| Colorimetric Sensing of Fluoride Ion by New Expanded Calix [4] pyrrole through Anion− π Interaction SP Mahanta, BS Kumar, S Baskaran, C Sivasankar, PK Panda Organic letters 14 (2), 548-551, 2012 | 81 | 2012 |
| Meso-diacylated calix [4] pyrrole: structural diversities and enhanced binding towards dihydrogenphosphate ion SP Mahanta, BS Kumar, PK Panda Chemical Communications 47 (15), 4496-4498, 2011 | 30 | 2011 |
| β,β′-Bipyrrole Fusion-Driven cis-Bimetallic Complexation in Isomeric Porphyrin BSKPKP Tridib Sarma Angewandte Chemie International Edition, 2015 | 28 | 2015 |
| Calix [4] pyrroles with shortest possible strap: Exclusively selective toward fluoride ion R Samanta, BS Kumar, PK Panda Organic letters 17 (17), 4140-4143, 2015 | 28 | 2015 |
| β-Hexaalkylporphycenes: positional effect of alkyl groups toward design and control of structural and photophysical properties in isomeric hexaethylporphycenes NN Pati, BS Kumar, PK Panda Organic letters 19 (1), 134-137, 2017 | 15 | 2017 |
| Hexaethylsubporphyrins: β-alkyl analogues in subporphyrin family ASPKP Brijesh Chandra, Sathish Kumar B, Navendu Mondal Dalton Transactions, 2015 | 14 | 2015 |
| 1D water chain stabilized by meso-expanded calix [4] pyrrole BS Kumar, PK Panda CrystEngComm 16 (37), 8669-8672, 2014 | 13 | 2014 |
| Meso-Free Boron(III)subchlorin and Its μ-Oxo Dimer with Interacting Chromophores B Chandra, R Soman, B Sathish Kumar, KVJ Jose, PK Panda Organic Letters 22 (24), 9735-9739, 2020 | 11 | 2020 |
| Synthetic access to calix[3]pyrroles via meso-expansion: hosts with diverse guest chemistry PKP B. Sathish Kumar, Narendra N. Pati, K. V. Jovan Jose Chemical Communications, 2020 | 10 | 2020 |
| New carbazole appended subporphyrin displaying intramolecular charge transfer and solid state fluorescence B Chandra, N Mondal, BS Kumar, PK Panda Journal of Porphyrins and Phthalocyanines 20 (01n04), 429-437, 2016 | 10 | 2016 |
| A2B- and A3-Type Boron(III)Subchlorins Derived from meso-Diethoxycarbonyltripyrrane: Synthesis and Photophysical Exploration R Soman, B Chandra, IA Bhat, BS Kumar, SS Hossain, S Nandy, ... The Journal of Organic Chemistry 86 (15), 10280-10287, 2021 | 9 | 2021 |
| Efficient synthesis of N-methyltetranitropyrrole: A stable, insensitive and high energy melt-castable material BSKPKP Vikranth Thaltiri, Kurumurthy Chavva New Journal of Chemistry 43, 12318-12324, 2019 | 9 | 2019 |
| β-Decamethoxysapphyrin and Its N-Benzyl Analogue A Rana, B Sathish Kumar, PK Panda Organic letters 17 (12), 3030-3033, 2015 | 9 | 2015 |
| Unsymmetrical bipyrrole derived highly soluble and emissive -dialkylporphycenes with good singlet oxygen generation ability NN Pati, B Satish Kumar, D Sivadasan, SS Sahoo, PK Panda Journal of Porphyrins and Phthalocyanines 24 (01n03), 121-128, 2020 | 8 | 2020 |
| Unsymmetrical Bipyrrole‐Derived β‐Tetraalkylporphycenes and C–H··· Br–C Interaction Induced 2D Arrays of the 2: 1 Supramolecular Sandwich Complex of Their cis‐/trans‐Dibromo … NN Pati, BS Kumar, B Chandra, PK Panda European Journal of Organic Chemistry 2017 (3), 741-745, 2017 | 8 | 2017 |
| 1, 2-Phenylene-Incorporated Smallest Expanded Calix [4] pyrrole via One-Step Synthesis of Tetrapyrrane: A Fluorescent Host for Fluoride Ion BS Kumar, B Chandra, KV Jovan Jose, PK Panda The Journal of Organic Chemistry 86 (15), 10536-10543, 2021 | 7 | 2021 |
| 3, 6, 13, 16-Tetrasubstituted Porphycene: The Missing Link in Porphycene Chemistry A Rana, B Sathish Kumar, PK Panda Organic Letters 22 (18), 7175-7180, 2020 | 6 | 2020 |
| Synthesis and anion binding properties of the smallest meso-expanded calix[4]pyrrole BS Kumar, PK Panda Journal of Chemical Sciences 130, 1-8, 2018 | 4 | 2018 |
| One-pot Synthesis of Benzotripyrrole Derivatives from 1H-pyrroles O Pandeeti, SB Kumar, P Panda New Journal of Chemistry, 2019 | 3 | 2019 |
| Meso expanded calix n pyrroles synthesis structural features and Meso expanded calix n pyrroles synthesis structural features and anion binding properties properties BS Kumar Hyderabad, 0 | | |
Dr. Pradeepta K PandaProfessor of ChemistryVerified email at uohyd.ac.in
