Welcome to LDR Research group, Synthetic Organic Chemistry     Welcome to LDR Research group, Synthetic Organic Chemistry

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38. Immunomodulatory and anti-inflammatory and anticancer activities of porphyran, a sulfated galactan, B.  Pradhan,  J.-S.  Ki  and L. Rout,, Carbohydrate Polymers, 2023,, 301, Part A, 120326  (IF 11.0) https://doi.org/10.1016/j.carbpol.2022.120326

 
 

37. CuMoO4 Catalyzed  Csp 2-Se Cross-Coupling of Aryl Bromide and Iodide with Diaryldiselenides in Water; P Choudhury,  A. K. Pradhan, S. Jena, B. K.  Sahoo, S. K. Sahu, P.  K. Behera, P. Behera,  A. Swain,and Dr.  Laxmidhar Rout , 2022, https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.202201194

36. Transition Metal Catalysed C-S Cross-Coupling Reactions at Room Temperature.,  Pradyota Kumar Behera,a Prabhupada Choudhurya Papita BeheraAmlan Swain,a Amit Kumar Pradhan,a and Laxmidhar Routa*  Chemistry Select 2022, 2022, 7, 41, e202202919,  https://doi.org/10.1002/slct.202202919  (IF 2.89)


35. MTP18 inhibition triggers mitochondrial hyperfusion to induce apoptosis through ROS-mediated lysosomal membrane permeabilization-dependent pathway in oral cancer; D. P. Panigrahi, S. Patra, B. P. Behera, P. K. Behera, S. Patil, B.S. Patro,L.  Rout, *,I. Sarangi *, S. K. Bhutia,* Free radical Biology and Medicine, 2022,  2022, 190, 307. https://doi.org/10.1016/j.freeradbiomed.2022.08.019 (In Press).   (IF 8.01)


 

34. Efficient Oxygen Bridged Bimetallic CuSeO3.2H2O Catalyzed  (CSP2-CSp) Sonogasira  Cross-Coupling of  Terminal Aryl Acetylene with Haloarenes, S. K. Sahu, P. Choudhury, P. K. Behera, T. Bisoyi, R. R. Sahoo, A. Bisoyi, K. R. Gorantala, B.S. Mallick, M. Mohapatra and. L. Rout  , New. J. Chem, 2022;  46, 1650-1657. 10.1039/D1NJ04485K  (IF 3.6)


33. Strategy for Synthesis of Structural Analogues of Artemisinin, S.K. Sahu, P. K. Behera, M. C. Maity, P. Behera, A. Swain, R. K. Sahu, S. Panda  and L. Rout, Res. J. Berham. Univ. 2021, 3, 69-82, 2021, ISSN 2250-1681


32. Recent advance in [3+2] cycloa ddition of allene with 1,3-carbonyl ylide; Rh(II) catalyzed access to bridged polyoxocarbocyles; S. K. Sahu, P. K. Behera,  P. Choudhury,  M. Sethi, S. Jena, and L. Rout, New. J. Chem, 2021, 45, 11018-11029;  10.1039/D1NJ02034J , (IF 3.6).


31.Oxygen bridged bimetallic CuMoO4 nanocatalyst for benzylic alcohol  oxidation; mechanism and DFT  study; P. K. Behera,  P. Choudhury,  S K. Sahu, R. R. Sahu, A. N. Harvat, C. McNulty, A.  Stitgen, J.  Scanlon, M.  Kar, and Prof. L. Rout, A. J. Org. Chem. 2021, 10, 1117-1122;  DOI: 10.1002/ajoc.202100192  (IF 4.0)

30. Dehydrogenative oxidation of aryl methanol using oxygen bridged [Cu-O-Se] bimetallic catalyst; P.  Choudhury,  P.  K. Behera,  S. K. Sahu,  T.  Bisoyi, R. R. Sahu,  S.  R.  Prusty,  A. Stitgen,  J. Scanlon, Prof. L.  Rout, New. J. Chem, 2021, 45, 5775-5779. https://doi.org/10.1039/D1NJ00712B(IF 3.6)

29. Recent Advances in Transition-Metal-Mediated Csp2-B and Csp2-P Cross-Coupling Reactions, Laxmidhar Rout and Tharmalingam Punniyamurthy, Coordination Chemistry Review, 2021, 413, 213675.  https://doi.org/10.1016/j.ccr.2020.213675, (Impact factor 22)

28.Chemotherapeutic efficacy of curcumin and resveratrol against cancer: Chemoprevention, chemoprotection, drug synergism and clinical pharmacokinetics,  S.  Patra; B. Pradhan; R.  Nayak; C.  Behera; L. Rout, M. Jena, T. Efferth, S. K. Bhutia,Seminars in Cancer Biology, 2021, 73, 310-320; https://doi.org/10.1016/j.semcancer.2020.10.010  (Impact factor 15).

27. Developments in chemistry and biological application of cotarnine & its analogs, Sahu, S. K.   Behera, P. K.  Panda, S.  Choudhury, P. and Rout, L. Tetrahedron 2020, 76,50, 131663.  ; https://doi.org/10.1016/j.tet.2020.131663 (IF 2.8)

26. Strategy and Problems for Synthesis  of Antimalaria Artemisinin (Qinghaosu);  Santosh Kumar Sahu,  Pradyota Kumar Behera, Prabhupada Choudhury,  Subhalaxmi Panda and  Laxmidhar Rout,  Chemistry Select 2020, 29, 12333-12344; https://doi.org/10.1002/slct.202002885  (IF 2.3)

 

25. Bimetallic  BaMoO4 Nanoparticle for  C-S Cross-Coupling of Thiols  with Haloarene. Subhalaxmi Panda, Pradyota  Kumar Behera,  Santosh Kumar Sahu, Reba Panigrahi, Bamakanta Garnaik and Laxmidhar Rout,  New J. Chem 2020, 44, 2500-2504; https://doi.org/10.1039/C9NJ05581A  (IF 3.6)

 

 24.CuMoO4 Bimetallic Nanoparticles, An  Efficient Catalyst  for Room Temperature C-S Cross-coupling of Thiols and Haloarenes,  Reba Panigrahi, Santosh Kumar Sahu, Pradyota Kumar Behera, Subhalaxmi Panda, and  Prof. Laxmidhar Rout,  Chemistry Eur. J. 2020, 24, 620-624.https://org/doi/10.1002/chem.201904801  (IF 5.9).

 

 23.Recyclable Bimetallic CuMoO4 Nanoparticle for  C-N Cross-Coupling Reaction Under Mild Condition. Reba Panigrahi,  Subhalaxmi Panda, Pradyota  Kumar Behera,  Santosh Kumar Sahu and  Dr. Laxmidhar Rout. New J. Chem 2019,  43, 19274.  https://doi.org/10.1039/C9NJ04436A (IF 3.6).

22.Synthesis of Acyl Derivatives of Cotarnine, Organic Synthesis Database Online, (Editor: A. S. Kendee, and J. S. Freeman) . Dr. Laxmidhar Rout,   B.Emmanuel, and Prof. A. K. Sahoo,  2019, Volume 95., Org. Syn. 95, 455. https://doi.org/10.1002/0471264229.os095.30

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21.Metal Free Activation of C(SP3)-H Bond, Practical and Rapid Synthesis of Privileged 1-Substituted-1,2,3,4-Tetrahydroisoquinolines,  S. K. Choudhury, P. Rout, J-C. Florent, L. Johannes, E. Bertounesque,  Prof. Laxmidhar Rout, Eur J. Org. Chem. 2017,  35, 5275-5292; https://doi.org/10.1002/ejoc.201700471  (IF 4.0);

20. Metal-Free Activation of a C(sp)−H Bond of Aryl Acetylenes Laxmidhar Rout, Dr. Dr. Jean-Claude Florent, Dr. Ludger Johannes, Santosh Kumar Choudhury, Joe Scanlon and  Emmanuel Bertounesque  Chem. - A Europ. J. 2016,  22, 14812–14815,   https://doi.org/10.1002/chem.201603003 (IF 5.9)

19. Activation of a Carbonyl Compound by Halogen Bonding;  S. H. Jungbauer,  S.M. Walter, S. Schinder,  L. Rout,  F. Kniep  and S. M. Huber, Chem. Commun., 2014, 50, 6281-6284.https://doi.org/10.1039/C4CC03124E  (IF 6.3)

18. Multidentate Halogen-Bond Donors as Lewis Acidic Activators or Catalysts in Halide Abstraction Reactions;  S. H. Jungbauer,  F. Kniep, S.M. Walter, S. Schinder,  L. Rout, and S. M. Huber; Synlett, 2013, 24, 2624. DOI: 10.1055/s-0033-1338981

 

17. 5-Iodo-1,2,3-triazolium-based multidentate halogen-bond donors as activating reagents,   F. Kniep, L. Rout, S.M. Walter, H. K. V. Bensch, S. H. Jungbauer, E. Herdtweck and S. M. Huber. Chem. Comm,2012, 48, 9299.

16. Isothermal Calorimetric Titrations on Charge-Assisted Halogen Bonds: Role of Entropy, Counterions, Solvent, and Temperature   Sebastian M. Walter, Florian Kniep, Laxmidhar Rout, Franz P. Schmidtchen, Eberhardt Herdtweck, Stefan M. Huber. J. Am. Chem. Soc. 2012134, 8507-8512.https://doi.org/10.1021/ja2119207  (IF 15.4)

15. Synthesis of a-Arylphosphonates Using Copper-Catalyzed a-Arylation and Deacylative  a-Arylation of b-Ketophosphonates.  L. Rout, S. Regati and C. G. Zhao, Adv. Synth. Catal. 2011, 353, 3340.   https://doi.org/10.1002/adsc.201100605 (IF 5.8) 

14.Organocatalytic Highly Enantioselective Synthesis of b-Formyl-a-hydroxyphosphonates;   S. Perera, V. K. Naganaboina, L.Wang, B.  Zhang, Q. Guo, L. Rout and C.-G. Zhao. Adv. Synth. Catal. 2011, 353, 1729.  https://doi.org/10.1002/adsc.201000835  (IF 5.8)

 13 Allene Carboxylates as Dipolarophiles in Rh‐Catalyzed Carbonyl Ylide Cycloadditions.    L. Rout and A. M. Harned., Chem. Eur. J.  2009, 15, 12926.  https://doi.org/10.1002/chem.200902208  (IF 5.7)

 12. CuO Nanoparticles Catalyzed C−NC−O, and C−S Cross-Coupling Reactions: Scope and Mechanism.S. Jammi,  S. Sakthivel, L. Rout, T. Mukherjee, S. Mandal, R. Mitra, P. Saha and T. Punniyamurthy,  J. Org. Chem. 2009, 74, 1971.   https://doi.org/10.1021/jo8024253  (IF 4.3)

 11. Synthesis, Structure, and Application of Self-Assembled Copper(II) Aqua Complex by H-Bonding for Acceleration of the Nitroaldol Reaction in Water;   S. Jammi, Md A. Ali, S. Sakthivel, L. Rout, and T. Punniyamurthy . Chem. Asian. J. 2009, 4, 314. https://doi.org/10.1002/asia.200800339  (IF 4.6)

10.Synthesis, Structure and Application of Chiral Copper(II) Polymers for Asymmetric Acylation  of Secondary Alcohols.    S. Jammi, L. Rout, P. Saha, V. K. Akhilagunta, S. Sanyasi and T. Punniyamurthy, InorgChem.  2008, 12, 5093. https://doi.org/10.1021/ic800228c  (IF 5.1)

9. Efficient Ligand-Free Nickel-Catalyzed C-S Cross-Coupling of Thiols with Aryl Iodides.    S. Jammi, P. Barua, L. Rout, P. Saha and T. Punniyamurthyhttps://doi.org/10.1016/j.tetlet.2007.12.118, Tetrahedron. Lett. 2008, 49,1484.  (IF 2.8)

8.Efficient Copper(I) Catalyzed C-S Cross-Coupling of Thiols with Aryl Halides in Water;    L. Rout, P. Saha and T. Punniyamurthy, Eur. J. Org. Chem. 2008, 640.  https://doi.org/10.1002/ejoc.200700978   (IF 3.021)

7.Recent Advances in Copper-Catalyzed Oxidation of Organic Compounds.  T. Punniyamurthy and L. RoutCoord. Chem. Rev.2008252,134. https://doi.org/10.1016/j.ccr.2007.04.003, (IF 22.0)

6.Cadmium(II) Catalyzed C-N Cross-Coupling of Amines with Aryl Iodides.  L. Rout, S. Jammi and T. PunniyamurthyAdv. Synth. Catal. 2008, 350, 395. 

 https://doi.org/10.1002/adsc.200700480 (IF 5.8)

5.Efficient CuO Nanoparticle Catalyzed C-S Cross Coupling of Thiols with Iodobenzene;   L. Rout, T. K. Sen and T. Punniyamurthy, Angew. Chem. Int. Ed. Eng 2007, 46, 5583. https://doi.org/10.1002/anie.200701282  (IF 15.34)

4.Novel CuO Nanoparticle Catalyzed  C- Cross-Coupling of Amines with Iodobenzene.;   L. Rout, S. Jammi and T. Punniyamurthy, Org. Lett. 2007, 9, 3397.https://doi.org/10.1021/ol0713887  (IF 6.5)

3.Chiral Linear Polymers Bonded Alternatively with Salen and 1,4-Dialkoxy-2,6-diethynylbenzene: Synthesis and Application to Diethylzinc Addition to AldehydesS. Jammi, L. Rout and T. Punniyamurthy, Tetrahedron: Asymmetry 2007,17,2016.  https://doi.org/10.1016/j.tetasy.2007.09.004  (IF 2.6)

2.Vanadium-Catalyzed Selective Oxidation of Alcohols to Aldehydes and Ketones with t-BuO2H;  L. Rout and T. Punniyamurthy, Adv. Synth. Catal. 2007349, 846. 
 https://doi.org/10.1002/adsc.200600397  (IF 5.8)

1.Silica-Supported Vanadium-Catalyzed N-Oxidation of Tertiary Amines with Aq. H2O2.   L. Rout and T. Punniyamurthy, Adv. Synth. Catal.  2005, 347, 1958.  https://doi.org/10.1002/adsc.200505166  (IF 5.8)

 

 

 

 

 

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