pintu maity
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A Direct Synthesis of Selenophenes by Cu-Catalyzed One-Pot Addition of a Selenium Moiety to (E,E)-1,3-Dienyl Bromides and Subsequent Nucleophilic Cyclization
P Maity, D Kundu, R Roy, BC Ranu
Organic letters 16 (16), 4122-4125, 2014
Copper-Assisted Nickel Catalyzed Ligand-Free C(sp2)–O Cross-Coupling of Vinyl Halides and Phenols
D Kundu, P Maity, BC Ranu
Organic letters 16 (4), 1040-1043, 2014
Visible‐Light‐Photocatalyzed Metal‐Free C–H Heteroarylation of Heteroarenes at Room Temperature: A Sustainable Synthesis of Biheteroaryls
P Maity, D Kundu, BC Ranu
European Journal of Organic Chemistry 2015 (8), 1727-1734, 2015
Transition-Metal-Free Iodine Catalyzed Selenocayanation of Styrenyl Bromides and an Easy Access to Benzoselenophenes via Intermediacy of Styrenyl Selenocyanate
P Maity, B Paroi, BC Ranu
Organic letters 19 (21), 5748-5751, 2017
Cobalt-Catalyzed Remote C-4 Functionalization of 8-Aminoquinoline Amides with Ethers via C–H Activation under Visible-Light Irradiation. Access to α-Heteroarylated Ether …
T Ghosh, P Maity, BC Ranu
Organic letters 20 (4), 1011-1014, 2018
Cobalt‐Catalyzed Intermolecular C(sp2)O Cross‐Coupling
D Kundu, M Tripathy, P Maity, BC Ranu
Chemistry–A European Journal 21 (24), 8727-8732, 2015
Cobalt catalysed, copper assisted C (sp 2)–P cross coupling
T Ghosh, P Maity, D Kundu, BC Ranu
New Journal of Chemistry 40 (11), 9556-9564, 2016
Iron (0) nanoparticles mediated direct conversion of aryl/heteroaryl amines to chalcogenides via in situ diazotization
S Panja, P Maity, D Kundu, BC Ranu
Tetrahedron Letters 58 (35), 3441-3445, 2017
Access to Chiral GABA Analogues Bearing a Trifluoromethylated All-Carbon Quaternary Stereogenic Center through Water-Promoted Organocatalytic Michael Reactions
JH Sim, JH Park, P Maity, CE Song
Organic letters 21 (17), 6715-6719, 2019
Iodine‐Catalyzed Synthesis of Chalcogenophenes by the Reaction of 1, 3‐Dienyl Bromides and Potassium Selenocyanate/Potassium Sulfide (KSeCN/K2S)
P Maity, BC Ranu
Advanced Synthesis & Catalysis 359 (24), 4369-4378, 2017
Nickel–Copper‐Catalyzed C (sp2) N Cross‐Coupling of Cyclic and Bridged Amides: An Access to Cyclic Enamides and Alkenyl Vince Lactams
P Maity, D Kundu, BC Ranu
Advanced Synthesis & Catalysis 357 (16‐17), 3617-3626, 2015
Cu(OAc)2-Promoted Ortho C(sp2)–H Amidation of 8-Aminoquinoline Benzamide with Acyl Azide: Selective Formation of Aroyl or Acetyl Amide Based on Catalyst …
T Ghosh, P Maity, BC Ranu
The Journal of Organic Chemistry 83 (19), 11758-11767, 2018
Palladium-Catalyzed Ligand-Free Decarboxylative Coupling of α-Oxocarboxylic Acid with Aryl Diazonium Tetrafluoroborate: An Access to Unsymmetrical Diaryl Ketones
S Panja, P Maity, BC Ranu
The Journal of Organic Chemistry 83 (20), 12609-12618, 2018
Copper catalyzed cyanation through CC bond cleavage of gem-aryl dibromide followed by second cyanation of iodoarene by a released CN unit
P Maity, D Kundu, T Ghosh, BC Ranu
Organic Chemistry Frontiers 5 (10), 1586-1599, 2018
Calcium mediated C–F bond substitution in fluoroarenes towards C–chalcogen bond formation
P Maity, S Ahammed, RN Manna, BC Ranu
Organic Chemistry Frontiers 4 (1), 69-76, 2017
Visible light photocatalyzed carbon-heteroatom bond formation and synthesis of related compounds
N Mukherjee, P Maity, T Ghosh, S Panja, B C Ranu
Current Green Chemistry 3 (4), 279-317, 2016
Cobalt‐Copper Catalyzed C (sp2)–N Cross Coupling of Amides or Nitrogenated Heterocycles with Styrenyl or Aryl Halides
T Ghosh, P Maity, BC Ranu
ChemistrySelect 3 (16), 4406-4412, 2018
CFD modelling of a tubular reactor for methanol synthesis
T Bhatelia, J Patel, R Pranab, P Maity, RK Voolapalli, PA Webley
Asia Pacific Confederation of Chemical Engineering Congress, 2015
Synthesis of Bioactive Five-and Six-Membered Heterocycles Catalyzed by Heterogeneous Supported Metals
BC Ranu, T Chatterjee, N Mukherjee, P Maity, B Majhi
Green Synthetic Approaches for Biologically Relevant Heterocycles, 7-43, 2015
Recent Developments in FCC Process and Catalysts
AR Khande, PK Dasila, S Majumder, P Maity, C Thota
Catalysis for Clean Energy and Environmental Sustainability, 65-108, 2021
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