Year |
Citation |
Score |
2024 |
Banerjee D, Sk M, Saifi S, Bera S, Ghosh A, Aijaz A. Reusable Ni-immobilized MOF Catalyst for Dehydrogenation of N-heterocycles Under Milder Conditions. Chemistry (Weinheim An Der Bergstrasse, Germany). e202404219. PMID 39656157 DOI: 10.1002/chem.202404219 |
0.816 |
|
2024 |
Kabadwal LM, Haldar S, Banerjee D. Sequential One-Pot Transformation to R-CF-Embedded 1,5-Diketones Enabled by Nickel: Access to 4-Perfluoroalkylpyridines. Organic Letters. 26: 9299-9304. PMID 39441894 DOI: 10.1021/acs.orglett.4c03478 |
0.826 |
|
2024 |
Bera S, Kabadwal LM, Banerjee D. Harnessing alcohols as sustainable reagents for late-stage functionalisation: synthesis of drugs and bio-inspired compounds. Chemical Society Reviews. PMID 38525675 DOI: 10.1039/d3cs00942d |
0.832 |
|
2024 |
Mullick S, Ghosh A, Banerjee D. Recent advances in cross-coupling of alcohols borrowing hydrogen catalysis. Chemical Communications (Cambridge, England). PMID 38451211 DOI: 10.1039/d4cc00003j |
0.829 |
|
2024 |
Sk M, Haldar S, Bera S, Banerjee D. Recent advances in the selective semi-hydrogenation of alkyne to ()-olefins. Chemical Communications (Cambridge, England). PMID 38251772 DOI: 10.1039/d3cc05395d |
0.803 |
|
2023 |
Bera A, Banerjee D. Recent advances on non-precious metal-catalysed fluorination, difluoromethylation, trifluoromethylation, and perfluoroalkylation of N-heteroarenes. Organic & Biomolecular Chemistry. PMID 37855147 DOI: 10.1039/d3ob01132a |
0.625 |
|
2023 |
Bera A, Ghosh A, Banerjee D. Nickel-Catalyzed Alkylation of Oxindoles with Secondary Alcohols. The Journal of Organic Chemistry. PMID 37161856 DOI: 10.1021/acs.joc.3c00402 |
0.786 |
|
2022 |
Dey G, Saifi S, Sk M, Sinha ASK, Banerjee D, Aijaz A. Immobilizing a homogeneous manganese catalyst into MOF pores for α-alkylation of methylene ketones with alcohols. Dalton Transactions (Cambridge, England : 2003). PMID 36278796 DOI: 10.1039/d2dt02629e |
0.8 |
|
2021 |
Bera A, Kabadwal LM, Bera S, Banerjee D. Recent advances on non-precious metal-catalyzed C-H functionalization of -heteroarenes. Chemical Communications (Cambridge, England). PMID 34874036 DOI: 10.1039/d1cc05899a |
0.795 |
|
2021 |
Bera A, Bera S, Banerjee D. Recent advances in the synthesis of N-heteroarenes catalytic dehydrogenation of N-heterocycles. Chemical Communications (Cambridge, England). PMID 34781335 DOI: 10.1039/d1cc04919d |
0.799 |
|
2021 |
Shadab, Dey G, Sk M, Banerjee D, Aijaz A. Heterogenizing a Homogeneous Nickel Catalyst Using Nanoconfined Strategy for Selective Synthesis of Mono- and 1,2-Disubstituted Benzimidazoles. Inorganic Chemistry. PMID 34652151 DOI: 10.1021/acs.inorgchem.1c02017 |
0.769 |
|
2021 |
Bera S, Kabadwal LM, Banerjee D. Recent advances in transition metal-catalyzed (1,) annulation using (de)-hydrogenative coupling with alcohols. Chemical Communications (Cambridge, England). PMID 34486592 DOI: 10.1039/d1cc03404a |
0.847 |
|
2020 |
Bera S, Bera A, Banerjee D. Nickel-Catalyzed Dehydrogenation of N-Heterocycles Using Molecular Oxygen. Organic Letters. PMID 32806133 DOI: 10.1021/Acs.Orglett.0C02271 |
0.814 |
|
2020 |
Bera S, Bera A, Banerjee D. Nickel-catalyzed hydrogen-borrowing strategy: chemo-selective alkylation of nitriles with alcohols. Chemical Communications (Cambridge, England). PMID 32432612 DOI: 10.1039/D0Cc02261F |
0.856 |
|
2020 |
Sk M, Kumar A, Das J, Banerjee D. A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols. Molecules (Basel, Switzerland). 25. PMID 32235642 DOI: 10.3390/Molecules25071590 |
0.855 |
|
2020 |
Kabadwal LM, Bera S, Banerjee D. Iron-catalysed alkylation of 2-methyl and 4-methyl azaarenes with alcohols via C-H bond activation. Chemical Communications (Cambridge, England). PMID 32227001 DOI: 10.1039/D0Cc01593H |
0.817 |
|
2019 |
Alanthadka A, Bera S, Vellakkaran M, Banerjee D. Nickel-Catalyzed Double Dehydrogenative Coupling of Secondary Alcohols and β-Amino Alcohols to Access Substituted Pyrroles. The Journal of Organic Chemistry. PMID 31532669 DOI: 10.1021/Acs.Joc.9B01819 |
0.851 |
|
2019 |
Das J, Vellakkaran M, Sk M, Banerjee D. Iron-Catalyzed Coupling of Methyl -Heteroarenes with Primary Alcohols: Direct Access to -Selective Olefins. Organic Letters. PMID 31469574 DOI: 10.1021/Acs.Orglett.9B02793 |
0.837 |
|
2019 |
Alanthadka A, Bera S, Banerjee D. Iron-Catalyzed Ligand Free α-Alkylation of Methylene Ketones and β-Alkylation of Secondary Alcohols Using Primary Alcohols. The Journal of Organic Chemistry. PMID 31398035 DOI: 10.1021/Acs.Joc.9B01600 |
0.836 |
|
2019 |
Das J, Vellakkaran M, Banerjee D. Nickel-catalysed direct α-olefination of alkyl substituted N-heteroarenes with alcohols. Chemical Communications (Cambridge, England). PMID 31187810 DOI: 10.1039/C9Cc03591E |
0.847 |
|
2019 |
Bera A, Sk M, Singh K, Banerjee D. Nickel-catalysed dehydrogenative coupling of aromatic diamines with alcohols: selective synthesis of substituted benzimidazoles and quinoxalines. Chemical Communications (Cambridge, England). PMID 31050346 DOI: 10.1039/C9Cc02319D |
0.851 |
|
2018 |
Das J, Vellakkaran M, Banerjee D. Nickel-Catalyzed Alkylation of Ketone Enolates: Synthesis of Mono-Selective Linear Ketones. The Journal of Organic Chemistry. PMID 30548070 DOI: 10.1021/Acs.Joc.8B02609 |
0.859 |
|
2018 |
Singh K, Kabadwal LM, Bera S, Alanthadka A, Banerjee D. Nickel-Catalyzed Synthesis of N-substituted Pyrroles using Diols with Aryl and Alkyl Amines. The Journal of Organic Chemistry. PMID 30474975 DOI: 10.1021/Acs.Joc.8B02666 |
0.846 |
|
2018 |
Kabadwal LM, Das J, Banerjee D. Mn(ii)-catalysed alkylation of methylene ketones with alcohols: direct access to functionalised branched products. Chemical Communications (Cambridge, England). PMID 30403235 DOI: 10.1039/C8Cc08010K |
0.839 |
|
2018 |
Vellakkaran M, Das J, Bera S, Banerjee D. Nickel-catalysed alkylation of C(sp)-H bonds with alcohols: direct access to functionalised N-heteroaromatics. Chemical Communications (Cambridge, England). PMID 30327805 DOI: 10.1039/C8Cc06370B |
0.823 |
|
2018 |
Das J, Singh K, Vellakkaran M, Banerjee D. Nickel-Catalyzed Hydrogen-Borrowing Strategy for α-Alkylation of Ketones with Alcohols: A New Route to Branched gem-Bis(alkyl) Ketones. Organic Letters. PMID 30203978 DOI: 10.1021/Acs.Orglett.8B02256 |
0.856 |
|
2018 |
Das J, Banerjee D. Nickel Catalyzed Phosphine Free Direct N-alkylation of Amides with Alcohols. The Journal of Organic Chemistry. PMID 29441778 DOI: 10.1021/Acs.Joc.7B03215 |
0.86 |
|
2018 |
Singh K, Vellakkaran M, Banerjee D. A nitrogen-ligated nickel-catalyst enables selective intermolecular cyclisation of β- and γ-amino alcohols with ketones: access to five and six-membered N-heterocycles Green Chemistry. 20: 2250-2256. DOI: 10.1039/C8Gc00318A |
0.845 |
|
2017 |
Banerjee D, Junge K, Beller M. Corrigendum: A General Catalytic Hydroamidation of 1,3-Dienes: Atom-Efficient Synthesis of N-Allyl Heterocycles, Amides, and Sulfonamides. Angewandte Chemie (International Ed. in English). 56: 16436-16438. PMID 29265739 DOI: 10.1002/Anie.201710801 |
0.575 |
|
2017 |
Vellakkaran M, Singh K, Banerjee D. An Efficient and Selective Nickel-Catalyzed Direct N-Alkylation of Anilines with Alcohols Acs Catalysis. 7: 8152-8158. DOI: 10.1021/Acscatal.7B02817 |
0.861 |
|
2015 |
Mazuela J, Banerjee D, Bäckvall JE. Palladium(II)-Catalyzed Tandem Oxidative Acetoxylation/ortho C-H Activation/Carbocyclization of Arylallenes. Journal of the American Chemical Society. 137: 9559-62. PMID 26201012 DOI: 10.1021/Jacs.5B06068 |
0.53 |
|
2015 |
Jagadeesh RV, Banerjee D, Arockiam PB, Junge H, Junge K, Pohl MM, Radnik J, Brückner A, Beller M. Highly selective transfer hydrogenation of functionalised nitroarenes using cobalt-based nanocatalysts Green Chemistry. 17: 898-902. DOI: 10.1039/C4Gc00731J |
0.698 |
|
2014 |
Banerjee D, Junge K, Beller M. Cooperative catalysis by palladium and a chiral phosphoric acid: enantioselective amination of racemic allylic alcohols. Angewandte Chemie (International Ed. in English). 53: 13049-53. PMID 25303227 DOI: 10.1002/Anie.201405511 |
0.625 |
|
2014 |
Banerjee D, Jagadeesh RV, Junge K, Pohl MM, Radnik J, Brückner A, Beller M. Convenient and mild epoxidation of alkenes using heterogeneous cobalt oxide catalysts. Angewandte Chemie (International Ed. in English). 53: 4359-63. PMID 24644140 DOI: 10.1002/Anie.201310420 |
0.514 |
|
2014 |
Banerjee D, Junge K, Beller M. A general catalytic hydroamidation of 1,3-dienes: atom-efficient synthesis of N-allyl heterocycles, amides, and sulfonamides. Angewandte Chemie (International Ed. in English). 53: 1630-5. PMID 24452993 DOI: 10.1002/anie.201308874 |
0.575 |
|
2014 |
Banerjee D, Junge K, Beller M. Palladium-catalysed regioselective hydroamination of 1,3-dienes: Synthesis of allylic amines Organic Chemistry Frontiers. 1: 368-372. DOI: 10.1039/C4Qo00023D |
0.604 |
|
2012 |
Banerjee D, Jagadeesh RV, Junge K, Junge H, Beller M. Efficient and convenient palladium-catalyzed amination of allylic alcohols with N-heterocycles. Angewandte Chemie (International Ed. in English). 51: 11556-60. PMID 23023833 DOI: 10.1002/Anie.201206319 |
0.769 |
|
2012 |
Banerjee D, Jagadeesh RV, Junge K, Junge H, Beller M. An efficient and convenient palladium catalyst system for the synthesis of amines from allylic alcohols. Chemsuschem. 5: 2039-44. PMID 22893300 DOI: 10.1002/Cssc.201200247 |
0.784 |
|
2010 |
Rao MLN, Banerjee D, Dhanorkar RJ. Pd-catalyzed coupling of aryl iodides with triarylbismuths as atom-economic multi-coupling organometallic nucleophiles under mild conditions Tetrahedron Letters. 51: 6101-6104. DOI: 10.1016/J.Tetlet.2010.09.053 |
0.818 |
|
2010 |
Rao MLN, Awasthi DK, Banerjee D. An expeditious and convergent synthesis of ailanthoidol Tetrahedron Letters. 51: 1979-1981. DOI: 10.1016/J.Tetlet.2010.02.018 |
0.798 |
|
2010 |
Rao MLN, Banerjee D, Dhanorkar RJ. Pd(0)-catalyzed couplings using bromide and chloride derivatives of Baylis-Hillman adducts with triarylbismuths as atom-efficient multi-coupling nucleophiles Tetrahedron. 66: 3623-3632. DOI: 10.1016/J.Tet.2010.03.020 |
0.827 |
|
2010 |
Rao MLN, Banerjee D, Giri S. Palladium-catalyzed cross-couplings of allylic carbonates with triarylbismuths as multi-coupling atom-efficient organometallic nucleophiles Journal of Organometallic Chemistry. 695: 1518-1525. DOI: 10.1016/J.Jorganchem.2010.03.010 |
0.811 |
|
2009 |
Rao MLN, Banerjee D, Giri S. Arylations of allylic acetates with triarylbismuths as atom-efficient multi-coupling reagents under palladium catalysis Tetrahedron Letters. 50: 5757-5761. DOI: 10.1016/J.Tetlet.2009.07.148 |
0.831 |
|
2008 |
Rao MLN, Jadhav DN, Banerjee D. A new palladium catalyzed protocol for atom-efficient cross-coupling reactions of triarylbismuths with aryl halides and triflates Tetrahedron. 64: 5762-5772. DOI: 10.1016/J.Tet.2008.04.011 |
0.804 |
|
2007 |
Rao MLN, Banerjee D, Jadhav DN. Palladium catalyzed atom-efficient cross-coupling reactions of triarylbismuths with aryl iodides and aryl triflates Tetrahedron Letters. 48: 6644-6647. DOI: 10.1016/J.Tetlet.2007.07.107 |
0.798 |
|
2007 |
Rao MLN, Banerjee D, Jadhav DN. Palladium catalyzed atom-efficient cross-coupling reactions of triarylbismuths with aryl bromides Tetrahedron Letters. 48: 2707-2711. DOI: 10.1016/J.Tetlet.2007.02.068 |
0.795 |
|
2007 |
Rao MLN, Awasthi DK, Banerjee D. Microwave-mediated solvent free Rap-Stoermer reaction for efficient synthesis of benzofurans Tetrahedron Letters. 48: 431-434. DOI: 10.1016/J.Tetlet.2006.11.077 |
0.799 |
|
2007 |
Rao MLN, Venkatesh V, Banerjee D. Atom-efficient cross-coupling reactions of triarylbismuths with acyl chlorides under Pd(0) catalysis Tetrahedron. 63: 12917-12926. DOI: 10.1016/J.Tet.2007.10.047 |
0.465 |
|
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