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Akash Sakla
Akash Sakla
National Institute of Pharmaceutical Education and Research (NIPER) Ahmedabad, India
Verified email at niperahm.res.in
Title
Cited by
Cited by
Year
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
732016
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
672020
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
612021
An insight into medicinal attributes of dithiocarbamates: Bird’s eye view
SD Shinde, AP Sakla, N Shankaraiah
Bioorganic Chemistry 105, 104346, 2020
612020
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
492021
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
342021
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
342020
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
272020
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
132021
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
122020
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
112020
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
102022
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
102021
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
102020
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
92020
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
12023
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
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