Sanjay Batra
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Advances in the Baylis-Hillman reaction-assisted synthesis of cyclic frameworks
V Singh, S Batra
Tetrahedron 64, 4511-4574, 2008
Advances in the syntheses of quinoline and quinoline-annulated ring systems
S Madapa, Z Tusi, S Batra
Current Organic Chemistry 12 (13), 1116-1183, 2008
Applications of allylamines for the syntheses of aza-heterocycles §
S Nag, S Batra
In search of new chemical entities with spermicidal and anti-HIV activities
S Srivastava, LK Bajpai, S Batra, AP Bhaduri, JP Maikhuri, G Gupta, ...
Bioorganic & medicinal chemistry 7 (11), 2607-2613, 1999
Search for new pharmacophores for antimalarial activity. Part II: Synthesis and antimalarial activity of new 6-ureido-4-anilinoquinazolines
S Madapa, Z Tusi, A Mishra, K Srivastava, SK Pandey, R Tripathi, SK Puri, ...
Bioorganic & medicinal chemistry 17 (1), 222-234, 2009
Immunological and toxicological risk assessment of e-cigarettes
G Kaur, R Pinkston, B Mclemore, WC Dorsey, S Batra
European Respiratory Review 27 (147), 2018
Synthesis of β-Carboline-Based N-Heterocyclic Carbenes and Their Antiproliferative and Antimetastatic Activities against Human Breast Cancer Cells
SU Dighe, S Khan, I Soni, P Jain, S Shukla, R Yadav, P Sen, SM Meeran, ...
Journal of Medicinal Chemistry 58 (8), 3485-3499, 2015
Deletion of Nlrp3 augments survival during polymicrobial sepsis by decreasing autophagy and enhancing phagocytosis
L Jin, S Batra, S Jeyaseelan
The Journal of Immunology 198 (3), 1253-1262, 2017
Structure-based approach to falcipain-2 inhibitors: synthesis and biological evaluation of 1, 6, 7-trisubstituted dihydroisoquinolines and isoquinolines
S Batra, YA Sabnis, PJ Rosenthal, MA Avery
Bioorganic & medicinal chemistry 11 (10), 2293-2299, 2003
Simple and efficient synthesis of substituted 2-pyrrolidinones, 2-pyrrolones, and pyrrolidines from enaminones of Baylis− Hillman derivatives of 3-isoxazolecarbaldehydes
V Singh, R Saxena, S Batra
The Journal of Organic Chemistry 70 (1), 353-356, 2005
Iodine-Mediated Intramolecular Electrophilic Aromatic Cyclization in Allylamines: A General Route to Synthesis of Quinolines, Pyrazolo [4, 3-b] pyridines, and Thieno [3, 2-b …
H Batchu, S Bhattacharyya, S Batra
Organic letters 14 (24), 6330-6333, 2012
Applications of morita-baylis-hillman reaction to the synthesis of natural products and drug molecules
S Bhowmik, S Batra
Current Organic Chemistry 18 (24), 3078-3119, 2014
Open source drug discovery: highly potent antimalarial compounds derived from the tres cantos arylpyrroles
AE Williamson, PM Ylioja, MN Robertson, Y Antonova-Koch, V Avery, ...
ACS central science 2 (10), 687-701, 2016
Search for new pharmacophores for antimalarial activity. Part I: synthesis and antimalarial activity of new 2-methyl-6-ureido-4-quinolinamides
S Madapa, Z Tusi, D Sridhar, A Kumar, MI Siddiqi, K Srivastava, A Rizvi, ...
Bioorganic & medicinal chemistry 17 (1), 203-221, 2009
A systematic review of smoking-related epigenetic alterations
G Kaur, R Begum, S Thota, S Batra
Archives of Toxicology 93, 2715-2740, 2019
Trifluoroacetic acid: a more effective and efficient reagent for the synthesis of 3-arylmethylene-3,4-dihydro-1H-quinolin-2-ones and 3-arylmethyl-2-amino-quinolines …
R Pathak, S Madapa, S Batra
Tetrahedron 63 (2), 451-460, 2007
Iron nitrate/TEMPO: a superior homogeneous catalyst for oxidation of primary alcohols to nitriles in air
SU Dighe, D Chowdhury, S Batra
Advanced Synthesis & Catalysis 356 (18), 3892-3896, 2014
Combinatorial synthesis and biological evaluation of isoxazole-based libraries as antithrombotic agents
S Batra, T Srinivasan, SK Rastogi, B Kundu, A Patra, AP Bhaduri, M Dixit
Bioorganic & medicinal chemistry letters 12 (15), 1905-1908, 2002
Synthesis and antibacterial evaluation of ureides of Baylis–Hillman derivatives
S Nag, R Pathak, M Kumar, PK Shukla, S Batra
Bioorganic & medicinal chemistry letters 16 (14), 3824-3828, 2006
Synthesis of 3,4,5‐Trisubstituted Isoxazoles from Morita–Baylis–Hillman Acetates by an NaNO2/I2‐Mediated Domino Reaction
SU Dighe, S Mukhopadhyay, S Kolle, S Kanojiya, S Batra
Angewandte Chemie 127 (37), 11076-11080, 2015
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