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More Publication of Utpal Bora
Konwar, D., Sarma, P., Borah, J. C., and Bora, U. , Halogen bonding assisted site-selective C-3 triaryl methylation of indoles and N-triaryl methylation of imidazoles, Organic & Biomolecular Chemistry, 21, 6197-6204, 2023, 3.890, Click Here (DOI)
KONWAR, D., Saikia, R., Kalita, R., Das, M. R., and Bora, U, Minimizing base-stoichiometry in Pd (0)/g-C3N4O catalyzed Suzuki-Miyaura cross-coupling reaction, New Journal of Chemistry, 47, 17758-17768, 2023, 3.3, Click Here (DOI)
Saikia, R., Das, S., Almin, A., Mahanta, A., Sarma, B., Thakur, A. J., and Bora, U., N, N’− dimethylurea as an efficient ligand for the synthesis of pharma-relevant motifs through Chan− Lam cross-coupling strategy, Organic & Biomolecular Chemistry, 21, 3143-3155, 2023, 3.890, Click Here (DOI)
Bhattacharjee, P., Dewan, A., Boruah, P. K., Das, M. R., Mahanta, S. P., Thakur, A. J., and Bora, U., Bimetallic Pd-Ag nanoclusters decorated micro-cellulose bio-template towards efficient catalytic Suzuki-Miyaura coupling reaction of nitrogen-rich heterocycles, Green Chemistry, 24(18), 7208-7219, 2022, 10.36 , Click Here (DOI)
Saikia, R., Boruah, P. K., Ahmed, S. M., Das, M. R., Thakur, A. J., and Bora, U., An avenue to Chan-Lam N-arylation by Cu (0) nanoparticles immobilized graphitic carbon-nitride oxide surface, Applied Catalysis A: General, 643, 118767, 2022, 5.706, Click Here (DOI)
Bora, P., Konwar, D., Dewan, A., Das, M. R., and Bora, U., Bio-Carbon Layered CuO Catalysed Decarboxylative Alkenylation of Cyclic Ethers, New Journal of Chemistry, 46, 12551-12557, 2022, 3.3, Click Here (DOI)
Sarmah, M., Sarmah, D., Dewan, A., Bora, P., Boruah, P. K., Das, M. R., Bharali, P., and Bora, U., Dual Responsive Sustainable Cu2O/Cu Nanocatalyst for Sonogashira and Chan-Lam Cross-Coupling Reactions, Catalysis Letters, 1-15, 2022, 2.936 , Click Here (DOI)
Sarmah, D., Saikia, R., and Bora U., An attractive avenue to Chan-Lam cross-coupling: Scope and developments under Ni-catalysis, Tetrahedron, 104, 132567, 2022, 2.457, Click Here (DOI)
Das, S. K., Dewan, A., Deka, P., Saikia, R., Thakuria, S., Deka, R. C., Thakur, A. J., and Bora, U., Biogenic palladium nanostructures for Suzuki-Miyaura and Sonogashira cross-coupling reaction under mild reaction conditions, Current Research in Green and Sustainable Chemistry, 5, 100301, 2022, 4.714, Click Here (DOI)
Bhattacharjee, P., and Bora, U., Organocatalytic dimensions to the C–H functionalization of the carbocyclic core in indoles: a review update, Organic Chemistry Frontiers, 8(10), 2343-2365, 2021, 8(10), 2343-2365, Click Here (DOI)
Saikia, R., Park, K., Masuda, H., Itoh, M., Yamada, T., Sajiki, H., Mahanta, S. P., Thakur, A. J., and Bora, U., Revisiting the synthesis of aryl nitriles: A pivotal role of CAN, Organic & Biomolecular Chemistry, 19(6), 1344-1351, 2021, 3.89, Click Here (DOI)
Dewan, A., Sarmah, M., Bharali, P., Thakur, A. J., Boruah, P. K., Das, M. R., and Bora, U., Pd nanoparticles-loaded honeycomb-structured bio-nanocellulose as a heterogeneous catalyst for heteroaryl cross-coupling reaction, ACS Sustainable Chemistry & Engineering, 9(2), 954-966, 2021, 9.224, Click Here (DOI)
Sarmah, D., Borah, K. K., and Bora, U., Aqueous extracts of biomass ash as an alternative class of Green Solvents for organic transformations: A review update, Sustainable Chemistry and Pharmacy, 24, 100551, 2021, 5.464, Click Here (DOI)
Bora, P., Bora, B., and Bora, U. , Recent developments in synthesis of catechols by Dakin oxidation, New Journal of Chemistry, 45(37), 17077-17084., 2021, 3.3, Click Here (DOI)
Sarmah, D., Tahu, M., and Bora, U., Recent advances in the synthesis of indoles via C–H activation aided by N–N and N–S cleavage in the directing group, Applied Organometallic Chemistry, 35(11), e6390, 2021, 4.072, Click Here (DOI)
Dewan, A., Sarmah, M., Bhattacharjee, P., Bharali, P., Thakur, A. J., and Bora, U., Sustainable nano fibrillated cellulose supported in situ biogenic Pd nanoparticles as heterogeneous catalyst for C–C cross coupling reactions, Sustainable Chemistry and Pharmacy, 23, 100502., 2021, 5.464, Click Here (DOI)
Konwar, D., and Bora, U., Recent Developments in Transition‐Metal‐Catalyzed Regioselective Functionalization of Imidazo [1, 2‐a] pyridine, ChemistrySelect, 6(11), 2716-2744, 2021, 2.307, Click Here (DOI)
Mahanta, A., Dutta, A., Thakur, A. J., and Bora, U., Biocatalysis with Baker's yeast: A green and sustainable approach for C–B bond cleavage of aryl/heteroarylboronic acids and boronate esters at room temperature, Sustainable Chemistry and Pharmacy, 19, 100363, 2021, 5.464, Click Here (DOI)
Mahanta, A., Thakur, A. J., and Bora, U. , Effective utilization of basic nature of WEB in copper catalyzed Chan-Lam N-arylation reaction under ligand free conditions, Current Research in Green and Sustainable Chemistry, 4, 100093, 2021, 4.71, Click Here (DOI)
Das, S. K., Bhattacharjee, P., Sarmah, M., Kakati, M., and Bora, U. , A sustainable approach for hydration of nitriles to amides utilising WEB as reaction medium, Current Research in Green and Sustainable Chemistry, 4, 100071, 2021, 4.71, Click Here (DOI)
Bhattacharjee, P., Boruah, P. K., Das, M. R., and Bora, U. , Direct C–H bond activation: palladium-on-carbon as a reusable heterogeneous catalyst for C-2 arylation of indoles with arylboronic acids, New Journal of Chemistry, 44(19), 7675-7682, 2020, 3.3, Click Here (DOI)
Das, S. K., Laskar, K., Konwar, D., Sahoo, A., Saikia, B. K., and Bora, U. , Repurposing fallen leaves to bio-based reaction medium for hydration, hydroxylation, carbon-carbon and carbon-nitrogen bond formation reactions, Sustainable Chemistry and Pharmacy, 15, 100225, 2020, 5.464, Click Here (DOI)
Sarmah, M., Dewan, A., Boruah, P. K., Das, M. R., and Bora, U., Intercalation of copper salt to montmorillonite K‐10 and its application as a reusable catalyst for Chan–Lam cross‐coupling reaction, Applied Organometallic Chemistry, 34(4), e5554, 2020, 4.072, Click Here (DOI)
Sarmah, D., and Bora, U. , Methylene Surrogates for the Synthesis of 3, 3’‐Diindolylmethanes, ChemistrySelect, 5(28), 8577-8603, 2020, 2.307, Click Here (DOI)
Konwar, D., and Bora, U., Free Radical Triggered Convenient Synthesis of Bis (indolyl) methane with Potassium Peroxodisulfate as Catalyst, ChemistrySelect, 5(25), 7460-7466, 2020, 2.307, Click Here (DOI)
Gohain, M., Bardhan, P., Laskar, K., Sarmah, S., Mandal, M., Bora, U., Kalita, M. C., Goud, V. V. and Deka, D., Rhodotorula mucilaginosa: A source of heterogeneous catalyst for biodiesel production from yeast single cell oil and waste cooking oil, Renewable Energy, 160, 220-230, 2020, 8.634, Click Here (DOI)
Gohain, M., Laskar, K., Paul, A. K., Daimary, N., Maharana, M., Goswami, I. K., Hazarika, K., Bora, U., and Deka, D. , Carica papaya stem: A source of versatile heterogeneous catalyst for biodiesel production and C–C bond formation, Renewable Energy, 147, 541-555, 2020, 8.634, Click Here (DOI)
Gohain, M., Laskar, K., Phukon, H., Bora, U., Kalita, D., and Deka, D. , Towards sustainable biodiesel and chemical production: Multifunctional use of heterogeneous catalyst from littered Tectona grandis leaves, Waste Management, 102, 212-221, 2020, 8.816, Click Here (DOI)
Hatiboruah, D., Das, T., Chamuah, N., Rabha, D., Talukdar, B., Bora, U., Ahamad K.U., and Nath, P. , Estimation of trace-mercury concentration in water using a smartphone, Measurement, 154, 107507, 2020, 5.131, Click Here (DOI)
Saikia, R., Dey Baruah, S., Deka, R. C., Thakur, A. J., and Bora, U. , An insight into nitromethane as an organic nitrile alternative source towards the synthesis of aryl nitriles, European Journal of Organic Chemistry, 2019(36), 6211-6216, 2019, 3.261, Click Here (DOI)
Laskar, K., Paul, S., and Bora, U., Cellulose as recyclable organocatalyst for ipso-hydroxylation of arylboronic acids, Tetrahedron Letters, 60(38), 151044, 2019, 2.032, Click Here (DOI)
Laskar, K., Bhattacharjee, P., Gohain, M., Deka, D., and Bora, U., Application of bio-based green heterogeneous catalyst for the synthesis of arylidinemalononitriles, Sustainable Chemistry and Pharmacy, 14, 100181, 2019, 5.464, Click Here (DOI)
Bhattacharjee, P., and Bora, U. , Molecular iodine-catalyzed selective C-3 benzylation of indoles with benzylic alcohols: a greener approach toward benzylated indoles., ACS omega, 4(7), 11770-11776, 2019, 4.132, Click Here (DOI)
Mahanta, A., Gour, N. K., Sarma, P. J., Borah, R. K., Raul, P. K., Deka, R. C., Thakur, A, J., Bora, U and Bora, U., A convenient room temperature ipso‐nitration of arylboronic acid catalysed by molecular iodine using zirconium oxynitrate as nitrating species: An experimental and theoretical investigation, Applied Organometallic Chemistry, 33(8), e4951, 2019, 4.072, Click Here (DOI)
Sarmah, M., Neog, A. B., Boruah, P. K., Das, M. R., Bharali, P., and Bora, U. , Effect of substrates on catalytic activity of biogenic palladium nanoparticles in C–C cross-coupling reactions, ACS omega, 4(2), 3329-3340, 2019, 4.132, Click Here (DOI)
Dewan, A., Sarmah, M., Thakur, A. J., Bharali, P., and Bora, U. , Greener biogenic approach for the synthesis of palladium nanoparticles using papaya peel: An eco-friendly catalyst for C–C coupling reaction, ACS omega, 3(5), 5327-5335, 2018, 4.132, Click Here (DOI)
Mahanta, A., Raul, P. K., Saikia, S., Bora, U., and Thakur, A. J., Methanol aided synthesis of PdNPs decorated on montmorillonite K 10 and its implication in Suzuki Miyaura type cross coupling reaction under base free condition, Applied Organometallic Chemistry, 32(3), e4192, 2018, 4.072, Click Here (DOI)
Das, S. K., Deka, P., Chetia, M., Deka, R. C., Bharali, P., and Bora, U. , Spherical CuO nanoparticles as catalyst for Chan–lam cross-coupling reaction under base free condition, Catalysis Letters, 148(2), 547-554, 2018, 2.936, Click Here (DOI)
Das, S. K., Bhattacharjee, P., and Bora, U., Ascorbic Acid as a Highly Efficient Organocatalyst for ipso‐Hydroxylation of Arylboronic Acid, ChemistrySelect, 3(7), 2131-2134, 2018, 2.307, Click Here (DOI)
Begum, T., Mondal, M., Borpuzari, M. P., Kar, R., Gogoi, P. K., and Bora, U. , Palladium‐on‐Carbon‐Catalyzed Coupling of Nitroarenes with Phenol: Biaryl Ether Synthesis and Evidence of an Oxidative‐Addition‐Promoted Mechanism, European Journal of Organic Chemistry, 2017(22), 3244-3248, 2017, 3.261, Click Here (DOI)
Begum, T., Mondal, M., Borpuzari, M. P., Kar, R., Kalita, G., Gogoi, P. K., and Bora, U. , An immobilized symmetrical bis-(NHC) palladium complex as a highly efficient and recyclable Suzuki–Miyaura catalyst in aerobic aqueous media, Dalton Transactions, 46(2), 539-546., 2017, 4.569, Click Here (DOI)
Mondal, M., Begum, T., and Bora, U., Chemoselective acyl C–O bond activation in esters for Suzuki–Miyaura coupling, Organic Chemistry Frontiers, 4(7), 1430-1434, 2017, 5.456, Click Here (DOI)
Sarmah, M., Mondal, M., Gohain, S. B., and Bora, U., Gallic acid-derived palladium (0) nanoparticles as in situ-formed catalyst for Sonogashira cross-coupling reaction in ethanol under open air, Catalysis Communications, 90, 31-34, 2017, 3.51, Click Here (DOI)
Sarmah, M., Dewan, A., Thakur, A. J., and Bora, U. , Extraction of base from Eichhornia crassipes and its implication in Palladium‐Catalyzed Suzuki Cross‐Coupling Reaction, ChemistrySelect, 2(24), 7091-7095, 2017, 2.307, Click Here (DOI)
Sarmah, M., Mondal, M., and Bora, U. , Agro‐waste extract based solvents: emergence of novel green solvent for the design of sustainable processes in catalysis and organic chemistry, ChemistrySelect, 2(18), 5180-5188, 2017, 2.307, Click Here (DOI)
Das, S. K., Sarmah, M., and Bora, U., An ambient temperature Sonogashira cross-coupling protocol using 4-aminobenzoic acid as promoter under copper and amine free conditions, Tetrahedron Letters, 58(22), 2094-2097, 2017, 2.032, Click Here (DOI)
Begum, T., Gogoi, P. K., and Bora, U. , Photocatalytic degradation of crystal violet dye on the surface of Au doped TiO2 nanoparticle, Indian Journal of Chemical Technology, 24, 97-101, 2017, 0.76, Click Here (DOI)
Borah, R. K., Mahanta, A., Dutta, A., Bora, U., and Thakur, A. J. , A green synthesis of palladium nanoparticles by Sapindus mukorossi seed extract and use in efficient room temperature Suzuki–Miyaura cross‐coupling reaction, Applied Organometallic Chemistry, 31(11), e3784, 2017, 4.072, Click Here (DOI)
Baruah, J., Gogoi, K., Dewan, A., Borah, G., and Bora, U. , Carbothioamide as Highly Efficient Ligand for Copper‐catalyzed Room Temperature Chan–Lam Cross‐Coupling Reaction, Bulletin of the Korean Chemical Society, 38(10), 1203-1208, 2017, 1.241, Click Here (DOI)
Dewan, A., Sarmah, M., Bora, U., and Thakur, A. J., In situ generation of palladium nanoparticles using agro waste and their use as catalyst for copper‐, amine‐and ligand‐free Sonogashira reaction, Applied Organometallic Chemistry, 31(7), e3646, 2017, 4.072, Click Here (DOI)
Gogoi, N., Bora, U., Borah, G., and Gogoi, P. K. , Nanosilica‐anchored Pd (II)‐Schiff base complex as efficient heterogeneous catalyst for activation of aryl halides in Suzuki–Miyaura cross‐coupling reaction in water, Applied Organometallic Chemistry, 31(9), e3686, 2017, 4.072, Click Here (DOI)
Mahanta, A., Hussain, N., Das, M. R., Thakur, A. J., and Bora, U., Palladium nanoparticles decorated on reduced graphene oxide: An efficient catalyst for ligand‐and copper‐free Sonogashira reaction at room temperature, Applied Organometallic Chemistry, 31(8), e3679, 2017, 4.072, Click Here (DOI)
Mondal, M., Begum, T., Gogoi, P. K., and Bora, U., Gallic Acid Derived Palladium (0) Nanoparticles: An In Situ Formed “Green and Recyclable” Catalyst for Suzuki‐Miyaura Coupling in Water, ChemistrySelect, 1(15), 4645-4651, 2016, 2.307, Click Here (DOI)
Mondal, M., Dewan, A., Begum, T., Gogoi, P. K., Thakur, A. J., and Bora, U., Suzuki–Miyaura Cross-Coupling in Aqueous Medium Using Recyclable Palladium/Amide-Silica Catalyst, Catalysis Letters, 146(9), 1718-1728, 2016, 2.936, Click Here (DOI)
Gogoi, N., Gogoi, P. K., Borah, G., and Bora, U. , Grafting of Ru (III) complex onto nanosilica and its implication as heterogeneous catalyst for aerobic oxidative hydroxylation of arylboronic acids, Tetrahedron Letters, 57(36), 4050-4052, 2016, 2.032, Click Here (DOI)
Dewan, A., Sarmah, M., Bora, U., and Thakur, A. J. , A green protocol for ligand, copper and base free Sonogashira cross-coupling reaction, Tetrahedron Letters, 57(33), 3760-3763, 2016, 2.032, Click Here (DOI)
Mahanta, A., Mondal, M., Thakur, A. J., and Bora, U., An improved Suzuki–Miyaura cross-coupling reaction with the aid of in situ generated PdNPs: evidence for enhancing effect with biphasic system, Tetrahedron Letters, 57(29), 3091-3095, 2016, 2.032, Click Here (DOI)
Mondal, M., and Bora, U. , Eco-friendly Suzuki–Miyaura coupling of arylboronic acids to aromatic ketones catalyzed by the oxime-palladacycle in biosolvent 2-MeTHF, New Journal of Chemistry, 40(4), 3119-3123, 2016, 3.925, Click Here (DOI)
Sarmah, M., Dewan, A., Thakur, A. J., and Bora, U. , Urea as mild and efficient additive for palladium catalyzed Sonogashira cross coupling reaction, Tetrahedron Letters, 57(8), 914-916, 2016, 2.032, Click Here (DOI)
Sarmah, M., Dewan, A., Mondal, M., Thakur, A. J., and Bora, U. , Analysis of the water extract of waste papaya bark ash and its implications as an in situ base in the ligand-free recyclable Suzuki–Miyaura coupling reaction, RSC advances, 6(34), 28981-28985, 2016, 4.036, Click Here (DOI)
Dewan, A., Bharali, P., Bora, U., and Thakur, A. J. , Starch assisted palladium (0) nanoparticles as in situ generated catalysts for room temperature Suzuki–Miyaura reactions in water, RSC advances, 6(14), 11758-11762, 2016, 4.036, Click Here (DOI)
Gogoi, N., Begum, T., Dutta, S., Bora, U., and Gogoi, P. K. , Rice husk derived nanosilica supported Cu (II) complex: an efficient heterogeneous catalyst for oxidation of alcohols using TBHP., RSC advances, 5(115), 95344-95352, 2015, 4.036, Click Here (DOI)
Raul, P. K., Mahanta, A., Bora, U., Thakur, A. J., and Veer, V., In water homocoupling of arylboronic acids using nano-rod shaped and reusable copper oxide (II) catalyst at room temperature, Tetrahedron letters, 56(51), 7069-7073, 2015, 2.032, Click Here (DOI)
Kumar Borah, R., Jyoti Saikia, H., Kumar Das, V., and Jyoti Thakur, A. , Biosynthesis of poly (ethylene glycol)-supported palladium nanoparticles using Colocasia esculenta leaf extract and their catalytic activity for Suzuki–Miyaura cross-coupling reactions, RSC advances, 5(89), 72453-72457, 2015, 4.036, Click Here (DOI)
Sarmah, G., Mondal, M., and Bora, U. , Alcoholic solvent‐assisted ligand‐free room temperature Suzuki–Miyaura cross‐coupling reaction, Applied Organometallic Chemistry, 29(8), 495-498, 2015, 4.072, Click Here (DOI)
Sarmah, G., and Bora, U., Simple aminobenzoic acid promoted palladium catalyzed room temperature Suzuki–Miyaura cross-coupling reaction in aqueous media, Tetrahedron Letters, 56(22), 2906-2909, 2015, 2.032, Click Here (DOI)
Begum, T., Mondal, M., Gogoi, P. K., and Bora, U., Palladium-Schiff-base-silica framework as a robust and recyclable catalyst for Suzuki–Miyaura cross-coupling in aqueous media, RSC Advances, 5(48), 38085-38092, 2015, 4.036, Click Here (DOI)
Gogoi, A., Dewan, A., Borah, G., and Bora, U., A palladium salen complex: An efficient catalyst for the Sonogashira reaction at room temperature, New Journal of Chemistry, 39(5), 3341-3344, 2015, 3.925, Click Here (DOI)
Mahanta, A., Adhikari, P., Bora, U., and Thakur, A. J. , Biosilica as an efficient heterogeneous catalyst for ipso-hydroxylation of arylboronic acids, Tetrahedron Letters, 56(14), 1780-1783, 2015, 2.032, Click Here (DOI)
Begum, T., Gogoi, A., Gogoi, P. K., and Bora, U., Catalysis by mont K-10 supported silver nanoparticles: a rapid and green protocol for the efficient ipso-hydroxylation of arylboronic acids, Tetrahedron Letters, 56(1), 95-97, 2015, 2.032, Click Here (DOI)
Gogoi, A., Dewan, A., and Bora, U. , A highly efficient copper and ligand free protocol for the room temperature Sonogashira reaction, RSC advances, 5(1), 16-19, 2015, 4.036, Click Here (DOI)
Gogoi, P. K., Begum, T., Borthakur, B., Das, G., Bora, U., and Kumar, A. , Green synthesis of silver nanoparticles using leaf extract of Phlogacanthus thyrsiformis and evaluation of their antibacterial and catalytic activity, National Academy Science Letters, 38, 231-234, 2015, 0.649, Click Here (DOI)
Mondal, M., Bharadwaj, S. K., and Bora, U. , O-Arylation with nitroarenes: metal-catalyzed and metal-free methodologies. , New Journal of Chemistry, 39(1), 31-37., 2014, 3.925, Click Here (DOI)
Gogoi, A., Chutia, S. J., Gogoi, P. K., and Bora, U. , A highly efficient heterogeneous montmorillonite K‐10‐supported palladium catalyst for Suzuki–Miyaura cross‐coupling reaction in aqueous medium, Applied Organometallic Chemistry, 28(11), 839-844, 2014, 4.072, Click Here (DOI)
Sarmah, G., Bharadwaj, S. K., Dewan, A., Gogoi, A., and Bora, U., An efficient and reusable vanadium based catalytic system for room temperature oxidation of alcohols to aldehydes and ketones, Tetrahedron Letters, 55(36), 5029-5032, 2014, 2.032, Click Here (DOI)
Sarmah, G., Bharadwaj, S. K., Dewan, A., Gogoi, A., and Bora, U. , An efficient and reusable vanadium based catalytic system for room temperature oxidation of alcohols to aldehydes and ketones, Tetrahedron Letters, 55(36), 5029-5032, 2014, 2.032, Click Here (DOI)
Mondal, M., and Bora, U., O-Aryloxime ether analogues as novel and efficient ligands for palladium-catalyzed Suzuki–Miyaura coupling in water, Tetrahedron Letters, 55(19), 3038-3040, 2014, 2.032, Click Here (DOI)
Boruah, P. R., Koiri, M. J., Bora, U., and Sarma, D., A new recyclable/reusable ionic liquid/LiCl system for Suzuki–Miyaura cross coupling reactions, Tetrahedron Letters, 55(15), 2423-2425, 2014, 2.032, Click Here (DOI)
Mondal, M., and Bora, U., Ligandless heterogeneous palladium: an efficient and recyclable catalyst for Suzuki‐type cross‐coupling reaction, Applied Organometallic Chemistry, 28(5), 354-358., 2014, 4.072, Click Here (DOI)
Dewan, A., Bora, U., and Borah, G. , A simple and efficient tetradentate Schiff base derived palladium complex for Suzuki–Miyaura reaction in water, Tetrahedron Letters, 55(10), 1689-1692., 2014, 2.032, Click Here (DOI)
Gogoi, K., Dewan, A., Gogoi, A., Borah, G., and Bora, U., Boric acid as highly efficient catalyst for the synthesis of phenols from arylboronic acids, Heteroatom Chemistry, 25(2), 127-130, 2014, 1.32, Click Here (DOI)
Dewan, A., Buragohain, Z., Mondal, M., Sarmah, G., Borah, G., and Bora, U. , Acetanilide palladacycle: an efficient catalyst for room‐temperature Suzuki–Miyaura cross‐coupling reaction, Applied Organometallic Chemistry, 28(4), 230-233, 2014, 4.072, Click Here (DOI)
Gogoi, A., Sarmah, G., Dewan, A., and Bora, U., Unique copper–salen complex: an efficient catalyst for N-arylations of anilines and imidazoles at room temperature, Tetrahedron Letters, 55(1), 31-35, 2014, 2.032, Click Here (DOI)
Borah, G., Boruah, D., Sarmah, G., Bharadwaj, S. K., and Bora, U. , The development of phosphinoamine–Pd (II)–imidazole complexes: implications in room‐temperature Suzuki–Miyaura cross‐coupling reaction, Applied Organometallic Chemistry, 27(12), 688-694, 2013, 4.072, Click Here (DOI)
Mondal, M., and Bora, U. , Recent advances in manganese (III) acetate mediated organic synthesis, RSC advances, 3(41), 18716-18754, 2013, 4.036, Click Here (DOI)
