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Akash Sakla
Akash Sakla
National Institute of Pharmaceutical Education and Research (NIPER) Ahmedabad, India
在 niperahm.res.in 的电子邮件经过验证
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引用次数
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年份
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
742016
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
652020
An insight into medicinal attributes of dithiocarbamates: Bird’s eye view
SD Shinde, AP Sakla, N Shankaraiah
Bioorganic Chemistry 105, 104346, 2020
642020
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
622021
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
502021
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
352021
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
352020
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
332020
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
142021
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
22023
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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