76. Difluoromethylation of N-heterocyclic biomolecules

S. Kumawat, C. Dewangan, K. L. M. N. S. Jyothi, K. Sadhana, K. Natte* : J. Fluor. Chem. 2025, 288, 110499 

75. N-Selective Difluoromethylation of 4-Hydroxyquinolines

S. Kumawat, G. N. Nair, V. N. Kalevaru, S. Wohlrab, T. Tarasiuk, T. Yegorova, P. K. Mykhailiuk*, K. Natte* : Org. Lett. 2025, 27, 41, 11466–11473 

 74. Advances in trifluoromethylation of C(sp3)-H bonds

  S. Kumawat, T. Bhatt, V. Goyal, H. Neumann, R. Zbořil, R. V. Jagadeesh*, M. Beller*, K. Natte* : Coord. Chem. Rev. 2025, 542, 216885

 73. CO2 Valorization toward Selective N-Formylation of Nitroarenes and Aminoarenes under Homogeneous Titanium Catalysis

V. Suman ‡, T. Bhatt ‡, G. N. Nair, V. N. Kalevaru*, S. Wohlrab*, K. Natte*: ACS Sustainable Chem. Eng. 2025,  https://doi.org/10.1021/acssuschemeng.5c06978

72. A biomass-derived nickel-based nanomaterial as a sustainable and reusable catalyst for hydrogenation of arenes and heteroarenes

V. Goyal, T. Bhatt, A. Kuttasseri, A. Mahata*, R. Zbořil*, K. Natte*, R. V. Jagadeesh* : RSC Sustainability, 2025, 3, 2235-2245 

71. Chemoselective transfer hydrogenation and transfer deuteration of substituted quinolines using Hantzsch ester and D2O

T. Bhatt , T. Dutta , K. Yaswanth, V. N. Kalevaru, S. Wohlrab,  K, Natte* : Chem. Commun., 2025, 61, 12305-12308 

70. DAST Enabled Synthesis of Fluorinated Amides and Fatty Acid Amides Including Drugs under Ambient Conditions

S. Kumawat, K. L. M. N. S. Jyothi, V. N. Kalevaru, S. Wohlrab*, K. Natte*: Org. Lett. 2025, 27, 32, 8829–8834

69. Dearomative Difluoromethylation of N-Heterocycles and Pharmaceuticals with Bromo(difluoro)acetic Acid

S. Kumawat, T. Bhatt, K. Natte*: J. Org. Chem. 2025, 90, 28, 9826–9844 

68. Nickel‐Catalyzed Synthesis of Structurally Diverse N‐(hetero) aryl Pyrroles 

Chitrarekha Dewangan, Swapnaneel Sarmah, K. Natte*: Asian J. Org. Chem. 2025, 14, DOI: 10.1002/ajoc.202500195 

67. Silver (I) Oxide Catalyzed C/S–H Trifluoromethylation of Arenes and Heteroarenes with Sodium Trifluoromethanesulfinate

K. Sadhana ‡,  S. Kumawat ‡, K. L. M. N. S Jyothi, K. Natte*: Synlett  2025, 36(15) 2261-2266 

66. Dearomative selective reduction of structurally diverse N-heteroarenes enabled by a homogeneous titanium catalyst

T. Bhatt , V. Suman , M. Choudhary, S. K. Singh b, K. Natte*: J. catal. 2025, 443, 115937

65. Accessing Structurally Diverse Aryl Difluoromethyl Ethers with Bromo(difluoro)acetic Acid 

S. Kumawat, K. Natte*: Chem. Comm. 2024, 60, 13935-13938 

64. Practical and scalable hydrogenation of nitro compounds using palladium-based nanocatalyst under ambient conditions

V. Vakati a, V. Goyal a b, A. S. Alshammari c, N. V. Kalevaru a, S. Wohlrab a, K. Natte d, R. Zbořil b e, R. V. Jagadeesh a b: Catal. Today, 2024, 442, 114940

63. Ammonia-Borane Dependent Transfer Hydrogenation of Carboxylic Esters to Primary Alcohols

S. Kumawat, S. Dey, K. Natte*: J. Org. Chem. 2024, 89, 15, 10719–10728 

62. Iron(II) triflate as a Photocatalyst for Trifluoromethylation of Functionalized Arenes under Blue LED Light: Access to Bioactive Compounds 

S. Kumawat, K. Natte*: J. Catal., 2024, 434, 15506 

61. Valorization of Bio-Renewable Glycerol by Catalytic Amination Reactions

S. Kumawat, S. Singh, T. Bhatt, T. Maurya, S. Vaidyanathan, K. Natte,* J. Rajenahally: Green Chem., 2024, 26, 3021-3038 

60. Transfer Hydrogenation of N- and O-containing heterocycles Including Pyridines with H3N–BH3 Under the Catalysis of the Homogeneous Ruthenium Precatalyst

T. Bhatt, K. Natte,* : Org. Lett. 2024, 26, 4, 866–871 [Highlighted in "OPR&D" Org. Process Res. Dev. 2024, 28, 3, 641–651 and Organic Chemistry portal] 

59. Selective hydrogenation of carbonyl compounds and olefins using an efficient combination of homogeneous RuCl3/1,10-Phenanthroline

N. Sarki, S. Kumawat, M. Choudhary, A. Narani, S. K. Singh, K. Natte,* : J. Catal. 2023, 429, 115248 

58. Homogenous Nickel-Catalyzed Chemoselective Transfer Hydrogenation of Functionalized Nitroarenes with Ammonia-Borane

C. Dewangan, S. Kumawat, T. Bhatt, K. Natte,*: Chem. Commun. 2023, 59, 14709-14712 

57. Earth-Abundant Heterogeneous Cobalt Catalyst for Selective Ring Hydrogenation of (Hetero)arenes and Gram Scale Synthesis of Pharmaceutical Intermediates.

B. Singh, V. Goyal, D. Sarma, R. Kumar, T. Bhatt, A. Mahata, C. R. Reddy, A. Narani, K. Natte,*: ACS Catal., 2023,13, 9724–9744 [Highlighted in 'Synfacts' 2023; 19(10): 1016] 

56. General and selective homogeneous Ru-catalyzed transfer hydrogenation, deuteration, and methylation of functional compounds using methanol.

M. Subaramanian, G. Sivakumar, V. G. Landge, R. Kumar, K. Natte, R. V. Jagadeesh, E. Balaraman: J. Catal., 2023, 425, 386-405 

55. Methanol as a Potential Hydrogen Source for Reduction Reactions Enabled by a Commercial Pt/C Catalyst.

V. Goyal,T. Bhatt, C. Dewangan, A. Narani, G. Naik, E. Balaraman, K. Natte* and Rajenahally V. Jagadeesh: J. Org. Chem. 2023, 88, 2245−2259 

54.  Challenges and Recent Advancements in the Transformation of CO2 to Carboxylic acids: Straightforward Assembly with homogeneous 3d Metals. 

R. Cauwenbergh, V. Goyal, R. Maiti, K. Natte,* S. Das: Chem. Soc. Rev., 2022, 51, 9371-9423

53. Recent Advances in the Catalytic N-Methylation and N-Trideuteromethylation Reactions Using Methanol and Deuterated Methanol.

 V. Goyal, N. Sarki, A. Narani, G. Naik, K. Natte,* R. V. Jagadeesh: Coordination Chemistry Reviews, 2022, 474, 214827

52. Cu-Oxide Nanoparticles Catalyzed Synthesis of Nitriles and Amides from Alcohols and Ammonia in Presence of Air.

T. Senthamarai, F. Poovan, A. M. Alenad, N. Rockstroh, J. Rabeah, S. Bartling, E. Baráth, K. Natte,* R. V Jagadeesh: Adv. Sustainable Syst.2022, 6, 2200263

50. Synergy between homogeneous and heterogeneous catalysis.

F. Poovan, V. Chandrashekhar, K. Natte,* J. Rajenahally*: Catal. Sci. Technol., 2022, doi.org/10.1039/D2CY00232A

49. Recent Trends in Upgrading of CO2 as a C1 Reactant in N- and C-Methylation Reactions

G. Naik, N. Sarki, V. Goyal, A. Narani, K. Natte*: Asian J. Org. Chem., 2022, doi.org/10.1002/ajoc.202200270

48. Value addition of Lignin to Zingerone using recyclable AlPO4 and Ni/LRC Catalysts

S. Rawat, B. Singh, B. Raju, C. Pendem, S. Bhandari, K. Natte,* A. Narani: Chem. Eng. J, 2022, 431, 13413

47. Reductive Amination, Hydrogenation and hydrodeoxygenation of 5-Hydroxymethylfurfural using Silica-supported Cobalt-Nanoparticles.

Vishwas G. Chandrashekhar, Dr. Kishore Natte, Dr. Asma M. Alenad, Dr. Ahmad S. Alshammari, Dr. Carsten Kreyenschulte, Prof. Dr. Rajenahally V. Jagadeesh: ChemCatChem, 2021,14, 01234

46. Base metal‐catalyzed C‐methylation reactions using methanol.

N. Sarki, V. Goyal, K. Natte,* R. V. Jagadeesh*: Adv. Synth. Catal, 2021, 22, 5028-5046 

45.  Recent developments in reductive N-methylation with base-metal catalysts. 

V. Goyal, G. Naik, A. Narani, K. Natte,* R. V. Jagadeesh: Tetrahedron, 2021, 98, 132414

44.  Biorenewable carbon-supported Ru catalyst for N-Alkylation of Amines with Alcohols and Selective Hydrogenation of Nitroarenes.

V. Goyal, N. Sarki, M. K. Poddar, A. Narani, D. Tripathi, A. Ray, K. Natte*: New J. Chem., 2021, 45, 14687-14694

43.  Pd/C-catalyzed transfer hydrogenation of aromatic nitro compounds using methanol as a hydrogen source.

V. Goyal, N. Sarki, K. Natte*, A. Ray: J. Indian Chem. Soc., 2021, 98,100014

42. Simple RuCl3-catalyzed N-Methylation of Amines and Transfer Hydrogenation of Nitroarenes using Methanol.

N. Sarki, V. Goyal, N. K. Tyagi, Puttaswamy, A. Narani, A. Ray, K. Natte*: ChemCatChem, 2021, 7, 1722-1729 (Very Important Manuscript)

41. Carbon-Supported Cobalt Nanoparticles as Catalysts for the Selective Hydrogenation of Nitroarenes to Arylamines and Pharmaceuticals.

V. Goyal, N. Sarki, B. Singh, A. Ray, M. Poddar, A. Bordoloi, A. Narani, K. Natte*: ACS Appl. Nano Mater, 2020, 11, 11070-11079

40. Biocarbon supported ruthenium-oxide based catalyst for hydrogenation of arenes and heteroarenes.

 A. Kumar, V. Goyal, N. Sarki, B. Singh, A. Ray, T. Bhaskar, A. Bordoloi, A. Narani, K. Natte*: ACS Sustainable Chem. Eng., 2020, 41, 15740-15754

39. Synthesis of Functional Chemicals from Lignin‐derived Monomers by Selective Organic Transformations.

        K. Natte*, A. Narani, V. Goyal, N. Sarki, R. V Jagadeesh*, Adv. Synth. Catal, 2020, 23, 5143-5169

38.  Pd-Nanoparticles immobilized organo-functionalized SBA-15: An efficient heterogeneous catalyst for selective hydrogenation of C-C double bonds of α, β-unsaturated carbonyl compounds

     A. Narani, H.P.R. Kannapu, K. Natte, D. R Burri: Mol. Catal ,2020, 497,111200

37. Molybdenum-catalyzed oxidative depolymerization of alkali lignin: Selective production of Vanillin

        S. Rawat, P. Gupta, B. Singh, T. Bhaskar, K. Natte*, A. Narani, Appl. Catal. A-Gen, 2020, 598, 117567

36. Catalytic reductive aminations using molecular hydrogen for synthesis of different kinds of amines

        K.Murugesan, T.Senthamarai, V.Chandrashekhar, K.Natte, P.Kamer, M.Beller, J.Rajenahally: Chem. Soc. Rev. , 2020, 49, 6273-6328

35. Scalable preparation of stable and reusable silica supported palladium nanoparticles as catalysts for N-alkylation of amines with alcohols

        A. S Alshammari, K. Natte, N. V. Kalevaru, A. Bagabas, R. V Jagadeesh: J. Catal. , 2020, 382, 141-149

34. Commercial Pd/C-Catalyzed N-Methylation of Nitroarenes and Amines Using Methanol as Both C1 and H2 Source

        V. Goyal, J. Gahtori, A. Narani, P. Gupta, A. Bordoloi, K. Natte*: J. Org. Chem, 2019, 23, 15389-15398

33. Expedient Synthesis of N-Methyl- and N-Alkylamines by Reductive Amination using Reusable Cobalt Oxide Nanoparticle.

        T.Senthamarai, K.Murugesan, K.Natte, N.Kalevaru, H.Neumann, P.Kamer , J.Rajenahally: ChemCatChem, 2018, 10,1235-1240

32. Catalytic Utilization of Methanol as a C1 Source in Chemical Synthesis

        K.Natte, H.Neumann, M.Beller, R.V.Jagadeesh: Angew Chem. Int. Ed. , 2017, 56, 6384-6394

31. Convenient Reductive Aminations without Hydrogen: Selective Iron-catalyzed Synthesis of N-Methylamines

         K.Natte, R.V.Jagadeesh, H.Neumann, M.Beller: Nat. Commun, 2017,1344-1353

30. Synthesis of Nitriles from Amines using Nanoscale Co3O4-based Catalysts via Sustainable Aerobic Oxidation

        K.Natte, R.V.Jagadeesh, M.Sharif, H.Neumann, M. Beller: Org. Biomol. Chem. , 2016, 14,3356-3359

29. Palladium Catalyzed Trifluoromethylation of Hetero(arenes) with CF3Br

        K.Natte, R.V.Jagadeesh, L.He, J.Rabeah, C.Taeschler, H.Neumann, A.Brückner ,   

        M.Beller: Angew Chem. Int. Ed. , 2016,  55, 272-2786

28. Palladium-catalyzed Carbonylative C–H Activation of Arenes with Norbornene as the     Coupling Partner

        J.Chen, K.Natte, X - F.Wu: J. Organomet. Chem. , 2016, 803, 9-12

27. The Applications of Dimethyl Sulfoxide as Reagent in Organic Synthesis

        X - F.Wu, K.Natte: Adv. Synth. Catal , 2016, 358,336-352

26. Heterogeneous Pt-Catalyzed C-H Perfluoroalkylation of Arenes and Heteroarenes

        L.He, K.Natte, J.Rabeah, C.Taeschler, H.Neumann, A.Brückner, M.Beller: Angew. Chem. Int. Ed. , 2015, 54, 4320-4324

25. Nitrogen-Doped Graphene Activated Iron Oxide-based Nanocatalysts for Selective Transfer Hydrogenation of Nitroarenes

       R.V.Jagadeesh, K.Natte, H.Junge, M.Beller: ACS Catal , 2015, 5, 1526-1529

24. Pd/C as an Efficient Heterogeneous Catalyst for Carbonylative Four- Component Synthesis of 4(3H)-Quinazolinones

        K. Natte, H. Neumann, X.-F. Wu: Catal. Sci. Technol, 2015, 4474-4480

23. Palladium-Catalyzed Carbonylative Cyclization of Arenes via C-H Bond Activation with DMF as the Carbonyl Source.

        J. Chen, J. Feng, K. Natte, X.-F. Wu: Chem. Eur. J. , 2015, 21,16370-16373.

22. Pd/C-catalyzed carbonylative C–H activation with DMF as the CO source

         J. Chen, K. Natte, X.-F. Wu: Tetrahedron Lett, 2015, 56, 6413-6416

21. Iron-catalyzed reduction of aromatic aldehydes with paraformaldehyde and H2O as the hydrogen source

        K. Natte, W. Li, S. Zhou, H. Neumann, X-F. Wu: Tetrahedron Lett, 2015, 56, 1118-11121

20. Convenient copper-mediated Chan–Lam coupling of 2-aminopyridine: facile synthesis of N-arylpyridin-2-amines

        J. Chen, K. Natte, N. Y. T Man, S. G Stewart, X-F. Wu: Tetrahedron Lett, 2015, 56,4843-4847

19. Convenient Palladium-Catalyzed Carbonylative Synthesis of Caprolactam and Butyrolactam Derived Phthalimides and Amides by using DBU and DBN as the Nitrogen Source

        J. Chen, K. Natte, H. Neumann, Xiao-Feng Wu: Tetrahedron Lett , 2015, 56,342-345

18. Palladium-Catalyzed Carbonylations of Aryl Bromides by using Paraformaldehyde: Synthesis of aldehydes and esters

        K. Natte, A. Dumrath, H. Neumann, M. Beller: Angew. Chem. Int. Ed, 2014, 53, 10090-10094

17. Base-Controlled Selectivity toward Linear and Angular Fused Quinazolinone Cores via Palladium-Catalyzed Carbonylation/Nucleophilic Aromatic Substitution Sequence

        J. Chen, K. Natte, A. Spannenberg, H. Neumann, P.Langer, M. Beller, X.-F. Wu: Angew. Chem. Int. Ed. , 2014, 53, 7579-7583

16. Palladium-Catalyzed Oxidative Carbonylative Coupling of Arylboronic acids with Terminal Alkynes to Alkynones

        K. Natte, J. Chen, H. Neumann, M. Beller, X.-F. Wu: Org. Biomol. Chem. , 2014, 12, 5590-5593

15. Palladium-Catalyzed Carbonylation of 2- Bromoanilines with 2-Formylbenzoic acid and 2-halobenzaldehydes: Efficient Synthesis of Functionalized Isoindolinones

        K. Natte, J. Chen, H. Li, H. Neumann, M. Beller, X.-F. Wu: Chem. Eur. J. , 2014, 20, 14184-14188

14. Efficient Palladium-Catalyzed Double Carbonylation of o-Dibromobenzenes: Synthesis of Thalidomide

        J. Chen*, K. Natte*, A. Spannenberg, H. Neumann, M. Beller, X.-F. Wu: Org. Biomol. Chem. , 2014,12, 5578-5581

13. Palladium-Catalyzed Carbonylative [3+2+1] Annulation of N-Aryl-pyridine-2-amines with Internal Alkynes via C-H Activation: Facile Synthesis of 2-Quinolinones

       J. Chen, K. Natte, H. Neumann, M. Beller, X.-F. Wu: Chem. Eur. J. , 2014, 20, 14189-14193

12.  Palladium@Cerium(IV) oxide-Catalyzed Oxidative Synthesis of N-(2-Pyridyl)Indoles via C-H Activation Reaction

        J. Chen, L. He, K. Natte, H. Neumann, M. Beller, X.-F. Wu: Adv. Synth. Catal, 2014, 356, 2955-2959

11. Palladium-Catalyzed Carbonylative Reactions of 1-Bromo-2-fluorobenzenes with Various Nucleophiles: Effective Combination of Carbonylation and Nucleophilic Substitution

       J. Chen, K. Natte, H. Neumann, X.-F. Wu: Chem. Eur. J. , 2014, 20, 16107-16110

10. A Convenient Palladium-Catalyzed Carbonylative Synthesis of Quinazolines from 2-Aminobenzylamine and Aryl Bromides

      J. Chen, K. Natte, H. Neumann, M. Beller, X.-F. Wu: RSC Adv. , 2014, 4, 56502-56505

9. Morphological and elemental analysis of single engineered nanoparticles by high-resolution imaging with SEM/T-SEM, EDX and SAM

      S. Rades, V-D. Hodoroaba, T. Wirth, M. P. Lobera, R. H. Labrador, K. Natte, T. Behnke, T. Grossa, W. E. S. Unger: RSC Adv, 2014, 4, 49577-49587

8. Impact of polymer shell on the formation and time evolution of nanoparticle-protein corona

      K. Natte, J. Friedrich, S. Wohlrab, J. Lutzki, R. von Klitzing, W. Österle, G. Orts-Gil: Colloids Surf. B, 2013, 104, 213-220

7. On the role of protein corona formation and evolution in the colloidal stability of nanoparticles

      G. Orts-Gil, K. Natte, R.Thiermann, M.Girod, A.Thünemann, M.Maskos, W. Österle: Colloids Surf. B. , 2013, 108, 110-119

6. Multi-parametric reference nanomaterials for toxicology: state of the art, future challenges and potential candidates

      G. Orts-Gil, K. Natte, W. Österle: RSC Adv. , 2013, 3, 18202-18215

5. Morphology of Nanoparticles- A Characterization using High-Resolution SEM.

V. Hodoroaba, S. Rades, K. Natte, G. Orts-Gil, W. S. Unger: Imaging and Microscopy, 2013, 13, 54-56

4. Tuning interfacial properties and colloidal behavior of hybrid nanoparticles by controlling the polymer precursor

      K. Natte, G. Orts-Gil, J. Friedrich, R. von Klitzing, W. Österle, Macromol: Chem. Phys. , 2012, 231, 2412-2419

3. Synthesis and characterization of highly fluorescent core-shell nanoparticles based on Alexa-Dyes

      K. Natte, T.Bhenke, G. Orts-Gil, C.Würth, U.R.Genger, J. Friedrich, W. Österle: J. Nanopart. Res. , 2012,  14, 680-670

2. Characterization of silica nanoparticles prior to in vitro studies: from primary particles to agglomerate

       G. Orts-Gil, K. Natte, D.Drescher, H.Bresch, A.Mantion, J.Kneipp, W. Österle: J. Nanopart. Res. , 2011, 13, 1593-1604

1. Toxicity of amorphous silica nanoparticles on eukaryotic cell model is determined by particle agglomeration and serum proteins adsorption effects

      D.Drescher, G. Orts-Gil, G.Laube, K. Natte , R.W.Veh , W. Österle , J.Kneipp: Anal. Bioanal. Chem. , 2011, 400,1367-1373