papke, S Murarka, HA Vogel, P Martín-Gago, M Kovacevic, DC Truxius, ... Nature communications 7 (1), 11360, 2016 | 165 | 2016 |
Phenyl hydrazine as initiator for direct arene C–H arylation via base promoted homolytic aromatic substitution A Dewanji, S Murarka, DP Curran, A Studer Organic letters 15 (23), 6102-6105, 2013 | 123 | 2013 |
A PDE6δ‐KRas inhibitor chemotype with up to seven H‐bonds and picomolar affinity that prevents efficient inhibitor release by Arl2 P Martín‐Gago, EK Fansa, CH Klein, S Murarka, P Janning, M Schürmann, ... Angewandte Chemie 129 (9), 2463-2468, 2017 | 93 | 2017 |
Structure guided design and kinetic analysis of highly potent benzimidazole inhibitors targeting the PDEδ prenyl binding site G Zimmermann, C Schultz-Fademrecht, P Küchler, S Murarka, S Ismail, ... Journal of medicinal chemistry 57 (12), 5435-5448, 2014 | 82 | 2014 |
Covalent protein labeling at glutamic acids P Martín-Gago, EK Fansa, M Winzker, S Murarka, P Janning, ... Cell chemical biology 24 (5), 589-597. e5, 2017 | 81 | 2017 |
Late stage functionalization of heterocycles using hypervalent iodine (III) reagents R Budhwan, S Yadav, S Murarka Organic & Biomolecular Chemistry 17 (26), 6326-6341, 2019 | 76 | 2019 |
Zinc triflate catalyzed aerobic cross-dehydrogenative coupling (CDC) of alkynes with nitrones: a new entry to isoxazoles S Murarka, A Studer Organic Letters 13 (10), 2746-2749, 2011 | 70 | 2011 |
Transition-Metal-Free Sonogashira-Type Coupling of ortho-Substituted Aryl and Alkynyl Grignard Reagents by Using 2,2,6,6-Tetramethylpiperidine-N-oxyl Radical … MS Maji, S Murarka, A Studer Organic letters 12 (17), 3878-3881, 2010 | 67 | 2010 |
Multicomponent Synthesis of Biologically Relevant S-Aryl Dithiocarbamates Using Diaryliodonium Salts SK Parida, S Jaiswal, P Singh, S Murarka Organic Letters 23 (16), 6401-6406, 2021 | 52 | 2021 |
Transition Metal‐Free TEMPO‐Catalyzed Oxidative Cross‐Coupling of Nitrones with Alkynyl‐Grignard Reagents S Murarka, A Studer Advanced Synthesis & Catalysis 353 (14‐15), 2708-2714, 2011 | 52 | 2011 |
Oxidative heterocycle formation using hypervalent iodine (III) reagents S Murarka, AP Antonchick Hypervalent Iodine Chemistry, 75-104, 2016 | 44 | 2016 |
Organophotoredox‐Catalyzed Cascade Radical Annulation of 2‐(Allyloxy)arylaldehydes with N‐(acyloxy)phthalimides: Towards Alkylated Chroman‐4‐one … S Das, SK Parida, T Mandal, L Sing, S De Sarkar, S Murarka Chemistry–An Asian Journal 15 (5), 568-572, 2020 | 42 | 2020 |
Direct C (sp3)–H activation of carboxylic acids A Uttry, M van Gemmeren Synthesis 52 (04), 479-488, 2020 | 42 | 2020 |
Radical/Anionic SRN1‐Type Polymerization for Preparation of Oligoarenes S Murarka, A Studer Angewandte Chemie International Edition 51 (49), 12362-12366, 2012 | 40 | 2012 |
Organophotoredox‐Catalyzed Late‐Stage Functionalization of Heterocycles S Kumar Hota, D Jinan, S Prakash Panda, R Pan, B Sahoo, S Murarka Asian Journal of Organic Chemistry 10 (8), 1848-1860, 2021 | 36 | 2021 |