Samarium triflate-catalyzed halogen-promoted Friedel− crafts alkylation with alkenes S Hajra, B Maji, S Bar Organic Letters 9 (15), 2783-2786, 2007 | 70 | 2007 |
Stereoselective one-pot synthesis of oxazolines S Hajra, S Bar, D Sinha, B Maji The Journal of Organic Chemistry 73 (11), 4320-4322, 2008 | 64 | 2008 |
Design concept for α-hydrogen-substituted nitroxides AMS Michal Amar, Sukanta Bar, Mark A. Iron, Hila Toledo, Boris Tumanskii ... Nature Communications, 2015 | 41 | 2015 |
Catalytic enantioselective synthesis of A-86929, a dopamine D1 agonist S Hajra, S Bar Chemical communications 47 (13), 3981-3982, 2011 | 34 | 2011 |
Oxidative asymmetric umpolung alkylation of Evans’ β-ketoimides using dialkylzinc nucleophiles Tom A. Targel, Jayprakash N. Kumar, O. Svetlana Shneider, Sukanta Bar, Alex ... Organic & biomolecular chemistry 13 (9), 2546-2549, 2015 | 25 | 2015 |
A one-pot stereoselective synthesis of trans-1-aryl-2-aminotetralins from 2-arylethyl styrenes S Hajra, B Maji, D Sinha, S Bar Tetrahedron Letters 49 (25), 4057-4059, 2008 | 21 | 2008 |
Organocatalysis in the stereoselective bromohydrin reaction of alkenes S Bar Canadian Journal of Chemistry 88 (7), 605-612, 2010 | 20 | 2010 |
Lewis-base-catalyzed reductive aldol reaction to access quaternary carbons YC DePorre, JR Annand, S Bar, CS Schindler Organic letters 20 (9), 2580-2584, 2018 | 18 | 2018 |
Synthesis and stability of cyclic α-hydrogen nitroxides H Toledo, M Amar, S Bar, MA Iron, N Fridman, B Tumanskii, LJW Shimon, ... Organic & Biomolecular Chemistry 13 (43), 10726-10733, 2015 | 18 | 2015 |
Asymmetric synthesis of the dopamine D1 agonist, dihydrexidine S Hajra, S Bar Tetrahedron: Asymmetry 22 (7), 775-779, 2011 | 15 | 2011 |
Catalytic Aerobic Oxidation of Alcohols using Recoverable IAPNO α-Hydrogen Nitroxyl Radicals S Bar ChemCatChem, 2015 | 14 | 2015 |
Catalytic enantioselective synthesis of the dopamine D1 antagonist ecopipam S Hajra, S Bar Tetrahedron: Asymmetry 23 (2), 151-156, 2012 | 13 | 2012 |
Aluminum chloride-mediated dieckmann cyclization for the synthesis of cyclic 2-alkyl-1, 3-alkanediones: one-step synthesis of the chiloglottones AM Armaly, S Bar, CS Schindler Organic letters 19 (15), 3958-3961, 2017 | 11 | 2017 |
Acid chlorides as formal carbon dianion linchpin reagents in the aluminum chloride-mediated dieckmann cyclization of dicarboxylic acids AM Armaly, S Bar, CS Schindler Organic letters 19 (15), 3962-3965, 2017 | 9 | 2017 |
Asymmetric aminoarylation for the synthesis of trans-3-amino-4-aryltetrahydroquinolines: An access to aza-analogue of dihydrexidine SMS Akhtar, S Bar, S Hajra Tetrahedron 103, 132257, 2022 | 5 | 2022 |
Corrigendum to ‘‘Asymmetric synthesis of the dopamine D1 agonist, dihydrexidine’’[Tetrahedron: Asymmetry (2011) 775–779] S Hajra, S Bar Tetrahedron: Asymmetry 24 (5-6), 340, 2013 | 2 | 2013 |
Regioselective Synthesis of 5-Propyl-2-((trityloxy)methyl)thiophene-3-carbaldehyde S Bar Molbank, 2021 | 1 | 2021 |
Leveraging Baird aromaticity for advancement of bioimaging applications SCB Maxwell I. Martin, Avik K. Pati,Chathura S. Abeywickrama,Sukanta Bar ... Journal of physical organic chemistry, 2022 | | 2022 |
An efficient synthesis of substituted hexahydrobenzo[f]thieno[c]quinoline; an advanced intermediate of analog of A-86929, a dopamine D1 full agonist S Bar, MI Martin Canadian Journal of Chemistry 100 (8), 601-605, 2022 | | 2022 |
Regioselective Synthesis of 4-Bromo-3-formyl-N-phenyl-5-propylthiophene-2-carboxamide S Bar Molbank 4, M1296, 2021 | | 2021 |