| Year |
Citation |
Score |
| 2024 |
Liu C, Ge R, Chen J, Guo H, Bartholome TA, Maiti D, Ge H. Facile construction of distal and diversified tertiary and quaternary stereocenters. Proceedings of the National Academy of Sciences of the United States of America. 121: e2408541121. PMID 39665763 DOI: 10.1073/pnas.2408541121 |
0.597 |
|
| 2024 |
Pradhan S, Dutta U, Biswas JP, Elsaid M, Ge H, Maiti D. Palladium-Catalyzed -Selective Arylation of 1-Naphthamide. Organic Letters. 26: 10946-10950. PMID 39648741 DOI: 10.1021/acs.orglett.4c04104 |
0.863 |
|
| 2024 |
Mandal A, Biswas JP, Maiti D. Rhodium-Catalyzed Meta-C-H Arylation of Arenes with Varied Linker Lengths: Bridging Catalytic Selectivity with Structural Diversity. Angewandte Chemie (International Ed. in English). e202419954. PMID 39563025 DOI: 10.1002/anie.202419954 |
0.747 |
|
| 2024 |
Ghosh P, Maiti S, Malandain A, Raja D, Loreau O, Maity B, Roy TK, Audisio D, Maiti D. Taming CO via Synergistic Triple Catalysis in Anti-Markovnikov Hydrocarboxylation of Alkenes. Journal of the American Chemical Society. PMID 39468468 DOI: 10.1021/jacs.4c12294 |
0.31 |
|
| 2024 |
Maji S, Rawal P, Ghosh A, Pidiyar K, Al-Thabaiti SA, Gupta P, Maiti D. Metal-free Borylation of α-Naphthamides and Phenylacetic Acid Drug. Jacs Au. 4: 3679-3689. PMID 39328765 DOI: 10.1021/jacsau.4c00660 |
0.652 |
|
| 2024 |
Pradhan S, Maiti S, Dutta S, Russell CA, Tyagi S, Maiti D. A Modular Approach for Accessing 3D Heterocycles via 1,2-Dicyanation of Planar N-Heteroarenes. Angewandte Chemie (International Ed. in English). e202412979. PMID 39283171 DOI: 10.1002/anie.202412979 |
0.61 |
|
| 2024 |
Dutta B, Mahajan M, Ghosh A, Dajek M, Kowalczyk R, Mondal B, Ge H, Maiti D. Hydrogen bonding template enables remote meta-C-H alkenylation of nitroarenes with electron-deficient alkenes. Nature Communications. 15: 7543. PMID 39215005 DOI: 10.1038/s41467-024-51764-1 |
0.784 |
|
| 2024 |
Ali W, Oliver GA, Werz DB, Maiti D. Pd-catalyzed regioselective activation of C(sp)-H and C(sp)-H bonds. Chemical Society Reviews. PMID 39212454 DOI: 10.1039/d4cs00408f |
0.652 |
|
| 2024 |
Werz DB, Teja C, Kolb S, Colonna P, Grover J, Lahiri GK, Pieters G, Maiti D, Garcia-Argote S. Deuteration and Tritiation of Pharmaceuticals by Non-Directed Palladium-Catalyzed C-H Activation in Heavy and Super-Heavy Water. Angewandte Chemie (International Ed. in English). e202410162. PMID 39109510 DOI: 10.1002/anie.202410162 |
0.59 |
|
| 2024 |
Maiti D, Sebastian AT, Maji S, Rajashekhar M, Maiti S, Kowalczyk R. Palladium-Catalyzed Remote C-H Functionalization: Non-Covalent Interactions and Reversibly Bound Templates. Angewandte Chemie (International Ed. in English). e202410806. PMID 39072955 DOI: 10.1002/anie.202410806 |
0.391 |
|
| 2024 |
Pal T, Ghosh P, Islam M, Guin S, Maji S, Dutta S, Das J, Ge H, Maiti D. Tandem dehydrogenation-olefination-decarboxylation of cycloalkyl carboxylic acids via multifold C-H activation. Nature Communications. 15: 5370. PMID 38918374 DOI: 10.1038/s41467-024-49359-x |
0.851 |
|
| 2023 |
Saha A, Ali W, Werz DB, Maiti D. Highly scalable photoinduced synthesis of silanols via untraversed pathway for chlorine radical (Cl) generation. Nature Communications. 14: 8173. PMID 38071374 DOI: 10.1038/s41467-023-43286-z |
0.724 |
|
| 2023 |
Sivaraj C, Maiti D, Gandhi T. Photo-Catalyzed Acyl Azolium Promoted Selective α-C(sp3)-H Acylation of Acetone via HAT: Access to Thermodynamically Less Favoured (Z)-α,β-Unsaturated Ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). e202303626. PMID 37997552 DOI: 10.1002/chem.202303626 |
0.355 |
|
| 2023 |
Azad SA, Bera A, Samanta J, Sepay N, Jana R, Pal CK, Molla MR, Maiti D, Samanta S. Urea Promoted Neat Synthesis of Fused Dihydroisoquinolines and Disubstituted Pyridines: A Mechanistic Observation with Molecular Sensing Studies. Chemistry (Weinheim An Der Bergstrasse, Germany). e202303287. PMID 37997510 DOI: 10.1002/chem.202303287 |
0.308 |
|
| 2023 |
Bhattacharya T, Ghosh S, Dutta S, Guin S, Ghosh A, Ge H, Sunoj RB, Maiti D. Combinatorial Ligand Assisted Simultaneous Control of Axial and Central Chirality in Highly Stereoselective C-H Allylation. Angewandte Chemie (International Ed. in English). e202310112. PMID 37997014 DOI: 10.1002/anie.202310112 |
0.82 |
|
| 2023 |
Guria S, Dolui D, Das C, Ghorai S, Vishal V, Maiti D, Lahiri GK, Dutta A. Energy-efficient CO/CO interconversion by homogeneous copper-based molecular catalysts. Nature Communications. 14: 6859. PMID 37891216 DOI: 10.1038/s41467-023-42638-z |
0.492 |
|
| 2023 |
Dutta U, Prakash G, Devi K, Borah K, Zhang X, Maiti D. Directing group assisted -selective C-H alkynylation of unbiased arenes enabled by rhodium catalysis. Chemical Science. 14: 11381-11388. PMID 37886091 DOI: 10.1039/d3sc03528j |
0.839 |
|
| 2023 |
Saha A, Sen C, Guin S, Das C, Maiti D, Sen S, Maiti D. Photoinduced [3+2] Cycloaddition of Carbenes and Nitriles: A Versatile Approach to Oxazole Synthesis. Angewandte Chemie (International Ed. in English). e202308916. PMID 37843822 DOI: 10.1002/anie.202308916 |
0.772 |
|
| 2023 |
Sinha SK, Ghosh P, Jain S, Maiti S, Al-Thabati SA, Alshehri AA, Mokhtar M, Maiti D. Transition-metal catalyzed C-H activation as a means of synthesizing complex natural products. Chemical Society Reviews. PMID 37811747 DOI: 10.1039/d3cs00282a |
0.687 |
|
| 2023 |
Grover J, Maji S, Teja C, Al Thabaiti SA, Mostafa MMM, Lahiri GK, Maiti D. Base Metal Catalyst for Indirect Hydrogenation of CO. Acs Organic & Inorganic Au. 3: 299-304. PMID 37810409 DOI: 10.1021/acsorginorgau.3c00023 |
0.513 |
|
| 2023 |
Das J, Ali W, Ghosh A, Pal T, Mandal A, Teja C, Dutta S, Pothikumar R, Ge H, Zhang X, Maiti D. Access to unsaturated bicyclic lactones by overriding conventional C(sp)-H site selectivity. Nature Chemistry. PMID 37563324 DOI: 10.1038/s41557-023-01295-x |
0.861 |
|
| 2023 |
Mittal AK, Pathak P, Prakash G, Maiti D. Highly scalable and inherently safer preparation of di, tri and tetra nitrate esters using continuous flow chemistry. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301662. PMID 37505482 DOI: 10.1002/chem.202301662 |
0.485 |
|
| 2023 |
Bhattacharya T, Baroliya PK, Al-Thabaiti SA, Maiti D. Simplifying the Synthesis of Nonproteinogenic Amino Acids via Palladium-Catalyzed δ-Methyl C-H Olefination of Aliphatic Amines and Amino Acids. Jacs Au. 3: 1975-1983. PMID 37502162 DOI: 10.1021/jacsau.3c00215 |
0.678 |
|
| 2023 |
Ali W, Saha A, Ge H, Maiti D. Photoinduced -Selective C-H Oxygenation of Arenes. Jacs Au. 3: 1790-1799. PMID 37388693 DOI: 10.1021/jacsau.3c00231 |
0.793 |
|
| 2023 |
Maiti D, Saha A, Guin S, Maiti D, Sen S. Unveiling catalyst-free electro-photochemical reactivity of aryl diazoesters and facile synthesis of oxazoles, imide-fused pyrroles and tetrahydro-epoxy-pyridines carbene radical anions. Chemical Science. 14: 6216-6225. PMID 37325143 DOI: 10.1039/d3sc00089c |
0.761 |
|
| 2023 |
Elsaid M, Ge R, Liu C, Maiti D, Ge H. Site-Selective C-H Functionalization of Carbazoles. Angewandte Chemie (International Ed. in English). e202303110. PMID 37186413 DOI: 10.1002/anie.202303110 |
0.703 |
|
| 2023 |
Olding A, Ho CC, Maiti D, Bissember AC. Structural authentication of intermediates of mechanistic significance in palladium- and nickel-catalysed cross-couplings: case studies. Chemical Communications (Cambridge, England). PMID 37039067 DOI: 10.1039/d3cc00882g |
0.308 |
|
| 2023 |
Roy S, Panja S, Sahoo SR, Chatterjee S, Maiti D. Enroute sustainability: metal free C-H bond functionalisation. Chemical Society Reviews. PMID 36924227 DOI: 10.1039/d0cs01466d |
0.378 |
|
| 2023 |
Baroliya PK, Dhaker M, Panja S, Al-Thabaiti SA, Albukhari SM, Alsulami QA, Dutta A, Maiti D. Transition metal catalyzed C-H functionalization through electrocatalysis. Chemsuschem. e202202201. PMID 36881013 DOI: 10.1002/cssc.202202201 |
0.376 |
|
| 2022 |
Mittal AK, Prakash G, Pathak P, Maiti D. Synthesis of picramide using nitration and ammonolysis in continuous flow. Chemistry, An Asian Journal. PMID 36484628 DOI: 10.1002/asia.202201028 |
0.422 |
|
| 2022 |
Panja S, Ahsan S, Pal T, Kolb S, Ali W, Sharma S, Das C, Grover J, Dutta A, Werz DB, Paul A, Maiti D. Non-directed Pd-catalysed electrooxidative olefination of arenes. Chemical Science. 13: 9432-9439. PMID 36093017 DOI: 10.1039/d2sc03288k |
0.591 |
|
| 2022 |
Mandal D, Maji S, Pal T, Sinha SK, Maiti D. Recent advances in transition metal-mediated trifluoromethylation reactions. Chemical Communications (Cambridge, England). 58: 10442-10468. PMID 36069245 DOI: 10.1039/d2cc04082d |
0.663 |
|
| 2022 |
Maiti S, Li Y, Sasmal S, Guin S, Bhattacharya T, Lahiri GK, Paton RS, Maiti D. Author Correction: Expanding chemical space by para-C-H arylation of arenes. Nature Communications. 13: 4980. PMID 36008410 DOI: 10.1038/s41467-022-32720-3 |
0.812 |
|
| 2022 |
Saha A, Ghosh A, Guin S, Panda S, Mal DK, Majumdar A, Akita M, Maiti D. Substrate-Rhodium Cooperativity in Photoinduced ortho-Alkynylation of Arenes. Angewandte Chemie (International Ed. in English). PMID 36000535 DOI: 10.1002/anie.202210492 |
0.824 |
|
| 2022 |
Maiti S, Roy S, Ghosh P, Kasera A, Maiti D. Photo-Excited Nickel-Catalyzed Silyl-Radical-Mediated Direct Activation of Carbamoyl Chlorides To Access (Hetero)aryl Car-bamides. Angewandte Chemie (International Ed. in English). PMID 35929544 DOI: 10.1002/anie.202207472 |
0.339 |
|
| 2022 |
Mandal D, Roychowdhury S, Biswas JP, Maiti S, Maiti D. Transition-metal-catalyzed C-H bond alkylation using olefins: recent advances and mechanistic aspects. Chemical Society Reviews. PMID 35912472 DOI: 10.1039/d1cs00923k |
0.837 |
|
| 2022 |
Maiti S, Li Y, Sasmal S, Guin S, Bhattacharya T, Lahiri GK, Paton RS, Maiti D. Expanding chemical space by para-C-H arylation of arenes. Nature Communications. 13: 3963. PMID 35803905 DOI: 10.1038/s41467-022-31506-x |
0.829 |
|
| 2022 |
Sinha SK, Panja S, Grover J, Hazra PS, Pandit S, Bairagi Y, Zhang X, Maiti D. Dual Ligand Enabled Nondirected C-H Chalcogenation of Arenes and Heteroarenes. Journal of the American Chemical Society. PMID 35759373 DOI: 10.1021/jacs.2c02126 |
0.681 |
|
| 2022 |
Sasmal S, Prakash G, Dutta U, Laskar R, Lahiri GK, Maiti D. Directing group assisted rhodium catalyzed -C-H alkynylation of arenes. Chemical Science. 13: 5616-5621. PMID 35694332 DOI: 10.1039/d2sc00982j |
0.872 |
|
| 2022 |
Yang K, Li Z, Liu C, Li Y, Hu Q, Elsaid M, Li B, Das J, Dang Y, Maiti D, Ge H. Ligand-promoted palladium-catalyzed β-methylene C-H arylation of primary aldehydes. Chemical Science. 13: 5938-5943. PMID 35685787 DOI: 10.1039/d2sc01677j |
0.852 |
|
| 2022 |
Das C, Grover J, Das A, Maiti D, Dutta A, Lahiri GK. Recent developments in first-row transition metal complex-catalyzed CO hydrogenation. Dalton Transactions (Cambridge, England : 2003). PMID 35587113 DOI: 10.1039/d2dt00663d |
0.53 |
|
| 2022 |
Saha A, Guin S, Ali W, Bhattacharya T, Sasmal S, Goswami N, Prakash G, Sinha SK, Chandrashekar HB, Panda S, Anjana SS, Maiti D. Correction to "Photoinduced Regioselective Olefination of Arenes at Proximal and Distal Sites". Journal of the American Chemical Society. PMID 35537037 DOI: 10.1021/jacs.2c04257 |
0.774 |
|
| 2022 |
Dutta S, Bhattacharya T, Geffers FJ, Bürger M, Maiti D, Werz DB. Pd-catalysed C-H functionalisation of free carboxylic acids. Chemical Science. 13: 2551-2573. PMID 35340865 DOI: 10.1039/d1sc05392b |
0.667 |
|
| 2022 |
Prakash G, Paul N, Oliver GA, Werz DB, Maiti D. C-H deuteration of organic compounds and potential drug candidates. Chemical Society Reviews. PMID 35320331 DOI: 10.1039/d0cs01496f |
0.613 |
|
| 2022 |
Grover J, Prakash G, Goswami N, Maiti D. Traditional and sustainable approaches for the construction of C-C bonds by harnessing C-H arylation. Nature Communications. 13: 1085. PMID 35228555 DOI: 10.1038/s41467-022-28707-9 |
0.779 |
|
| 2022 |
Saha A, Guin S, Ali W, Bhattacharya T, Sasmal S, Goswami N, Prakash G, Sinha SK, Chandrashekar HB, Panda S, Anjana SS, Maiti D. Photoinduced Regioselective Olefination of Arenes at Proximal and Distal Sites. Journal of the American Chemical Society. PMID 35050599 DOI: 10.1021/jacs.1c12311 |
0.842 |
|
| 2022 |
Dutta U, Maiti D. Emergence of Pyrimidine-Based -Directing Group: Journey from Weak to Strong Coordination in Diversifying -C-H Functionalization. Accounts of Chemical Research. PMID 35021007 DOI: 10.1021/acs.accounts.1c00629 |
0.825 |
|
| 2021 |
Goswami N, Bhattacharya T, Maiti D. Transient directing ligands for selective metal-catalysed C-H activation. Nature Reviews. Chemistry. 5: 646-659. PMID 37118417 DOI: 10.1038/s41570-021-00311-3 |
0.81 |
|
| 2021 |
Baidya M, Maiti D, Roy L, De Sarkar S. Trifluoroethanol as a Unique Additive for the Chemoselective Electrooxidation of Enamines to Access Unsymmetrically Substituted NH-Pyrroles. Angewandte Chemie (International Ed. in English). PMID 34851544 DOI: 10.1002/anie.202111679 |
0.395 |
|
| 2021 |
Bains AK, Kundu A, Maiti D, Adhikari D. Ligand-redox assisted nickel catalysis toward stereoselective synthesis of (+1)-membered cycloalkanes from 1,-diols with methyl ketones. Chemical Science. 12: 14217-14223. PMID 34760207 DOI: 10.1039/d1sc04261k |
0.31 |
|
| 2021 |
Sinha SK, Roy TK, Modak A, Maiti D. Enabling the Facile Synthesis of Arenes by Transition Metal Catalyzed Decarbonylation Methodology. Chemical Record (New York, N.Y.). PMID 34713555 DOI: 10.1002/tcr.202100244 |
0.796 |
|
| 2021 |
Sahoo SR, Dutta S, Al-Thabaiti SA, Mokhtar M, Maiti D. Transition metal catalyzed C-H bond activation by -metallacycle intermediates. Chemical Communications (Cambridge, England). 57: 11885-11903. PMID 34693418 DOI: 10.1039/d1cc05042g |
0.841 |
|
| 2021 |
Sinha SK, Guin S, Maiti S, Biswas JP, Porey S, Maiti D. Toolbox for Distal C-H Bond Functionalizations in Organic Molecules. Chemical Reviews. PMID 34662117 DOI: 10.1021/acs.chemrev.1c00220 |
0.847 |
|
| 2021 |
Halder A, Mahanty K, Maiti D, De Sarkar S. Highly Diastereoselective Synthesis of Dihydro-benzoimidazo-[1,3]-thiazines via Electro-oxidative Selenocyclization of Thioallyl Benzoimidazoles. Chemistry, An Asian Journal. PMID 34609085 DOI: 10.1002/asia.202101033 |
0.335 |
|
| 2021 |
Paul N, Maity S, Panja S, Maiti D. Recent Advances in the Nitration of Olefins. Chemical Record (New York, N.Y.). PMID 34569706 DOI: 10.1002/tcr.202100217 |
0.759 |
|
| 2021 |
Ali W, Prakash G, Maiti D. Recent development in transition metal-catalysed C-H olefination. Chemical Science. 12: 2735-2759. PMID 34164039 DOI: 10.1039/d0sc05555g |
0.768 |
|
| 2021 |
Ali W, Prakash G, Maiti D. Recent development in transition metal-catalysed C-H olefination. Chemical Science. 12: 2735-2759. PMID 34164039 DOI: 10.1039/d0sc05555g |
0.768 |
|
| 2021 |
Bhattacharya T, Ghosh A, Maiti D. Hexafluoroisopropanol: the magical solvent for Pd-catalyzed C-H activation. Chemical Science. 12: 3857-3870. PMID 34163654 DOI: 10.1039/d0sc06937j |
0.845 |
|
| 2021 |
Bhattacharya T, Ghosh A, Maiti D. Hexafluoroisopropanol: the magical solvent for Pd-catalyzed C-H activation. Chemical Science. 12: 3857-3870. PMID 34163654 DOI: 10.1039/d0sc06937j |
0.845 |
|
| 2021 |
Chandrashekar HB, Dolui P, Li B, Mandal A, Liu H, Guin S, Ge H, Maiti D. Ligand Enabled δ-C(sp3)-H Borylation of Aliphatic Amines. Angewandte Chemie (International Ed. in English). PMID 34117691 DOI: 10.1002/anie.202105204 |
0.845 |
|
| 2021 |
Murali K, Machado LA, Carvalho RL, Pedrosa LF, Mukherjee R, Silva Júnior END, Maiti D. Decoding directing groups and their pivotal role in C-H activation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34038596 DOI: 10.1002/chem.202101004 |
0.446 |
|
| 2021 |
Dutta U, Maiti S, Bhattacharya T, Maiti D. Arene diversification through distal C(sp)-H functionalization. Science (New York, N.Y.). 372. PMID 33986152 DOI: 10.1126/science.abd5992 |
0.855 |
|
| 2021 |
Basak S, Dutta S, Maiti D. Accessing C2-Functionalized 1,3-(Benz)azolesthrough Transition Metal-Catalyzed C-H Activation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33909304 DOI: 10.1002/chem.202100475 |
0.842 |
|
| 2021 |
Mokhtar M, Alzhrani G, Aazam ES, Saleh TS, Al-Faifi S, Panja S, Maiti D. Synergistic Effect of NiLDH@YZ Hybrid and Mechanochemical Agitation on Glaser Homocoupling Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33848016 DOI: 10.1002/chem.202100018 |
0.317 |
|
| 2021 |
Biswas JP, Ansari M, Paik A, Sasmal S, Paul S, Rana S, Rajaraman G, Maiti D. Effect of ligand backbone on the reactivity and mechanistic paradigm of non-heme iron(IV)-oxo during olefin epoxidation. Angewandte Chemie (International Ed. in English). PMID 33836110 DOI: 10.1002/anie.202102484 |
0.797 |
|
| 2021 |
Nale SD, Maiti D, Lee YR. Construction of Highly Functionalized Xanthones via Rh-Catalyzed Cascade C-H Activation/-Annulation. Organic Letters. PMID 33719464 DOI: 10.1021/acs.orglett.1c00391 |
0.661 |
|
| 2021 |
Bag S, Jana S, Pradhan S, Bhowmick S, Goswami N, Sinha SK, Maiti D. Imine as a linchpin approach for meta-C-H functionalization. Nature Communications. 12: 1393. PMID 33654108 DOI: 10.1038/s41467-021-21633-2 |
0.858 |
|
| 2021 |
Pimparkar S, Koodan A, Maiti S, Ahmed NS, Mostafa MMM, Maiti D. C-CN bond formation: an overview of diverse strategies. Chemical Communications (Cambridge, England). PMID 33587061 DOI: 10.1039/d0cc07783f |
0.818 |
|
| 2021 |
Rana S, Biswas JP, Paul S, Paik A, Maiti D. Organic synthesis with the most abundant transition metal-iron: from rust to multitasking catalysts. Chemical Society Reviews. PMID 33399140 DOI: 10.1039/d0cs00688b |
0.84 |
|
| 2021 |
Carvalho RL, Almeida RG, Murali K, Machado LA, Pedrosa LF, Dolui P, Maiti D, da Silva Júnior EN. Removal and modification of directing groups used in metal-catalyzed C-H functionalization: the magical step of conversion into 'conventional' functional groups. Organic & Biomolecular Chemistry. PMID 33393535 DOI: 10.1039/d0ob02232b |
0.834 |
|
| 2020 |
Das J, Guin S, Maiti D. Diverse strategies for transition metal catalyzed distal C(sp)-H functionalizations. Chemical Science. 11: 10887-10909. PMID 34094339 DOI: 10.1039/d0sc04676k |
0.852 |
|
| 2020 |
Das J, Dolui P, Ali W, Biswas JP, Chandrashekar HB, Prakash G, Maiti D. A direct route to six and seven membered lactones γ-C(sp)-H activation: a simple protocol to build molecular complexity. Chemical Science. 11: 9697-9702. PMID 34094235 DOI: 10.1039/d0sc03144e |
0.855 |
|
| 2020 |
Maiti D, Dutta U, Porey S, Pimparkar S, Mandal A, Grover J, Koodan A. Para-Selective Arylation of Arenes: A Direct Route to Biaryls by Norbornene Relay Palladation. Angewandte Chemie (International Ed. in English). PMID 32754958 DOI: 10.1002/Anie.202005664 |
0.862 |
|
| 2020 |
Maiti D, Baccalini A, Faita G, Zanoni G. Transition Metal Promoted Cascade Heterocycles Synthesis via C-H Functionalization. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32557863 DOI: 10.1002/Chem.202001832 |
0.511 |
|
| 2020 |
Bag S, K S, Mondal A, Jayarajan R, Dutta U, Porey S, Sunoj RB, Maiti D. Palladium-catalyzed -C-H allylation of arenes: A unique combination of pyrimidine-based template and hexafluoroisopropanol. Journal of the American Chemical Society. PMID 32496791 DOI: 10.1021/Jacs.0C05223 |
0.867 |
|
| 2020 |
Casali E, Kalra P, Brochetta M, Borsari T, Gandini A, Patra T, Zanoni G, Maiti D. Overriding ortho selectivity by template assisted meta-C-H activation of benzophenones. Chemical Communications (Cambridge, England). PMID 32478359 DOI: 10.1039/D0Cc03172K |
0.799 |
|
| 2020 |
Sasmal S, Sinha SK, Lahiri GK, Maiti D. A directing group-assisted ruthenium-catalyzed approach to access meta-nitrated phenols. Chemical Communications (Cambridge, England). PMID 32458947 DOI: 10.1039/D0Cc02851G |
0.778 |
|
| 2020 |
Jayarajan R, Chandrashekar HB, Dalvi AK, Maiti D. Ultrasound-facilitated direct meta-C-H functionalization of arene: A time economical strategy under ambient temperature with improved yield and selectivity. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32289187 DOI: 10.1002/Chem.202001757 |
0.855 |
|
| 2020 |
Pimparkar S, Bhattacharya T, Maji A, Saha A, Jayarajan R, Dutta U, Lu G, Lupton DW, Maiti D. Para-Selective Cyanation of Arenes by H-Bonded Template. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32196777 DOI: 10.1002/Chem.202001368 |
0.834 |
|
| 2020 |
Halder A, Maiti D, De Sarkar S. Mechanochemical Synthesis of Functionalized Quinolines by Iodine Mediated Oxidative Annulation. Chemistry, An Asian Journal. PMID 32011806 DOI: 10.1002/asia.201901758 |
0.325 |
|
| 2020 |
Mahanty K, Maiti D, De Sarkar S. Regioselective C-H Sulfonylation of 2-Indazoles by Electrosynthesis. The Journal of Organic Chemistry. PMID 32003566 DOI: 10.1021/acs.joc.9b03330 |
0.386 |
|
| 2020 |
Porey S, Zhang X, Bhowmick S, Kumar Singh V, Guin S, Paton RS, Maiti D. An Alkyne Linchpin Strategy for Drug:Pharmacophore Conjugation: Experimental and Computational Realization of a -selective Inverse Sonogashira Coupling. Journal of the American Chemical Society. PMID 31910623 DOI: 10.1021/Jacs.9B10646 |
0.859 |
|
| 2020 |
Sasmal S, Dutta U, Lahiri GK, Maiti D. Transition Metals and Transition Metals/Lewis Acid Cooperative Catalysis for Directing Group Assisted para-C−H Functionalization Chemistry Letters. DOI: 10.1246/Cl.200500 |
0.784 |
|
| 2020 |
Das J, Dolui P, Ali W, Biswas JP, Chandrashekar HB, Prakash G, Maiti D. A direct route to six and seven membered lactones via γ-C(sp3)–H activation: a simple protocol to build molecular complexity Chemical Science. 11: 9697-9702. DOI: 10.1039/D0Sc03144E |
0.839 |
|
| 2020 |
Coin G, Patra R, Rana S, Biswas JP, Dubourdeaux P, Clémancey M, Visser SPd, Maiti D, Maldivi P, Latour J. Fe-Catalyzed Aziridination Is Governed by the Electron Affinity of the Active Imido-Iron Species Acs Catalysis. 10: 10010-10020. DOI: 10.1021/Acscatal.0C01427 |
0.772 |
|
| 2020 |
Gholap A, Bag S, Pradhan S, Kapdi AR, Maiti D. Diverse meta-C–H Functionalization of Amides Acs Catalysis. 10: 5347-5352. DOI: 10.1021/Acscatal.0C01306 |
0.806 |
|
| 2020 |
Maiti D, Ghosh P, Mondal B. This special edition of the Inorganica Chimica Acta celebrates the outstanding contributions that Prof. G. K. Lahiri has made to the fields of electron transfer research and catalysis based on transition metal complexes. On the occasion of his 60th birthday, the contributions from his former students, colleagues, friends and well-wishers are brought together in this special issue Inorganica Chimica Acta. 509: 119635. DOI: 10.1016/J.Ica.2020.119635 |
0.695 |
|
| 2020 |
Biswas JP, Guin S, Maiti D. Highvalent 3d metal-oxo mediated C–H halogenation: Biomimetic approaches Coordination Chemistry Reviews. 408: 213174. DOI: 10.1016/J.Ccr.2019.213174 |
0.801 |
|
| 2020 |
Goswami N, Maiti D. An Update on Distal C(
sp
3
)−H Functionalization Involving 1,5‐HAT Emerging from Nitrogen Radicals Israel Journal of Chemistry. 60: 303-312. DOI: 10.1002/Ijch.201900172 |
0.656 |
|
| 2020 |
Pal T, Lahiri GK, Maiti D. Copper in Efficient Synthesis of Aromatic Heterocycles with Single Heteroatom European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.202000688 |
0.555 |
|
| 2020 |
Baccalini A, Faita G, Zanoni G, Maiti D. Frontispiece: Transition Metal Promoted Cascade Heterocycle Synthesis through C−H Functionalization Chemistry: a European Journal. 26. DOI: 10.1002/Chem.202084464 |
0.343 |
|
| 2019 |
Baccalini A, Vergura S, Dolui P, Zanoni G, Maiti D. Recent advances in cobalt-catalysed C-H functionalizations. Organic & Biomolecular Chemistry. PMID 31746910 DOI: 10.1039/C9Ob01994D |
0.845 |
|
| 2019 |
Baccalini A, Vergura S, Dolui P, Maiti S, Dutta S, Maity S, Khan FF, Lahiri GK, Zanoni G, Maiti D. Cobalt-Catalyzed C(sp)-H Allylation of Biphenyl Amines with Unbiased Terminal Olefins. Organic Letters. PMID 31638402 DOI: 10.1021/Acs.Orglett.9B03484 |
0.869 |
|
| 2019 |
Dutta U, Maiti S, Pimparkar S, Maiti S, Gahan LR, Krenske EH, Lupton DW, Maiti D. Rhodium catalyzed template-assisted distal -C-H olefination. Chemical Science. 10: 7426-7432. PMID 31489165 DOI: 10.1039/C9Sc01824G |
0.86 |
|
| 2019 |
Cho EJ, Iqbal N, Iqbal N, Maiti D. Access to Multi-Functionalized Benzofurans through Aryl-Nickelation of Alkynes: Efficient Synthesis of Anti-Arrhythmic Drug Amiodarone. Angewandte Chemie (International Ed. in English). PMID 31441180 DOI: 10.1002/Anie.201909015 |
0.567 |
|
| 2019 |
Dolui P, Das J, Chandrashekar HB, Anjana SS, Maiti D. Ligand-Enabled Pd(II)-Catalyzed Iterative γ-C(sp3)-H Arylation of Free Aliphatic Acid. Angewandte Chemie (International Ed. in English). PMID 31353817 DOI: 10.1002/Anie.201907262 |
0.864 |
|
| 2019 |
Kankanala R, Biswas JP, Jana S, Achar TK, Porey S, Maiti D. Co-ordination assisted distal C-H alkylation of fused heterocycles. Angewandte Chemie (International Ed. in English). PMID 31336005 DOI: 10.1002/Anie.201907544 |
0.845 |
|
| 2019 |
Brochetta M, Borsari T, Bag S, Jana S, Maiti S, Porta A, Werz DB, Zanoni G, Maiti D. Direct meta-C-H Perfluoroalkenylation of Arenes Enabled by a Cleavable Pyrimidine-Based Template. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31215707 DOI: 10.1002/Chem.201902811 |
0.866 |
|
| 2019 |
Agasti S, Pal T, Achar TK, Maiti S, Pal D, Mandal S, Daud K, Lahiri GK, Maiti D. Regioselective Synthesis of Fused Furans via Decarboxylative Annulation of α,β-Alkenyl Carboxylic Acid with Cyclic Ketone: Synthesis of Biheteroaryl Derivatives. Angewandte Chemie (International Ed. in English). PMID 31162769 DOI: 10.1002/Anie.201906264 |
0.821 |
|
| 2019 |
Achar TK, Zhang X, Mondal R, S SM, Maiti S, Maity S, Pal N, Paton RS, Maiti D. Palladium-Catalyzed Directed meta-Selective C-H Allylation of Arenes: Unactivated Internal Olefins as Allyl Surrogates. Angewandte Chemie (International Ed. in English). PMID 31125484 DOI: 10.1002/Anie.201904608 |
0.847 |
|
| 2019 |
Achar TK, Biswas JP, Porey S, Pal T, Ramakrishna K, Maiti S, Maiti D. Palladium catalyzed template directed C-5 selective olefination of thiazoles. The Journal of Organic Chemistry. PMID 31120754 DOI: 10.1021/Acs.Joc.9B01074 |
0.836 |
|
| 2019 |
Chandrashekar HB, Maji A, Halder G, Banerjee S, Bhattacharyya S, Maiti D. Photocatalyzed borylation using water-soluble quantum dots. Chemical Communications (Cambridge, England). PMID 31073563 DOI: 10.1039/C9Cc01737B |
0.775 |
|
| 2019 |
Bag S, Petzold M, Sur A, Bhowmick S, Werz D, Maiti D. Palladium-Catalyzed Selective meta-C-H Deuteration of Arenes: Reaction Design and Applications. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30977181 DOI: 10.1002/Chem.201901317 |
0.832 |
|
| 2019 |
Maiti D, Paton RS, Guin S, Dolui P, Zhang X, Paul S, Singh VK, Pradhan S, Chandrashekar HB, S AS. Iterative Arylation of Amino Acids and Aliphatic Amines via δ-C(sp3)-H Activation: Experimental and Computational Exploration. Angewandte Chemie (International Ed. in English). PMID 30821038 DOI: 10.1002/Anie.201900479 |
0.842 |
|
| 2019 |
Sinha SK, Bhattacharya T, Maiti D. Correction: Role of hexafluoroisopropanol in C–H activation Reaction Chemistry & Engineering. 4: 1492-1492. DOI: 10.1039/C9Re90036E |
0.542 |
|
| 2019 |
Jayarajan R, Kumar R, Gupta J, Dev G, Kadu P, Chatterjee D, Bahadur D, Maiti D, Maji SK. Fabrication of an amyloid fibril-palladium nanocomposite: a sustainable catalyst for C–H activation and the electrooxidation of ethanol Journal of Materials Chemistry A. 7: 4486-4493. DOI: 10.1039/C8Ta11134K |
0.654 |
|
| 2019 |
Sinha SK, Bhattacharya T, Maiti D. Role of hexafluoroisopropanol in C–H activation Reaction Chemistry & Engineering. 4: 244-253. DOI: 10.1039/C8Re00225H |
0.664 |
|
| 2019 |
Agasti S, Mondal B, Achar TK, Sinha SK, Sarala Suseelan A, Szabo KJ, Schoenebeck F, Maiti D. Orthogonal Selectivity in C–H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution Acs Catalysis. 9: 9606-9613. DOI: 10.1021/Acscatal.9B03019 |
0.822 |
|
| 2019 |
Agasti S, Maiti S, Maity S, Anniyappan M, Talawar M, Maiti D. Bismuth nitrate as a source of nitro radical in ipso-nitration of carboxylic acids Polyhedron. 172: 120-124. DOI: 10.1016/J.Poly.2019.04.005 |
0.805 |
|
| 2019 |
Dey A, Sinha SK, Achar TK, Maiti D. Game of Directors: Accessing Remote Meta‐ and Para‐C‐‐H Bonds With Covalently Attached Directing Groups Angewandte Chemie. 131: 10934-10958. DOI: 10.1002/Ange.201812116 |
0.756 |
|
| 2019 |
Thrimurtulu N, Dey A, Singh A, Pal K, Maiti D, Volla CMR. Palladium Catalyzed Regioselective C4‐Arylation and Olefination of Indoles and Azaindoles Advanced Synthesis & Catalysis. 361: 1441-1446. DOI: 10.1002/Adsc.201801378 |
0.482 |
|
| 2018 |
Bhattacharya T, Pimparkar S, Maiti D. Combining transition metals and transient directing groups for C-H functionalizations. Rsc Advances. 8: 19456-19464. PMID 35541005 DOI: 10.1039/c8ra03230k |
0.854 |
|
| 2018 |
Dey A, Sinha SK, Achar TK, Maiti D. Game of Directors: Accessing Remote Meta- and Para-C--H Bonds With Covalently Attached Directing Groups. Angewandte Chemie (International Ed. in English). PMID 30496638 DOI: 10.1002/Anie.201812116 |
0.844 |
|
| 2018 |
Rana S, Biswas JP, Sen A, Clémancey M, Blondin G, Latour JM, Rajaraman G, Maiti D. Selective C-H halogenation over hydroxylation by non-heme iron(iv)-oxo. Chemical Science. 9: 7843-7858. PMID 30429994 DOI: 10.1039/C8Sc02053A |
0.811 |
|
| 2018 |
Brochetta M, Borsari T, Gandini A, Porey S, Deb A, Casali E, Chakraborty A, Zanoni G, Maiti D. Trifluoromethylation of Allenes: An Expedient Access to α-Trifluoromethylated Enones at Room Temperature. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30414281 DOI: 10.1002/Chem.201805097 |
0.806 |
|
| 2018 |
Maiti D, Achar TK, Ramakrishna K, Pal T, Porey S, Dolui P, Biswas JP. Regiocontrolled Remote C-H Olefination of Small Heterocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30184288 DOI: 10.1002/Chem.201804351 |
0.848 |
|
| 2018 |
Maji A, Dahiya A, Lu G, Bhattacharya T, Brochetta M, Zanoni G, Liu P, Maiti D. H-bonded reusable template assisted para-selective ketonisation using soft electrophilic vinyl ethers. Nature Communications. 9: 3582. PMID 30181575 DOI: 10.1038/S41467-018-06018-2 |
0.797 |
|
| 2018 |
Khan FF, Sinha SK, Lahiri GK, Maiti D. Ruthenium Mediated Distal C-H Activation. Chemistry, An Asian Journal. PMID 29729215 DOI: 10.1002/Asia.201800545 |
0.773 |
|
| 2018 |
Jayarajan R, Das J, Bag S, Chowdhury R, Maiti D. Diverse Meta-C-H Functionalization of Arenes Across Different Linker Lengths. Angewandte Chemie (International Ed. in English). PMID 29700917 DOI: 10.1002/Anie.201804043 |
0.849 |
|
| 2018 |
Maiti D, Lahiri GK, Ray R, Singha Hazari A. Ruthenium Catalyzed Aerobic Oxidation of Amines. Chemistry, An Asian Journal. PMID 29345861 DOI: 10.1002/Asia.201701748 |
0.556 |
|
| 2018 |
Bhattacharya T, Pimparkar S, Maiti D. Combining transition metals and transient directing groups for C–H functionalizations Rsc Advances. 8: 19456-19464. DOI: 10.1039/C8Ra03230K |
0.791 |
|
| 2018 |
Maji A, Reddi Y, Sunoj RB, Maiti D. Mechanistic Insights on Orthogonal Selectivity in Heterocycle Synthesis Acs Catalysis. 8: 10111-10118. DOI: 10.1021/Acscatal.8B02537 |
0.694 |
|
| 2018 |
Guin S, Deb A, Dolui P, Chakraborty S, Singh VK, Maiti D. Promoting Highly Diastereoselective γ-C–H Chalcogenation of α-Amino Acids and Aliphatic Carboxylic Acids Acs Catalysis. 8: 2664-2669. DOI: 10.1021/Acscatal.7B04074 |
0.808 |
|
| 2018 |
Sasmal S, Rana S, Lahiri GK, Maiti D. Manganese-salen catalyzed oxidative benzylic chlorination Journal of Chemical Sciences. 130. DOI: 10.1007/S12039-018-1511-7 |
0.712 |
|
| 2018 |
Sinha SK, Zanoni G, Maiti D. Natural Product Synthesis by C−H Activation Asian Journal of Organic Chemistry. 7: 1178-1192. DOI: 10.1002/Ajoc.201800203 |
0.314 |
|
| 2017 |
Mahato SK, Bhaumik M, Maji A, Dutta A, Maiti D, Maity A. Fe-polyaniline composite nanofiber catalyst for chemoselective hydrolysis of oxime. Journal of Colloid and Interface Science. 513: 592-601. PMID 29195179 DOI: 10.1016/J.Jcis.2017.11.059 |
0.611 |
|
| 2017 |
Maiti D, Lahiri GK, Ray R, Singha Hazari A, Chandra S. Highly Selective Ruthenium Catalyzed Direct Oxygenation of Amines to Amides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29193467 DOI: 10.1002/Chem.201705601 |
0.586 |
|
| 2017 |
Ametovski J, Dutta U, Burchill L, Maiti D, Lupton DW, Hooper JF. Phosphine catalysed (5 + 1) annulation of ynone/cinnamates with primary amines. Chemical Communications (Cambridge, England). PMID 29165450 DOI: 10.1039/C7Cc08252E |
0.82 |
|
| 2017 |
Thrimurtulu N, Khan S, Maity S, Volla CMR, Maiti D. Palladium catalyzed direct aliphatic γC(sp(3))-H alkenylation with alkenes and alkenyl iodides. Chemical Communications (Cambridge, England). PMID 29104971 DOI: 10.1039/C7Cc05703B |
0.806 |
|
| 2017 |
Srinivasan R, Dey A, Nagarajan NS, Kumaran RS, Gandhi T, Maiti D. Pd-Catalyzed C-H arylation of pyridazine-based fused 1,2,4-triazoles: overriding selectivity at the usual position by undermining of preferred chelate formation. Chemical Communications (Cambridge, England). PMID 29022631 DOI: 10.1039/C7Cc06226E |
0.831 |
|
| 2017 |
Maji A, Guin S, Feng S, Dahiya A, Singh VK, Liu P, Maiti D. Experimental and Computational Exploration of Para-Selective Silylation Involving H-Bonded Template. Angewandte Chemie (International Ed. in English). PMID 28986959 DOI: 10.1002/Anie.201708449 |
0.823 |
|
| 2017 |
Maity S, Dolui P, Kancherla R, Maiti D. Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction. Chemical Science. 8: 5181-5185. PMID 28970904 DOI: 10.1039/C7Sc01204G |
0.829 |
|
| 2017 |
Gholap AVA, Maity S, Schulzke C, Maiti D, Kapdi AR. Synthesis of Cu-catalysed quinazolinones using a Csp3-H functionalisation/cyclisation strategy. Organic & Biomolecular Chemistry. PMID 28805837 DOI: 10.1039/C7Ob01723E |
0.788 |
|
| 2017 |
Bag S, Jayarajan R, Dutta U, Chowdhury R, Mondal R, Maiti D. Remote meta-C-H cyanation of arenes enabled by pyrimidine-based auxiliary. Angewandte Chemie (International Ed. in English). PMID 28800387 DOI: 10.1002/Anie.201706360 |
0.854 |
|
| 2017 |
Agasti S, Dey A, Maiti D. Palladium-catalyzed benzofuran and indole synthesis by multiple C-H functionalizations. Chemical Communications (Cambridge, England). PMID 28569899 DOI: 10.1039/C7Cc02053H |
0.852 |
|
| 2017 |
Bera M, Agasti S, Chowdhury R, Mondal R, Pal D, Maiti D. Rhodium-Catalyzed meta-C-H Functionalization of Arenes. Angewandte Chemie (International Ed. in English). PMID 28393438 DOI: 10.1002/Anie.201701579 |
0.868 |
|
| 2017 |
Ray R, Chandra S, Yadav V, Mondal P, Maiti D, Lahiri GK. Ligand controlled switchable selectivity in ruthenium catalyzed aerobic oxidation of primary amines. Chemical Communications (Cambridge, England). PMID 28338149 DOI: 10.1039/C6Cc10200J |
0.566 |
|
| 2017 |
Bag S, Jayarajan R, Mondal R, Maiti D. Template-Assisted meta-C-H Alkylation and Alkenylation of Arenes. Angewandte Chemie (International Ed. in English). PMID 28206690 DOI: 10.1002/Anie.201611360 |
0.842 |
|
| 2017 |
Deb A, Singh S, Seth K, Pimparkar S, Bhaskararao B, Guin S, Sunoj RB, Maiti D. Experimental and Computational Studies on Remote γ-C(sp3)–H Silylation and Germanylation of Aliphatic Carboxamides Acs Catalysis. 7: 8171-8175. DOI: 10.1021/Acscatal.7B03056 |
0.821 |
|
| 2017 |
Seth K, Bera M, Brochetta M, Agasti S, Das A, Gandini A, Porta A, Zanoni G, Maiti D. Incorporating Unbiased, Unactivated Aliphatic Alkenes in Pd(II)-Catalyzed Olefination of Benzyl Phosphonamide Acs Catalysis. 7: 7732-7736. DOI: 10.1021/Acscatal.7B02394 |
0.827 |
|
| 2017 |
Dutta U, Modak A, Bhaskararao B, Bera M, Bag S, Mondal A, Lupton DW, Sunoj RB, Maiti D. Catalytic Arene meta-C–H Functionalization Exploiting a Quinoline-Based Template Acs Catalysis. 7: 3162-3168. DOI: 10.1021/Acscatal.7B00247 |
0.819 |
|
| 2017 |
Modak A, Patra T, Chowdhury R, Raul S, Maiti D. Palladium-Catalyzed Remote meta-Selective C–H Bond Silylation and Germanylation Organometallics. 36: 2418-2423. DOI: 10.1021/Acs.Organomet.7B00309 |
0.82 |
|
| 2017 |
Modak A, Rana S, Phukan AK, Maiti D. Palladium-Catalyzed Deformylation Reactions with Detailed Experimental and in Silico Mechanistic Studies European Journal of Organic Chemistry. 2017: 4168-4174. DOI: 10.1002/Ejoc.201700451 |
0.823 |
|
| 2017 |
Patra T, Maiti D. Frontispiece: Decarboxylation as the Key Step in C−C Bond-Forming Reactions Chemistry - a European Journal. 23. DOI: 10.1002/Chem.201783161 |
0.742 |
|
| 2017 |
Dey A, Maiti D, Lahiri GK. Photoelectrocatalytic Reduction of CO2
into C1 Products by Using Modified-Semiconductor-Based Catalyst Systems Asian Journal of Organic Chemistry. 6: 1519-1530. DOI: 10.1002/Ajoc.201700351 |
0.788 |
|
| 2017 |
Dey A, Pimparkar S, Deb A, Guin S, Maiti D. Chelation-Assisted Palladium-Catalyzed γ-Arylation of Aliphatic Carboxylic Acid Derivatives Advanced Synthesis & Catalysis. 359: 1301-1307. DOI: 10.1002/Adsc.201601121 |
0.833 |
|
| 2016 |
Kundu PK, Dhiman M, Modak A, Chowdhury A, Polshettiwar V, Maiti D. Palladium Nanoparticles Supported on Fibrous Silica (KCC-1-PEI/Pd): A Sustainable Nanocatalyst for Decarbonylation Reactions. Chempluschem. 81: 1142-1146. PMID 31964102 DOI: 10.1002/Cplu.201600245 |
0.743 |
|
| 2016 |
Maji A, Bhaskararao B, Singha S, Sunoj RB, Maiti D. Directing group assisted -hydroxylation by C-H activation. Chemical Science. 7: 3147-3153. PMID 29997806 DOI: 10.1039/C5Sc04060D |
0.743 |
|
| 2016 |
Deb A, Peng Q, Hazra A, Paton RS, Maiti D. Detailed Mechanistic Studies on Palladium Catalyzed Selective C-H Olefination with Aliphatic Alkenes: A Significant Influence of Proton Shuttling. Journal of the American Chemical Society. PMID 27997801 DOI: 10.1021/Jacs.6B10309 |
0.728 |
|
| 2016 |
Naveen T, Deb A, Maiti D. Copper/P(tBu)3 -Mediated Regiospecific Synthesis of Fused Furans and Naphthofurans. Angewandte Chemie (International Ed. in English). PMID 27996192 DOI: 10.1002/Anie.201609401 |
0.814 |
|
| 2016 |
Modak A, Mondal A, Watile R, Mukherjee S, Maiti D. Correction: Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives. Chemical Communications (Cambridge, England). PMID 27929150 DOI: 10.1039/c6cc90551j |
0.824 |
|
| 2016 |
Maiti D, Patra T. Decarboxylation as the key step in C-C bond forming reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27859719 DOI: 10.1002/Chem.201604496 |
0.792 |
|
| 2016 |
Maity S, Hoque E, Dhawa U, Maiti D. Palladium catalyzed selective distal C-H olefination of biaryl systems. Chemical Communications (Cambridge, England). PMID 27853761 DOI: 10.1039/C6Cc07861C |
0.854 |
|
| 2016 |
Modak A, Mondal A, Watile R, Mukherjee S, Maiti D. Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives. Chemical Communications (Cambridge, England). PMID 27844064 DOI: 10.1039/C6Cc08302A |
0.856 |
|
| 2016 |
Agasti S, Dey A, Maiti D. Traceless directing group mediated branched selective alkenylation of unbiased arenes. Chemical Communications (Cambridge, England). 52: 12191-12194. PMID 27711336 DOI: 10.1039/C6Cc07032A |
0.848 |
|
| 2016 |
Thrimurtulu N, Dey A, Maiti D, Volla CM. Cobalt-Catalyzed sp(2) -C-H Activation: Intermolecular Heterocyclization with Allenes at Room Temperature. Angewandte Chemie (International Ed. in English). PMID 27584828 DOI: 10.1002/Anie.201604956 |
0.527 |
|
| 2016 |
Dey A, Maity S, Maiti D. Reaching the south: metal-catalyzed transformation of the aromatic para-position. Chemical Communications (Cambridge, England). PMID 27559937 DOI: 10.1039/C6Cc05235E |
0.848 |
|
| 2016 |
Ray R, Chandra S, Maiti D, Lahiri GK. Simple and Efficient Ruthenium-Catalyzed Oxidation of Primary Alcohols with Molecular Oxygen. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27257955 DOI: 10.1002/Chem.201601800 |
0.527 |
|
| 2016 |
Patra T, Bag S, Kancherla R, Mondal A, Dey A, Pimparkar S, Agasti S, Modak A, Maiti D. Palladium-Catalyzed Directed para C-H Functionalization of Phenols. Angewandte Chemie (International Ed. in English). PMID 27159887 DOI: 10.1002/Anie.201601999 |
0.85 |
|
| 2016 |
Dey A, Agasti S, Maiti D. Palladium catalysed meta-C-H functionalization reactions. Organic & Biomolecular Chemistry. PMID 27120353 DOI: 10.1039/C6Ob00395H |
0.866 |
|
| 2016 |
Dutta U, Lupton DW, Maiti D. Aryl Nitriles from Alkynes Using tert-Butyl Nitrite: Metal-Free Approach to C≡C Bond Cleavage. Organic Letters. PMID 26849380 DOI: 10.1021/Acs.Orglett.6B00147 |
0.829 |
|
| 2016 |
Bag S, Maiti D. Palladium-Catalyzed Olefination of Aryl C-H Bonds by Using Directing Scaffolds Synthesis (Germany). 48: 804-815. DOI: 10.1055/S-0035-1561321 |
0.813 |
|
| 2016 |
Dey A, Sasmal S, Seth K, Lahiri GK, Maiti D. Nickel-Catalyzed Deamidative Step-Down Reduction of Amides to Aromatic Hydrocarbons Acs Catalysis. 7: 433-437. DOI: 10.1021/Acscatal.6B03040 |
0.816 |
|
| 2016 |
Maity S, Kancherla R, Dhawa U, Hoque E, Pimparkar S, Maiti D. Switch to Allylic Selectivity in Cobalt-Catalyzed Dehydrogenative Heck Reactions with Unbiased Aliphatic Olefins Acs Catalysis. 6: 5493-5499. DOI: 10.1021/Acscatal.6B01816 |
0.838 |
|
| 2016 |
Bera M, Sahoo SK, Maiti D. Room-Temperature meta-Functionalization: Pd(II)-Catalyzed Synthesis of 1,3,5-Trialkenyl Arene and meta-Hydroxylated Olefin Acs Catalysis. 6: 3575-3579. DOI: 10.1021/Acscatal.6B00675 |
0.742 |
|
| 2016 |
Kumar S, Kumar P, Deb A, Maiti D, Jain SL. Graphene oxide grafted with iridium complex as a superior heterogeneous catalyst for chemical fixation of carbon dioxide to dimethylformamide Carbon. 100: 632-640. DOI: 10.1016/J.Carbon.2016.01.018 |
0.606 |
|
| 2016 |
Deb A, Maiti D. Emergence of Unactivated Olefins for the Synthesis of Olefinated Arenes European Journal of Organic Chemistry. 2017: 1239-1252. DOI: 10.1002/Ejoc.201601253 |
0.665 |
|
| 2016 |
Ray R, Chandra S, Maiti D, Lahiri GK. Frontispiece: Simple and Efficient Ruthenium-Catalyzed Oxidation of Primary Alcohols with Molecular Oxygen Chemistry - a European Journal. 22. DOI: 10.1002/Chem.201682662 |
0.487 |
|
| 2016 |
Rana S, Pandey B, Dey A, Haque R, Rajaraman G, Maiti D. A Doubly Biomimetic Synthetic Transformation: Catalytic Decarbonylation and Halogenation at Room Temperature by Vanadium Pentoxide Chemcatchem. 8: 3367-3374. DOI: 10.1002/Cctc.201600843 |
0.78 |
|
| 2015 |
Patra T, Watile R, Agasti S, Naveen T, Maiti D. Sequential meta-C-H olefination of synthetically versatile benzyl silanes: effective synthesis of meta-olefinated toluene, benzaldehyde and benzyl alcohols. Chemical Communications (Cambridge, England). PMID 26687486 DOI: 10.1039/C5Cc09446A |
0.849 |
|
| 2015 |
Patra T, Nandi S, Sahoo SK, Maiti D. Copper mediated decarboxylative direct C-H arylation of heteroarenes with benzoic acids. Chemical Communications (Cambridge, England). PMID 26647115 DOI: 10.1039/C5Cc08367B |
0.826 |
|
| 2015 |
Modak A, Maiti D. Metal catalyzed defunctionalization reactions. Organic & Biomolecular Chemistry. PMID 26565518 DOI: 10.1039/C5Ob01949D |
0.767 |
|
| 2015 |
Dutta U, Deb A, Lupton DW, Maiti D. The regioselective iodination of quinolines, quinolones, pyridones, pyridines and uracil. Chemical Communications (Cambridge, England). PMID 26489708 DOI: 10.1039/C5Cc07799K |
0.84 |
|
| 2015 |
Bag S, Patra T, Modak A, Deb A, Maity S, Dutta U, Dey A, Kancherla R, Maji A, Hazra A, Bera M, Maiti D. Remote para-C-H Functionalization of Arenes by a D-Shaped Biphenyl Template-Based Assembly. Journal of the American Chemical Society. 137: 11888-91. PMID 26361337 DOI: 10.1021/Jacs.5B06793 |
0.838 |
|
| 2015 |
Agasti S, Maity S, Szabo KJ, Maiti D. Palladium-Catalyzed Synthesis of 2,3-Disubstituted Benzofurans: An Approach Towards the Synthesis of Deuterium Labeled Compounds. Advanced Synthesis & Catalysis. 357: 2331-2338. PMID 26347405 DOI: 10.1002/Adsc.201500308 |
0.825 |
|
| 2015 |
Rana S, Dey A, Maiti D. Mechanistic elucidation of C-H oxidation by electron rich non-heme iron(iv)-oxo at room temperature. Chemical Communications (Cambridge, England). 51: 14469-72. PMID 26277913 DOI: 10.1039/C5Cc04803F |
0.811 |
|
| 2015 |
Maity S, Agasti S, Earsad AM, Hazra A, Maiti D. Nickel-Catalyzed Insertion of Alkynes and Electron-Deficient Olefins into Unactivated sp(3) CH Bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 11320-4. PMID 26121618 DOI: 10.1002/Chem.201501962 |
0.853 |
|
| 2015 |
Bera M, Maji A, Sahoo SK, Maiti D. Palladium(II)-Catalyzed meta-CH Olefination: Constructing Multisubstituted Arenes through Homo-Diolefination and Sequential Hetero-Diolefination. Angewandte Chemie (International Ed. in English). 54: 8515-9. PMID 26060101 DOI: 10.1002/Anie.201503112 |
0.851 |
|
| 2015 |
Kancherla R, Naveen T, Maiti D. Divergent Reactivity in Palladium-Catalyzed Annulation with Diarylamines and α,β-Unsaturated Acids: Direct Access to Substituted 2-Quinolinones and Indoles. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 8723-6. PMID 25941155 DOI: 10.1002/Chem.201501208 |
0.817 |
|
| 2015 |
Kancherla R, Naveen T, Maiti D. Palladium-Catalyzed [3+3] Annulation between Diarylamines and α,β-Unsaturated Acids through C-H Activation: Direct Access to 4-Substituted 2-Quinolinones. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 8360-4. PMID 25899388 DOI: 10.1002/Chem.201500774 |
0.835 |
|
| 2015 |
Modak A, Rana S, Maiti D. Iron-Catalyzed Regioselective Direct Arylation at the C-3 Position of N-Alkyl-2-pyridone. The Journal of Organic Chemistry. 80: 296-303. PMID 25423099 DOI: 10.1021/Jo502362K |
0.848 |
|
| 2015 |
Khamarui S, Maiti R, Maiti DK. General base-tuned unorthodox synthesis of amides and ketoesters with water. Chemical Communications (Cambridge, England). 51: 384-7. PMID 25406587 DOI: 10.1039/c4cc07961b |
0.333 |
|
| 2015 |
Agasti S, Sharma U, Naveen T, Maiti D. Orthogonal selectivity with cinnamic acids in 3-substituted benzofuran synthesis through C-H olefination of phenols. Chemical Communications (Cambridge, England). 51: 5375-8. PMID 25347298 DOI: 10.1039/C4Cc07026G |
0.856 |
|
| 2015 |
Modak A, Rana S, Maiti D. C-3 Arylation of N-Alkyl-2-pyridones Synfacts. 11: 311-311. DOI: 10.1055/S-0034-1380034 |
0.811 |
|
| 2015 |
Modak A, Rana S, Maiti D. ChemInform Abstract: Iron-Catalyzed Regioselective Direct Arylation at the C-3 Position of N-Alkyl-2-pyridone. Cheminform. 46: no-no. DOI: 10.1002/chin.201521174 |
0.62 |
|
| 2015 |
Agasti S, Maity S, Szabo KJ, Maiti D. Palladium-Catalyzed Synthesis of 2,3-Disubstituted Benzofurans: An Approach Towards the Synthesis of Deuterium Labeled Compounds Advanced Synthesis and Catalysis. 357: 2331-2338. DOI: 10.1002/adsc.201500308 |
0.69 |
|
| 2015 |
Sharma U, Modak A, Maity S, Maji A, Maiti D. Direct arylation via C-H activation Rsc Catalysis Series. 2015: 551-609. |
0.692 |
|
| 2014 |
Dutta U, Maity S, Kancherla R, Maiti D. Aerobic oxynitration of alkynes with (t)BuONO and TEMPO. Organic Letters. 16: 6302-5. PMID 25401303 DOI: 10.1021/Ol503025N |
0.816 |
|
| 2014 |
Bera M, Modak A, Patra T, Maji A, Maiti D. Meta-selective arene C-H bond olefination of arylacetic acid using a nitrile-based directing group. Organic Letters. 16: 5760-3. PMID 25310718 DOI: 10.1021/Ol502823C |
0.855 |
|
| 2014 |
Ray R, Jana RD, Bhadra M, Maiti D, Lahiri GK. Efficient and simple approaches towards direct oxidative esterification of alcohols. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 15618-24. PMID 25284591 DOI: 10.1002/Chem.201403786 |
0.79 |
|
| 2014 |
Naveen T, Kancherla R, Maiti D. Radical based strategy toward the synthesis of 2,3-dihydrofurans from aryl ketones and aromatic olefins. Organic Letters. 16: 5446-9. PMID 25275799 DOI: 10.1021/Ol502688R |
0.824 |
|
| 2014 |
Sharma U, Kancherla R, Naveen T, Agasti S, Maiti D. Palladium-catalyzed annulation of diarylamines with olefins through C-H activation: direct access to N-arylindoles. Angewandte Chemie (International Ed. in English). 53: 11895-9. PMID 25204895 DOI: 10.1002/Anie.201406284 |
0.852 |
|
| 2014 |
Deb A, Bag S, Kancherla R, Maiti D. Palladium-catalyzed aryl C-H olefination with unactivated, aliphatic alkenes. Journal of the American Chemical Society. 136: 13602-5. PMID 25188679 DOI: 10.1021/Ja5082734 |
0.871 |
|
| 2014 |
Maji A, Hazra A, Maiti D. Direct synthesis of α-trifluoromethyl ketone from (hetero)arylacetylene: design, intermediate trapping, and mechanistic investigations. Organic Letters. 16: 4524-7. PMID 25127202 DOI: 10.1021/Ol502071G |
0.656 |
|
| 2014 |
Modak A, Dutta U, Kancherla R, Maity S, Bhadra M, Mobin SM, Maiti D. Predictably selective (sp3)C-O bond formation through copper catalyzed dehydrogenative coupling: facile synthesis of dihydro-oxazinone derivatives. Organic Letters. 16: 2602-5. PMID 24761793 DOI: 10.1021/Ol500670H |
0.818 |
|
| 2014 |
Maji A, Rana S, Akanksha, Maiti D. Synthesis of bis(heteroaryl) ketones by removal of benzylic CHR and CO groups. Angewandte Chemie (International Ed. in English). 53: 2428-32. PMID 24481978 DOI: 10.1002/Anie.201308785 |
0.763 |
|
| 2014 |
Samanta S, Roy D, Khamarui S, Maiti DK. Ni(II)-salt catalyzed activation of primary amine-sp(3)Cα-H and cyclization with 1,2-diketone to tetrasubstituted imidazoles. Chemical Communications (Cambridge, England). 50: 2477-80. PMID 24457458 DOI: 10.1039/c3cc48437h |
0.424 |
|
| 2014 |
Ray R, Chowdhury AD, Maiti D, Lahiri GK. Iron catalysed nitrosation of olefins to oximes. Dalton Transactions (Cambridge, England : 2003). 43: 38-41. PMID 24158361 DOI: 10.1039/C3Dt51764K |
0.563 |
|
| 2014 |
Snieckus V, Kim J, Modak A, Dutta U, Kancherla R, Maity S, Bhadra M, Mobin SM, Maiti D. Dihydro-oxazinones from Salicylamides Synfacts. 10: 683-683. DOI: 10.1055/S-0034-1378255 |
0.798 |
|
| 2014 |
Maity S, Naveen T, Sharma U, Maiti D. Efficient and stereoselective nitration of olefins with AgNO2 and TEMPO Synlett. 25: 603-607. DOI: 10.1055/S-0033-1340467 |
0.825 |
|
| 2014 |
Rana S, Bag S, Patra T, Maiti D. Catalytic electrophilic halogenations and haloalkoxylations by non-heme iron halides Advanced Synthesis and Catalysis. 356: 2453-2458. DOI: 10.1002/Adsc.201400316 |
0.773 |
|
| 2014 |
Deb A, Agasti S, Saboo T, Maiti D. Generation of arylated quinones by iron-catalyzed oxidative arylation of phenols: Formal synthesis of phellodonin, sarcodonin ε, leucomelone and betulinan A Advanced Synthesis and Catalysis. 356: 705-710. DOI: 10.1002/Adsc.201301084 |
0.778 |
|
| 2014 |
Rana S, Modak A, Maity S, Patra T, Maiti D. Iron Catalysis in Synthetic Chemistry Progress in Inorganic Chemistry. 59: 1-188. DOI: 10.1002/9781118869994.ch01 |
0.753 |
|
| 2013 |
Ghosh S, Khamarui S, Gayen KS, Maiti DK. ArCH(OMe)₂--a Pt(IV)-catalyst originator for diverse annulation catalysis. Scientific Reports. 3: 2987. PMID 24136161 DOI: 10.1038/srep02987 |
0.396 |
|
| 2013 |
Sharma U, Naveen T, Maji A, Manna S, Maiti D. Palladium-catalyzed synthesis of benzofurans and coumarins from phenols and olefins. Angewandte Chemie (International Ed. in English). 52: 12669-73. PMID 24127393 DOI: 10.1002/Anie.201305326 |
0.831 |
|
| 2013 |
Sengupta T, Khamarui S, Samanta S, Maiti DK. Synthetically useful noncatalytic strategy: a stereocontrolled rapid cyclization of a three component system to afford hexahydropyrrolizines. Chemical Communications (Cambridge, England). 49: 9962-4. PMID 24037123 DOI: 10.1039/c3cc45820b |
0.413 |
|
| 2013 |
Deb A, Manna S, Modak A, Patra T, Maity S, Maiti D. Oxidative trifluoromethylation of unactivated olefins: an efficient and practical synthesis of α-trifluoromethyl-substituted ketones. Angewandte Chemie (International Ed. in English). 52: 9747-50. PMID 23934929 DOI: 10.1002/Anie.201303576 |
0.797 |
|
| 2013 |
Patra T, Agasti S, Modak A, Maiti D. Nickel-catalyzed hydrogenolysis of unactivated carbon-cyano bonds. Chemical Communications (Cambridge, England). 49: 8362-4. PMID 23928690 DOI: 10.1039/C3Cc44562C |
0.855 |
|
| 2013 |
Maity S, Naveen T, Sharma U, Maiti D. Stereoselective nitration of olefins with (t)BuONO and TEMPO: direct access to nitroolefins under metal-free conditions. Organic Letters. 15: 3384-7. PMID 23772945 DOI: 10.1021/Ol401426P |
0.817 |
|
| 2013 |
Naveen T, Maity S, Sharma U, Maiti D. A predictably selective nitration of olefin with Fe(NO3)3 and TEMPO. The Journal of Organic Chemistry. 78: 5949-54. PMID 23692506 DOI: 10.1021/Jo400598P |
0.814 |
|
| 2013 |
Manna S, Jana S, Saboo T, Maji A, Maiti D. Synthesis of (E)-nitroolefins via decarboxylative nitration using t-butylnitrite (t-BuONO) and TEMPO. Chemical Communications (Cambridge, England). 49: 5286-8. PMID 23636417 DOI: 10.1039/C3Cc41576G |
0.779 |
|
| 2013 |
Rana S, Haque R, Santosh G, Maiti D. Decarbonylative halogenation by a vanadium complex. Inorganic Chemistry. 52: 2927-32. PMID 23458249 DOI: 10.1021/Ic302611A |
0.67 |
|
| 2013 |
Maity S, Manna S, Rana S, Naveen T, Mallick A, Maiti D. Efficient and stereoselective nitration of mono- and disubstituted olefins with AgNO2 and TEMPO. Journal of the American Chemical Society. 135: 3355-8. PMID 23406020 DOI: 10.1021/Ja311942E |
0.812 |
|
| 2013 |
Modak A, Naveen T, Maiti D. An efficient dehydroxymethylation reaction by a palladium catalyst. Chemical Communications (Cambridge, England). 49: 252-4. PMID 23164948 DOI: 10.1039/C2Cc36951F |
0.821 |
|
| 2013 |
Patra T, Agasti S, Akanksha, Maiti D. Nickel-catalyzed decyanation of inert carbon-cyano bonds. Chemical Communications (Cambridge, England). 49: 69-71. PMID 23152958 DOI: 10.1039/C2Cc36883H |
0.825 |
|
| 2013 |
Deb A, Manna S, Maji A, Dutta U, Maiti D. Iron-catalyzed direct C-H arylation of heterocycles and quinones with arylboronic acids European Journal of Organic Chemistry. 5251-5256. DOI: 10.1002/Ejoc.201300743 |
0.845 |
|
| 2013 |
Patra T, Deb A, Manna S, Sharma U, Maiti D. Iron-mediated decarboxylative trifluoromethylation of α,β- unsaturated carboxylic acids with trifluoromethanesulfinate European Journal of Organic Chemistry. 5247-5250. DOI: 10.1002/Ejoc.201300473 |
0.799 |
|
| 2012 |
Dhara D, Gayen KS, Khamarui S, Pandit P, Ghosh S, Maiti DK. CeCl3·7H2O catalyzed C-C and C-N bond-forming cascade cyclization with subsequent side-chain functionalization and rearrangement: a domino approach to pentasubstituted pyrrole analogues. The Journal of Organic Chemistry. 77: 10441-9. PMID 23113545 DOI: 10.1021/jo301796r |
0.468 |
|
| 2012 |
Saima Y, Khamarui S, Gayen KS, Pandit P, Maiti DK. Efficient catalytic cyclizations of three and two imine assemblies: direct access to tetrahydroimidazo[1,5-c]imidazol-7-ones and imidazoles. Chemical Communications (Cambridge, England). 48: 6601-3. PMID 22627840 DOI: 10.1039/c2cc32760k |
0.364 |
|
| 2012 |
Modak A, Deb A, Patra T, Rana S, Maity S, Maiti D. A general and efficient aldehyde decarbonylation reaction by using a palladium catalyst. Chemical Communications (Cambridge, England). 48: 4253-5. PMID 22441208 DOI: 10.1039/C2Cc31144E |
0.813 |
|
| 2012 |
Manna S, Maity S, Rana S, Agasti S, Maiti D. ipso-Nitration of arylboronic acids with bismuth nitrate and perdisulfate. Organic Letters. 14: 1736-9. PMID 22409632 DOI: 10.1021/Ol300325T |
0.805 |
|
| 2012 |
Sengupta T, Gayen KS, Pandit P, Maiti DK. FeCl3â‹…6H2O-catalyzed intermolecular-cascade cyclization of acetoacetanilide: aldehyde-tuned synthesis to valuable 2-pyridone analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 1905-9. PMID 22266708 DOI: 10.1002/chem.201103354 |
0.364 |
|
| 2012 |
Akanksha, Maiti D. Microwave-assisted palladium mediated decarbonylation reaction: Synthesis of eulatachromene Green Chemistry. 14: 2314-2320. DOI: 10.1039/C2Gc35622H |
0.399 |
|
| 2011 |
Maiti D, Fors BP, Henderson JL, Nakamura Y, Buchwald SL. Palladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most Cases. Chemical Science. 2: 57-68. PMID 22384311 DOI: 10.1039/C0Sc00330A |
0.739 |
|
| 2011 |
Patra T, Manna S, Maiti D. Metal-mediated deformylation reactions: synthetic and biological avenues. Angewandte Chemie (International Ed. in English). 50: 12140-2. PMID 22025479 DOI: 10.1002/Anie.201103860 |
0.858 |
|
| 2011 |
Maiti D. Chemoselectivity in the Cu-catalyzed O-arylation of phenols and aliphatic alcohols. Chemical Communications (Cambridge, England). 47: 8340-2. PMID 21698330 DOI: 10.1039/C1Cc12694F |
0.365 |
|
| 2011 |
Pandit P, Chatterjee N, Maiti DK. First synthesis of fused-Δ1-pyrrolines via intramolecular 1,3-dipolar cycloaddition of ketoimine: a complete diastereoselective approach. Chemical Communications (Cambridge, England). 47: 1285-7. PMID 21103501 DOI: 10.1039/c0cc03873c |
0.302 |
|
| 2011 |
Patra T, Manna S, Maiti D. Metallvermittelte Deformylierungen in Synthese und Biologie Angewandte Chemie. 123: 12344-12346. DOI: 10.1002/Ange.201103860 |
0.785 |
|
| 2010 |
Woertink JS, Tian L, Maiti D, Lucas HR, Himes RA, Karlin KD, Neese F, Würtele C, Holthausen MC, Bill E, Sundermeyer J, Schindler S, Solomon EI. Spectroscopic and computational studies of an end-on bound superoxo-Cu(II) complex: geometric and electronic factors that determine the ground state. Inorganic Chemistry. 49: 9450-9. PMID 20857998 DOI: 10.1021/Ic101138U |
0.718 |
|
| 2010 |
Maiti DK, Chatterjee N, Pandit P, Hota SK. Generation of azomethine imine and metal-free formal 1,3-dipolar cycloaddition of imine with PhIO: reaction, scope, and synthesis. Chemical Communications (Cambridge, England). 46: 2022-4. PMID 20221479 DOI: 10.1039/b924761k |
0.315 |
|
| 2010 |
Maiti D, Buchwald SL. Cu-catalyzed arylation of phenols: synthesis of sterically hindered and heteroaryl diaryl ethers. The Journal of Organic Chemistry. 75: 1791-4. PMID 20141182 DOI: 10.1021/Jo9026935 |
0.529 |
|
| 2009 |
Maiti D, Buchwald SL. Orthogonal Cu- and Pd-based catalyst systems for the O- and N-arylation of aminophenols. Journal of the American Chemical Society. 131: 17423-9. PMID 19899753 DOI: 10.1021/Ja9081815 |
0.516 |
|
| 2009 |
Maiti D, Woertink JS, Ghiladi RA, Solomon EI, Karlin KD. Molecular oxygen and sulfur reactivity of a cyclotriveratrylene derived trinuclear copper(I) complex. Inorganic Chemistry. 48: 8342-56. PMID 19663454 DOI: 10.1021/Ic900975Y |
0.665 |
|
| 2008 |
Maiti D, Narducci Sarjeant AA, Karlin KD. Copper-hydroperoxo-mediated N-debenzylation chemistry mimicking aspects of copper monooxygenases. Inorganic Chemistry. 47: 8736-47. PMID 18783212 DOI: 10.1021/Ic800617M |
0.604 |
|
| 2008 |
Maiti D, Lee DH, Narducci Sarjeant AA, Pau MY, Solomon EI, Gaoutchenova K, Sundermeyer J, Karlin KD. Reaction of a copper-dioxygen complex with nitrogen monoxide (*NO) leads to a copper(II)-peroxynitrite species. Journal of the American Chemical Society. 130: 6700-1. PMID 18457392 DOI: 10.1021/Ja801540E |
0.484 |
|
| 2008 |
Maiti D, Woertink JS, Narducci Sarjeant AA, Solomon EI, Karlin KD. Copper dioxygen adducts: formation of bis(mu-oxo)dicopper(III) versus (mu-1,2)Peroxodicopper(II) complexes with small changes in one pyridyl-ligand substituent. Inorganic Chemistry. 47: 3787-800. PMID 18396862 DOI: 10.1021/Ic702437C |
0.631 |
|
| 2008 |
Maiti D, Narducci Sarjeant AA, Itoh S, Karlin KD. Suggestion of an organometallic intermediate in an intramolecular dechlorination reaction involving copper(I) and a ArCH2Cl moiety. Journal of the American Chemical Society. 130: 5644-5. PMID 18393421 DOI: 10.1021/Ja800795B |
0.677 |
|
| 2008 |
Maiti D, Lee DH, Gaoutchenova K, Würtele C, Holthausen MC, Sarjeant AA, Sundermeyer J, Schindler S, Karlin KD. Reactions of a copper(II) superoxo complex lead to C-H and O-H substrate oxygenation: modeling copper-monooxygenase C-H hydroxylation. Angewandte Chemie (International Ed. in English). 47: 82-5. PMID 18022887 DOI: 10.1002/Anie.200704389 |
0.698 |
|
| 2007 |
Maiti D, Woertink JS, Vance MA, Milligan AE, Sarjeant AA, Solomon EI, Karlin KD. Copper(I)/S(8) reversible reactions leading to an end-on bound dicopper(II) disulfide complex: nucleophilic reactivity and analogies to copper-dioxygen chemistry. Journal of the American Chemical Society. 129: 8882-92. PMID 17592845 DOI: 10.1021/Ja071968Z |
0.482 |
|
| 2007 |
Maiti D, Lucas HR, Sarjeant AA, Karlin KD. Aryl hydroxylation from a mononuclear copper-hydroperoxo species. Journal of the American Chemical Society. 129: 6998-9. PMID 17497785 DOI: 10.1021/Ja071704C |
0.745 |
|
| 2007 |
Maiti D, Sarjeant AA, Karlin KD. Copper(II)-hydroperoxo complex induced oxidative N-dealkylation chemistry. Journal of the American Chemical Society. 129: 6720-1. PMID 17474748 DOI: 10.1021/Ja0719024 |
0.531 |
|
| 2007 |
Maiti D, Fry HC, Woertink JS, Vance MA, Solomon EI, Karlin KD. A 1:1 copper-dioxygen adduct is an end-on bound superoxo copper(II) complex which undergoes oxygenation reactions with phenols. Journal of the American Chemical Society. 129: 264-5. PMID 17212392 DOI: 10.1021/Ja067411L |
0.676 |
|
| 2006 |
Helton ME, Maiti D, Zakharov LN, Rheingold AL, Porco JA, Karlin KD. A mu-eta2:eta2-disulfide dicopper(II) complex from reaction of S8 with a copper(I) precursor: reactivity of the bound disulfur moiety. Angewandte Chemie (International Ed. in English). 45: 1138-41. PMID 16385608 DOI: 10.1002/Anie.200503216 |
0.512 |
|
| 2004 |
Maiti D, Paul H, Chanda N, Chakraborty S, Mondal B, Puranik VG, Lahiri GK. Synthesis, structure, spectral and electron-transfer properties of octahedral-[CoIII(L)2]+/[ZnII(L) 2] and square planar-[CuII(L){OC(=O)CH3}] complexes incorporating anionic form of tridentate bis(8-quinolinyl)amine [N1C9H6-N2-C9H 6N3, L-] ligand Polyhedron. 23: 831-840. DOI: 10.1016/J.Poly.2003.11.053 |
0.709 |
|
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