VOSO4 catalyzed highly efficient synthesis of benzimidazoles, benzothiazoles, and quinoxalines CS Digwal, U Yadav, AP Sakla, PVS Ramya, S Aaghaz, A Kamal Tetrahedron Letters 57 (36), 4012-4016, 2016 | 74 | 2016 |
Exploration of carbamide derived pyrimidine-thioindole conjugates as potential VEGFR-2 inhibitors with anti-angiogenesis effect S Sana, VG Reddy, S Bhandari, TS Reddy, R Tokala, AP Sakla, ... European Journal of Medicinal Chemistry 200, 112457, 2020 | 65 | 2020 |
An insight into medicinal attributes of dithiocarbamates: Bird’s eye view SD Shinde, AP Sakla, N Shankaraiah Bioorganic Chemistry 105, 104346, 2020 | 64 | 2020 |
Structural insights of oxindole based kinase inhibitors as anticancer agents: Recent advances P Dhokne, AP Sakla, N Shankaraiah European journal of medicinal chemistry 216, 113334, 2021 | 62 | 2021 |
Syntheses and applications of spirocyclopropyl oxindoles: a decade review AP Sakla, P Kansal, N Shankaraiah European Journal of Organic Chemistry 2021 (5), 757-772, 2021 | 50 | 2021 |
An update on the progress of cycloaddition reactions of 3-methyleneindolinones in the past decade: versatile approaches to spirooxindoles R Saeed, AP Sakla, N Shankaraiah Organic & Biomolecular Chemistry 19 (36), 7768-7791, 2021 | 35 | 2021 |
Syntheses and reactivity of spiro-epoxy/aziridine oxindole cores: developments in the past decade AP Sakla, P Kansal, N Shankaraiah Organic & Biomolecular Chemistry 18 (42), 8572-8596, 2020 | 35 | 2020 |
Reliability of click chemistry on drug discovery: A personal account N Shankaraiah, AP Sakla, K Laxmikeshav, R Tokala The Chemical Record 20 (4), 253-272, 2020 | 33 | 2020 |
TCCA-mediated oxidative rearrangement of tetrahydro-β-carbolines: facile access to spirooxindoles and the total synthesis of (±)-coerulescine and (±)-horsfiline M Sathish, AP Sakla, FM Nachtigall, LS Santos, N Shankaraiah RSC advances 11 (27), 16537-16546, 2021 | 14 | 2021 |
FeCl3‐Catalyzed [3+2] Cycloaddition Reaction: A Mild Synthetic Approach to Spirooxindolo‐2‐iminothiazolidine Scaffolds S Bhandari, AP Sakla, N Shankaraiah ChemistrySelect 5 (10), 2886-2891, 2020 | 12 | 2020 |
Design and synthesis of 5‐Morpholino‐Thiophene‐Indole/Oxindole hybrids as cytotoxic agents U Yadav, AP Sakla, R Tokala, ST Nyalam, A Khurana, CS Digwal, V Talla, ... ChemistrySelect 5 (14), 4356-4363, 2020 | 11 | 2020 |
One-pot, microwave-assisted copper (I)-catalysed dithiocarbamation: facile introduction of dithiocarbamate on imidazopyridines K Laxmikeshav, AP Sakla, SE John, N Shankaraiah Green Chemistry 24 (3), 1259-1269, 2022 | 10 | 2022 |
Dithiocarbamation of spiro-aziridine oxindoles: A facile access to C3-functionalised 3-thiooxindoles as apoptosis inducing agents AP Sakla, B Panda, K Laxmikeshav, JP Soni, S Bhandari, C Godugu, ... Organic & Biomolecular Chemistry 19 (48), 10622-10634, 2021 | 10 | 2021 |
Lewis-acid catalyzed dehydrative [3+ 2] cycloaddition reaction: A facile synthetic approach to spiro-benzoindoline oxindoles S Bhandari, N Kulkarni, AP Sakla, N Shankaraiah Tetrahedron Letters 61 (25), 152007, 2020 | 10 | 2020 |
Microwave‐Assisted Regioselective Friedel–Crafts Arylation by BF3 ⋅ OEt2: A Facile Synthetic Access to 3‐Substituted‐3‐Propargyl Oxindole Scaffolds K Laxmikeshav, AP Sakla, S Rasane, SE John, N Shankaraiah ChemistrySelect 5 (23), 7004-7012, 2020 | 9 | 2020 |
Regioselective synthesis and in vitro cytotoxicity evaluation of 3-thiooxindole derivatives: Tubulin polymerization inhibition and apoptosis inducing studies AP Sakla, B Panda, A Mahale, P Sharma, K Laxmikeshav, MA Khan, ... Bioorganic & Medicinal Chemistry 90, 117297, 2023 | 2 | 2023 |
Development of Benzimidazole‐Substituted Spirocyclopropyl Oxindole Derivatives as Cytotoxic Agents: Tubulin Polymerization Inhibition and Apoptosis Inducing Studies AP Sakla, MR Bazaz, A Mahale, P Sharma, DG Valapil, OP Kulkarni, ... ChemMedChem, e202400052, 2024 | | 2024 |
A validated high‐performance liquid chromatography method for the determination of brassinin, an indoleamine 2, 3‐dioxygenase inhibitor in rat plasma P Dhurjad, K Gupta, AP Sakla, N Shankaraiah, R Sonti Separation Science Plus 6 (11), 2300073, 2023 | | 2023 |