| Year |
Citation |
Score |
| 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 |
0.821 |
|
| 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 |
0.768 |
|
| 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 |
0.678 |
|
| 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 |
0.673 |
|
| 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 |
0.675 |
|
| 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 |
0.766 |
|
| 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 |
0.708 |
|
| 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 |
0.747 |
|
| 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 |
0.807 |
|
| 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 |
0.791 |
|
| 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 |
0.825 |
|
| 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 |
0.817 |
|
| 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 |
0.823 |
|
| 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 |
0.783 |
|
| 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 |
0.816 |
|
| 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 |
0.678 |
|
| 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 |
0.714 |
|
| 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 |
0.802 |
|
| 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 |
0.821 |
|
| 2016 |
Majji G, Rout SK, Rajamanickam S, Guin S, Patel BK. Synthesis of esters via sp(3) C-H functionalisation. Organic & Biomolecular Chemistry. PMID 27488288 DOI: 10.1039/C6Ob01250G |
0.826 |
|
| 2016 |
Gogoi A, Sau P, Ali W, Guin S, Patel BK. Copper(II)-Catalyzed Synthesis of Indoloquinoxalin-6-ones through Oxidative Mannich Reaction European Journal of Organic Chemistry. 2016: 1449-1453. DOI: 10.1002/Ejoc.201501532 |
0.765 |
|
| 2016 |
Majji G, Rout SK, Rajamanickam S, Guin S, Patel BK. ChemInform Abstract: Synthesis of Esters via sp3C-H Functionalization Cheminform. 47. DOI: 10.1002/CHIN.201644207 |
0.807 |
|
| 2016 |
Gogoi A, Sau P, Ali W, Guin S, Patel BK. ChemInform Abstract: Copper(II)-Catalyzed Synthesis of Indoloquinoxalin-6-ones Through Oxidative Mannich Reaction. Cheminform. 47. DOI: 10.1002/CHIN.201629152 |
0.716 |
|
| 2015 |
Gogoi A, Guin S, Rajamanickam S, Rout SK, Patel BK. Synthesis of 1,2,4-Triazoles via Oxidative Heterocyclization: Selective C-N Bond Over C-S Bond Formation. The Journal of Organic Chemistry. 80: 9016-27. PMID 26332253 DOI: 10.1021/Acs.Joc.5B00956 |
0.826 |
|
| 2015 |
Ali W, Behera A, Guin S, Patel BK. Regiospecific Benzoylation of Electron-Deficient N-Heterocycles with Methylbenzenes via a Minisci-Type Reaction. The Journal of Organic Chemistry. 80: 5625-32. PMID 25938383 DOI: 10.1021/Acs.Joc.5B00501 |
0.788 |
|
| 2015 |
Behera A, Ali W, Guin S, Khatun N, Mohanta PR, Patel BK. Benzyl bromides as aroyl surrogates in substrate directed Pd catalysed o-aroylation Rsc Advances. 5: 33334-33338. DOI: 10.1039/C5Ra03836G |
0.77 |
|
| 2015 |
Behera A, Ali W, Guin S, Khatun N, Mohanta PR, Patel BK. ChemInform Abstract: Benzyl Bromides as Aroyl Surrogates in Substrate Directed Pd Catalyzed O-Aroylation. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201535088 |
0.756 |
|
| 2015 |
Ali W, Rout SK, Guin S, Modi A, Banerjee A, Patel BK. ChemInform Abstract: Copper-Catalyzed Cross Dehydrogenative Coupling of N,N-Disubstituted Formamides and Phenols: A Direct Access to Carbamates. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201525113 |
0.789 |
|
| 2015 |
Gogoi A, Guin S, Rout SK, Majji G, Patel BK. ChemInform Abstract: A Cu-Catalyzed Synthesis of Substituted 3-Methyleneisoindolin-1-one. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201519153 |
0.739 |
|
| 2015 |
Behera A, Rout SK, Guin S, Patel BK. ChemInform Abstract: Benzylamine as an Arylcarboxy Surrogate: A Copper Catalyzed o-Benzoxylation of 2-Phenylpyridines Using Benzyl Amines. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201517204 |
0.794 |
|
| 2015 |
Ali W, Guin S, Rout SK, Gogoi A, Patel BK. ChemInform Abstract: Thioesterification of Alkylbenzenes with Thiols via Copper-Catalyzed Cross-Dehydrogenative Coupling Without a Directing Group. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201511104 |
0.79 |
|
| 2015 |
Guin S, Rout SK, Gogoi A, Ali W, Patel BK. ChemInform Abstract: A Palladium(II)-Catalyzed Synthesis of α-Ketoamides via Chemoselective Aroyl Addition to Cyanamides. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201507093 |
0.79 |
|
| 2015 |
Ali W, Rout SK, Guin S, Modi A, Banerjee A, Patel BK. Copper-catalyzed cross dehydrogenative coupling of N,N-disubstituted formamides and phenols: A direct access to carbamates Advanced Synthesis and Catalysis. 357: 515-522. DOI: 10.1002/Adsc.201400659 |
0.842 |
|
| 2014 |
Majji G, Guin S, Rout SK, Behera A, Patel BK. Cyclic ethers to esters and monoesters to bis-esters with unconventional coupling partners under metal free conditions via sp(3) C-H functionalisation. Chemical Communications (Cambridge, England). 50: 12193-6. PMID 25177921 DOI: 10.1039/C4Cc05050A |
0.824 |
|
| 2014 |
Gogoi A, Modi A, Guin S, Rout SK, Das D, Patel BK. A metal free domino synthesis of 3-aroylindoles via two sp³ C-H activation. Chemical Communications (Cambridge, England). 50: 10445-7. PMID 25061987 DOI: 10.1039/C4Cc04407J |
0.822 |
|
| 2014 |
Rout SK, Guin S, Ali W, Gogoi A, Patel BK. Copper-catalyzed esterification of alkylbenzenes with cyclic ethers and cycloalkanes via C(sp3)-H activation following cross-dehydrogenative coupling. Organic Letters. 16: 3086-9. PMID 24852383 DOI: 10.1021/Ol5011906 |
0.84 |
|
| 2014 |
Rout SK, Guin S, Gogoi A, Majji G, Patel BK. Terminal aryl alkenes and alkynes as arylcarboxy surrogates toward o-benzoxylation of 2-phenylpyridine catalyzed by copper. Organic Letters. 16: 1614-7. PMID 24588713 DOI: 10.1021/Ol500224E |
0.769 |
|
| 2014 |
Gogoi A, Guin S, Rout SK, Majji G, Patel BK. A Cu-catalysed synthesis of substituted 3-methyleneisoindolin-1-one Rsc Advances. 4: 59902-59907. DOI: 10.1039/C4Ra12782J |
0.776 |
|
| 2014 |
Behera A, Rout SK, Guin S, Patel BK. Benzylamine as an arylcarboxy surrogate: A copper catalysed o-benzoxylation of 2-phenylpyridines using benzyl amines Rsc Advances. 4: 55115-55118. DOI: 10.1039/C4Ra09922B |
0.803 |
|
| 2014 |
Khatun N, Guin S, Rout SK, Patel BK. Divergent reactivities of o-haloanilides with CuO nanoparticles in water: A green synthesis of benzoxazoles and o-hydroxyanilides Rsc Advances. 4: 10770-10778. DOI: 10.1039/C3Ra46820H |
0.728 |
|
| 2014 |
Banerjee A, Bera A, Santra SK, Guin S, Patel BK. Palladium-catalysed regioselective aroylation and acetoxylation of 3,5-diarylisoxazole via ortho C–H functionalisations Rsc Advances. 4: 8558. DOI: 10.1039/C3Ra45403G |
0.613 |
|
| 2014 |
Majji G, Rout SK, Guin S, Gogoi A, Patel BK. Iodine-catalysed oxidative cyclisation of acylhydrazones to 2,5-substituted 1,3,4-oxadiazoles Rsc Advances. 4: 5357-5362. DOI: 10.1039/C3Ra44897E |
0.742 |
|
| 2014 |
Banerjee A, Bera A, Santra SK, Guin S, Patel BK. ChemInform Abstract: Palladium-Catalyzed Regioselective Aroylation and Acetoxylation of 3,5-Diarylisoxazole via ortho C-H Functionalizations. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201446162 |
0.616 |
|
| 2014 |
Khatun N, Guin S, Rout SK, Patel BK. ChemInform Abstract: Divergent Reactivities of O-Haloanilides with CuO Nanoparticles in Water: A Green Synthesis of Benzoxazoles and O-Hydroxyanilides. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201444131 |
0.704 |
|
| 2014 |
Majji G, Rout SK, Guin S, Gogoi A, Patel BK. ChemInform Abstract: Iodine-Catalyzed Oxidative Cyclization of Acylhydrazones to 2,5-Substituted 1,3,4-Oxadiazoles. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201440150 |
0.738 |
|
| 2014 |
Ali W, Guin S, Rout SK, Gogoi A, Patel BK. Thioesterification of Alkylbenzenes with ThiolsviaCopper- Catalyzed Cross-Dehydrogenative Coupling without a Directing Group Advanced Synthesis & Catalysis. 356: 3099-3105. DOI: 10.1002/Adsc.201400360 |
0.804 |
|
| 2014 |
Guin S, Rout SK, Gogoi A, Ali W, Patel BK. A palladium(II)-catalyzed synthesis of α-ketoamides via chemoselective aroyl addition to cyanamides Advanced Synthesis and Catalysis. 356: 2559-2565. DOI: 10.1002/Adsc.201400011 |
0.794 |
|
| 2013 |
Rout SK, Guin S, Banerjee A, Khatun N, Gogoi A, Patel BK. Directing group assisted copper-catalyzed chemoselective O-aroylation of phenols and enols using alkylbenzenes. Organic Letters. 15: 4106-9. PMID 23924444 DOI: 10.1021/Ol401682A |
0.753 |
|
| 2013 |
Gogoi A, Guin S, Rout SK, Patel BK. A copper-catalyzed synthesis of 3-aroylindoles via a sp3 C-H bond activation followed by C-C and C-O bond formation. Organic Letters. 15: 1802-5. PMID 23541283 DOI: 10.1021/Ol400692B |
0.79 |
|
| 2013 |
Majji G, Guin S, Gogoi A, Rout SK, Patel BK. Easy access to benzylic esters directly from alkyl benzenes under metal-free conditions. Chemical Communications (Cambridge, England). 49: 3031-3. PMID 23462810 DOI: 10.1039/C3Cc40832A |
0.754 |
|
| 2013 |
Banerjee A, Bera A, Guin S, Rout SK, Patel BK. Regioselective ortho-hydroxylation of 2-arylbenzothiazole via substrate directed C-H activation Tetrahedron. 69: 2175-2183. DOI: 10.1016/J.Tet.2012.12.067 |
0.779 |
|
| 2013 |
Banerjee A, Santra SK, Guin S, Rout SK, Patel BK. Palladium-catalyzed ortho-aroylation of 2-arylbenzothiazoles and 2-arylbenzoxazoles with aldehydes European Journal of Organic Chemistry. 1367-1376. DOI: 10.1002/Ejoc.201201503 |
0.8 |
|
| 2013 |
Banerjee A, Santra SK, Guin S, Rout SK, Patel BK. ChemInform Abstract: Palladium-Catalyzed ortho-Aroylation of 2-Arylbenzothiazoles and 2-Arylbenzoxazoles with Aldehydes. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201335127 |
0.773 |
|
| 2013 |
Banerjee A, Bera A, Guin S, Rout SK, Patel BK. ChemInform Abstract: Regioselective ortho-Hydroxylation of 2-Arylbenzothiazole via Substrate Directed C-H Activation. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201325123 |
0.754 |
|
| 2013 |
Guin S, Rout SK, Gogoi A, Nandi S, Ghara KK, Patel BK. ChemInform Abstract: Desulfurization Strategy in the Construction of Azoles Possessing Additional Nitrogen, Oxygen or Sulfur Using a Copper(I) Catalyst. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201312121 |
0.712 |
|
| 2013 |
Guin S, Rout SK, Khatun N, Ghosh T, Patel BK. ChemInform Abstract: Tandem Synthesis of [1,2,4]-Triazoles Mediated by Iodine - A Regioselective Approach. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201310144 |
0.732 |
|
| 2013 |
Rout SK, Guin S, Nath J, Patel BK. ChemInform Abstract: An “On-Water” Exploration of CuO Nanoparticle Catalyzed Synthesis of 2-Aminobenzothiazoles. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201302107 |
0.712 |
|
| 2012 |
Guin S, Rout SK, Banerjee A, Nandi S, Patel BK. Four tandem C-H activations: a sequential C-C and C-O bond making via a Pd-catalyzed cross dehydrogenative coupling (CDC) approach. Organic Letters. 14: 5294-7. PMID 23020217 DOI: 10.1021/Ol302438Z |
0.787 |
|
| 2012 |
Rout SK, Guin S, Ghara KK, Banerjee A, Patel BK. Copper catalyzed oxidative esterification of aldehydes with alkylbenzenes via cross dehydrogenative coupling. Organic Letters. 14: 3982-5. PMID 22817825 DOI: 10.1021/Ol301756Y |
0.772 |
|
| 2012 |
Guin S, Rout SK, Ghosh T, Khatun N, Patel BK. A one pot synthesis of [1,3,4]-oxadiazoles mediated by molecular iodine Rsc Advances. 2: 3180-3183. DOI: 10.1039/C2Ra00044J |
0.763 |
|
| 2012 |
Rout SK, Guin S, Nath J, Patel BK. An "on-water" exploration of CuO nanoparticle catalysed synthesis of 2-aminobenzothiazoles Green Chemistry. 14: 2491-2498. DOI: 10.1039/C2Gc35575B |
0.767 |
|
| 2012 |
Guin S, Rout SK, Khatun N, Ghosh T, Patel BK. Tandem synthesis of [1,2,4]-triazoles mediated by iodine - A regioselective approach Tetrahedron. 68: 5066-5074. DOI: 10.1016/J.Tet.2012.04.042 |
0.767 |
|
| 2012 |
Guin S, Rout SK, Ghosh T, Khatun N, Patel BK. ChemInform Abstract: A One-Pot Synthesis of [1,3,4]-Oxadiazoles Mediated by Molecular Iodine. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201231136 |
0.726 |
|
| 2012 |
Guin S, Rout SK, Gogoi A, Nandi S, Ghara KK, Patel BK. Desulfurization strategy in the construction of azoles possessing additional nitrogen, oxygen or sulfur using a copper(I) catalyst Advanced Synthesis and Catalysis. 354: 2757-2770. DOI: 10.1002/Adsc.201200408 |
0.767 |
|
| 2011 |
Guin S, Ghosh T, Rout SK, Banerjee A, Patel BK. Cu(II) catalyzed imine C-H functionalization leading to synthesis of 2,5-substituted 1,3,4-oxadiazoles. Organic Letters. 13: 5976-9. PMID 22007797 DOI: 10.1021/Ol202409R |
0.8 |
|
| 2010 |
Sahoo SK, Jamir L, Guin S, Patel BK. Copper(I)-Catalyzed Cascade Synthesis of 2-Arylsulfanyl- arylcyanamides Advanced Synthesis & Catalysis. 352: 2538-2548. DOI: 10.1002/Adsc.201000383 |
0.803 |
|
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