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   Publications from IISER Thiruvananthapuram, India

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  1. Editorial: "λ3-Iodane-Mediated Umpolung of Ketone and Enolate to Enolonium".  Parida K. N. Cur. Org. Chem. 2024, DOI: 10.2174/0113852728302831240315064301.  (Bentham)

  2. “Chemistry of the Au-Thiol Interface through the Lens of Single Molecule Flicker Noise Measurements” Rashid, U.; Bro-Jørgensen, W.; Harilal, K. B.; Sreelakshmi P. A.; Mondal, R. R.; Varun C. P.; Solomon, G.; Parida K. N.;* Geetharani, K.;* Hammil, J. M.;* Kaliginedi, V.* J. Am. Chem. Soc. 2024, 146, 9063–9073. (ACS)

  3. "Dioxirane-Based Stereoselective and Oxidative Transformations" Neogi, I.;* Parida, K. N.* ChemistrySelect 2024, 9, e202400025. (Wiley)

  4. “Oxidation of Thiols with IBX or DMP: One-pot Access to Thiosulfonates or 2-Iodobenzoates and Applications in Functional Group Transformations” Chandra, A.;* Yadav, N. R.; Payra, S.; Parida, K. N.* Org. Lett., 2023, 25, 6256–6261. (ACS)

  5. “λ3- and λ5-Iodanes: Substituent Effects and Pseudorotation/Hypervalent Twisting” Parida, K. N.;* Moorthy, J. N.* Chem. Eur. J. 2023, 29, e202203997.  (Wiley, IF: 5.020)

  6. “Catalytic Oxidations with ortho-substituted Modified IBXs” Parida, K. N.;* Moorthy, J. N.* Synlett 2023, 34, 495–506. (Thieme, IF: 2.206)

  7. "Fluorinated Spacers: An Effective Strategy to Tailor Optoelectronic Properties and Stabilities of Metal-Halide Perovskites for Photovoltaic Applications" Mohanty, G.; Sebastian, A.; Haritha S, Parida, K. N.;* Neogi, I.* J. Mat. Chem. C 2022, 10, 16949–16982. (RSC, IF: 8.067)    

  8. “Dioxiranes: A Half-Century Journey” El-Assaad, T.; Zhu, J.; Sebastian, A.; McGrath, D. V.;* Neogi, I.;* Parida, K. N.* Org. Chem. Front. 2022, 9, 5675–5725. (RSC, IF: 5.456)

  9. “Construction and topological studies of a three-dimensional (3D) coordination polymer showing selective adsorption of aromatic hazardous dyes” Ahmed, A.; Ali, A.; Ahmed, M.; Parida, K.N; Ahmad, M.;* Ahmad, A.* Sep. Purif. Technol. 2021, 265, 118482. (Elsevier, IF: 9.136)

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  Publications from the University of Arizona, USA

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  1. “Beyond Simple Structure-Function Relationships: The Interplay of Geometry, Electronic Structure and Molecule/Electrode Coupling in Single-Molecule Junctions” Bamberger, N. D.; Dyer, D.; Parida, K. N.; El-Assaad, T.; Pursell, D.; McGrath, D. V.; Smeu, M.; Monti, O.* J. Phy. Chem. C 2022, 126, 6653–6661. (ACS, IF: 4.177)

  2. "Effect of Geometric Isomerism on Single Molecule Conductance in a Gold Mechanically-​Controlled Break Junction" El-Assaad, T.; Parida, K. N.; Bamberger, N.; Dyer, D.; Monti, O.; McGrath, D. V. ACS Meetings Spring 2022, CA, United States, DOI: 10.1021/scimeetings.2c00251.

  3. “Correlated Energy-Level Alignment Effects Determine Substituent-Tuned Single-Molecule Conductance” Ivie, J. A.; Bamberger, N. D.; Parida, K. N.; Shepard, S.; Dyer, D.; Saraiva-Souza, A.; Himmelhuber, R.; McGrath, D. V.;* Smeu, M.;* Monti, O* ACS Appl. Mater. Interfaces 2021,13, 4267–4277.  (ACS, IF: 10.38)

  4. “Grid-Based Correlation Analysis to Identify Rare Quantum Transport Behaviors” Bamberger, N. D.; Dyer, D.; Parida, K. N.; McGrath, D. V.; Monti, O.* J. Phy. Chem. C 2021, 125, 18297–18307. (ACS, IF: 4.177)

  5. “Sterically Driven Metal-Free Oxidation of 2,7-di-tert-butylpyrene” Al Assaad, T.; Parida, K. N.; Marcello, M.; McGrath, D. V.* Green Chem. 2020, 22, 5966–5971. (RSC, IF: 11.034)

  6. “Unsupervised Segmentation-Based as an Advanced Analysis Tool for Single-Molecule Break Junction Data” Bamberger, N; Ivie, J. A.; Parida, K. N.; McGrath, D. V.; Monti, O* J. Phy. Chem. C 2020, 124, 18302–18315.  (ACS, IF: 4.177)

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   Publications from Ariel University, Israel

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  1. A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species Arava, S.; Maksymenko, S.; Parida, K. N.; Pathe, G. K.; More, A. A.; Lipisa, Y. B.; Szpilman, A. M. J. Vis. Exp. 2018, e57916 (138), doi:10.3791/57916. (MyJoVE, IF: 1.4)

  2. "Cross-coupling of Dissimilar Ketone Enolates via Enolonium Species to Afford Non-symmetrical 1, 4-Diketones"Parida, K. N.; Pathe, G. K.; Maksymenko, S.; Szpilman, A. M. Beilstein J. Org. Chem. 2018, 14, 992–997. (Beilstein, IF: 2.54)

  3. "α-N-Heteroarylation and α-Azidation of Ketones via Enolonium Species" More,A. A.; Pathe, K. G.; Parida, K. N.; Maksymenko, S.; Lipisa, Y. B.; Szpilman, A. M. J. Org. Chem. 2018, 83, 2442–2447. (ACS, IF: 4.198)

  4. “Transition Metal-Free Intermolecular α-Arylation of Ketones via Enolonium Species” Maksymenko, S.; Parida, K. N.; Pathe, K. G.; More, A. A.; Lipisa,Y. B.; Szpilman, A. M. Org. Lett. 2017, 19, 6312–6315. (ACS, IF: 6.072)

  5. “Enolonium Species-Umpoled Enolates” Arava, S.; Kumar, J. N.; Maksymenko, S.; Iron, M. A.; Parida, K. N.; Fristrup, P.; Szpilman, A. M. Angew. Chem. Int. Ed. 2017, 56, 2599–2603. (Wiley, IF: 16.82)

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   Publications from IIT Kanpur, India​

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  1. “One-pot Synthesis of α-Bromo and α-Azido Ketone from Olefins using Catalytic Oxidation with in situ-Generated Modified IBX as a Key Reaction” Chandra, A.; Parida, K. N.; Moorthy, J. N. Tetrahedron 2017, 73, 5827–5832. (Elsevier, IF: 2.388)

  2. “Mixed Solvent Chemistry through Synergistic Solvation: Structure, Property and Function of t-BuOH-Dichloromethane Binary Solvent Mixtures” Gupta, S.; Parida, K. N.; Mukherjee, P.; Sen, P. J. Sol. Chem. 2017, 46, 461–675. (Springer, IF: 2.000)

  3. “Oxidation of Thiols to Sulphonic Acids with Oxone®/NaHCO3 and KBrO3” Parida, K. N.; Chandra, A.; Moorthy, J. N. ChemistrySelect 2016, 3, 490–494. Highlighted: ChemInform. (Wiley, IF: 2.307)

  4. “Synthesis of o-Carboxyarylacrylic Acids by Room Temperature Oxidative Cleavage of Hydroxy-naphthalenes and Higher Aromatics with Oxone®” Parida, K. N.; Moorthy, J. N. J. Org. Chem. 2015, 80, 8354–8360. Highlighted: ChemInform. (ACS, IF: 4.198)

  5. “Oxidative Cleavage of Olefins by In Situ Generated Catalytic 3,4,5,6-Tetramethyl-2-Iodoxybenzoic Acid/Oxone®” Moorthy, J. N.; Parida, K. N. J. Org. Chem. 2014, 79, 11431–11439. Highlighted: ChemInform, Organic Chemistry Portal. (ACS, IF: 4.198)

  6. “Oxidation Cascade with Oxone: Cleavage of Olefins to Carboxylic Acids” Parida, K. N.; Moorthy, J. N. Tetrahedron 2014, 70, 2280–2285. Highlighted: ChemInform. (Elsevier, IF: 2.388)

  7. “Through-Space Control of the Persistence of Photogenerated o-Quinonoid Intermediates in Naphthalenes Containing Cofacially Oriented Chromenes and Arenes” Moorthy, J. N.; Mandal, S.; Parida, K. N. Org. Lett. 2012, 14, 2438–2441. (ACS, IF: 6.072)

  8. “Oxidation of Benzyl Alcohols, Benzyl Halides, and Alkylbenzenes with Oxone” Parida, K. N.; Jhulki, S.; Mandal, S.; Moorthy, J. N. Tetrahedron 2012, 68, 9763–9768. Highlighted: ChemInform. (Elsevier, IF: 2.388)

  9. “Influence of (2,3,4,5,6-Pentamethyl/phenyl)phenyl Scaffold: Stereoelectronic Control of the Persistence of o-Quinonoid Reactive Intermediates of Photochromic Chromenes” Mandal, S.; Parida, K. N.; Samanta, S.; Moorthy, J. N. J. Org. Chem. 2011, 76, 7406–7414. (ACS, IF: 4.198)

  10. “Twist Does a Twist to the Reactivity: Stoichiometric and Catalytic Oxidations with Twisted Tetramethyl-IBX” Moorthy, J. N.; Senapati, K.; Parida, K. N.; Jhulki, S.; Sooraj, K.; Nair, N. N. J. Org. Chem. 2011, 76, 9593–9601. (ACS, IF: 4.198)

  11. “6-Membered Pseudocyclic IBX Acids: Syntheses, X-Ray Structural Characterizations, and Oxidation Reactivities in Common Organic Solvents” Moorthy, J. N.; Senapati, K.; Parida, K. N. J. Org. Chem. 2010, 75, 8416–8421. Highlighted: ChemInform (ACS, IF: 4.198)

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