66. Dearomative selective reduction of structurally diverse N-heteroarenes enabled by a homogeneous titanium catalyst
T. Bhatt a, V. Suman a, M. Choudhary b, S. K. Singh b,K. Natte*: J. catal. 2025 [accepted]
Embedded Files
65. Accessing Structurally Diverse Aryl Difluoromethyl Ethers with Bromo(difluoro)acetic Acid
S. Kumawat, K. Natte*: Chem. Comm. 2024, 60, 13935-13938
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
51. Lignin Residue-Derived Carbon-Supported Nanoscale Iron Catalyst for the Selective Hydrogenation of Nitroarenes and Aromatic Aldehydes.
N. Sarki, R. Kumar, B. Singh, A. Ray, G. Naik, K. Natte,* A. Narani: ACS Omega 2022, 23, 19804–19815
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
Page updated
Report abuse