Rajesh Kancherla - Publications

Affiliations: 
2013-2016 Indian Institute of Technology Bombay, Mumbai, Maharashtra, India 

30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Karpova L, Daniel M, Kancherla R, Muralirajan K, Maity B, Rueping M. Excited-State Nickel-Catalyzed Amination of Aryl Bromides: Synthesis of Diphenylamines and Primary Anilines. Organic Letters. PMID 38381879 DOI: 10.1021/acs.orglett.4c00147  0.564
2023 Yi L, Zhu C, Chen X, Yue H, Ji T, Ma Y, Cao Y, Kancherla R, Rueping M. O-H bond activation of β,γ-unsaturated oximes hydrogen atom transfer (HAT) and photoredox dual catalysis. Chemical Science. 14: 14271-14279. PMID 38098711 DOI: 10.1039/d3sc04410f  0.557
2023 Kancherla R, Muralirajan K, Dutta S, Pal K, Li B, Maity B, Cavallo L, Rueping M. Photoexcitation of Distinct Divalent Palladium Complexes in Cross-Coupling Amination Under Air. Angewandte Chemie (International Ed. in English). e202314508. PMID 37956272 DOI: 10.1002/anie.202314508  0.73
2023 Muralirajan K, Kancherla R, Maity B, Karuthedath S, Laquai F, Cavallo L, Rueping M. Mechanistic insights into excited-state palladium catalysis for C-S bond formations and dehydrogenative sulfonylation of amines. Nature Communications. 14: 6622. PMID 37857662 DOI: 10.1038/s41467-023-42392-2  0.601
2023 Huang L, Szewczyk M, Kancherla R, Maity B, Zhu C, Cavallo L, Rueping M. Modulating stereoselectivity in allylic C(sp)-H bond arylations via nickel and photoredox catalysis. Nature Communications. 14: 548. PMID 36725849 DOI: 10.1038/s41467-023-36103-0  0.637
2022 Kumar GS, Shinde PS, Chen H, Muralirajan K, Kancherla R, Rueping M. Paired Electrolysis for Decarboxylative Cyanation: 4-CN-Pyridine, a Versatile Nitrile Source. Organic Letters. PMID 36036921 DOI: 10.1021/acs.orglett.2c01897  0.526
2022 Kancherla R, Muralirajan K, Rueping M. Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism. Chemical Science. 13: 8583-8589. PMID 35974758 DOI: 10.1039/d2sc02363f  0.541
2022 Kancherla R, Muralirajan K, Maity B, Karuthedath S, Kumar GS, Laquai F, Cavallo L, Rueping M. Mechanistic insights into photochemical nickel-catalyzed cross-couplings enabled by energy transfer. Nature Communications. 13: 2737. PMID 35585041 DOI: 10.1038/s41467-022-30278-8  0.533
2021 Muralirajan K, Kancherla R, Gimnkhan A, Rueping M. Unactivated Alkyl Chloride Reactivity in Excited-State Palladium Catalysis. Organic Letters. 23: 6905-6910. PMID 34432470 DOI: 10.1021/acs.orglett.1c02467  0.569
2020 Jia J, Kancherla R, Rueping M, Huang L. Allylic C(sp)-H alkylation synergistic organo- and photoredox catalyzed radical addition to imines. Chemical Science. 11: 4954-4959. PMID 34122952 DOI: 10.1039/d0sc00819b  0.658
2020 Jia J, Kancherla R, Rueping M, Huang L. Allylic C(sp3)–H alkylation via synergistic organo- and photoredox catalyzed radical addition to imines Chemical Science. 11: 4954-4959. DOI: 10.1039/D0Sc00819B  0.624
2020 Merkes JM, Lammers T, Kancherla R, Rueping M, Kiessling F, Banala S. Photoacoustic Imaging: Tuning Optical Properties of BODIPY Dyes by Pyrrole Conjugation for Photoacoustic Imaging (Advanced Optical Materials 11/2020) Advanced Optical Materials. 8: 2070046. DOI: 10.1002/Adom.202070046  0.423
2020 Merkes JM, Lammers T, Kancherla R, Rueping M, Kiessling F, Banala S. Tuning Optical Properties of BODIPY Dyes by Pyrrole Conjugation for Photoacoustic Imaging Advanced Optical Materials. 8: 1902115. DOI: 10.1002/Adom.201902115  0.455
2019 Huang L, Zhu C, Yi L, Yue H, Kancherla R, Rueping M. Cascade Cross-Coupling of Dienes: Photoredox and Nickel Dual Catalysis. Angewandte Chemie (International Ed. in English). PMID 31778289 DOI: 10.1002/Anie.201911109  0.607
2019 Kancherla R, Muralirajan K, Maity B, Zhu C, Krach PE, Cavallo L, Rueping M. Cover Picture: Oxidative Addition to Palladium(0) Made Easy through Photoexcited-State Metal Catalysis: Experiment and Computation (Angew. Chem. Int. Ed. 11/2019) Angewandte Chemie International Edition. 58: 3229-3229. DOI: 10.1002/Anie.201900572  0.479
2019 Kancherla R, Muralirajan K, Maity B, Zhu C, Krach PE, Cavallo L, Rueping M. Titelbild: Oxidative Addition to Palladium(0) Made Easy through Photoexcited-State Metal Catalysis: Experiment and Computation (Angew. Chem. 11/2019) Angewandte Chemie. 131: 3263-3263. DOI: 10.1002/Ange.201900572  0.479
2018 Kancherla R, Muralirajan K, Maity B, Zhu C, Krach PE, Cavallo L, Rueping M. Oxidative Addition to Palladium(0) Made Easy through Photoexcited-State Metal Catalysis: Experiment and Computation. Angewandte Chemie (International Ed. in English). PMID 30520235 DOI: 10.1002/Anie.201811439  0.592
2018 Muralirajan K, Kancherla R, Rueping M. Dehydrogenative Aromatization and Sulfonylation of Pyrrolidines: Orthogonal Reactivity in Photoredox Catalysis. Angewandte Chemie (International Ed. in English). PMID 30307106 DOI: 10.1002/Anie.201808427  0.581
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  0.791
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  0.743
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  0.791
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  0.694
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  0.77
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  0.796
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  0.777
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  0.78
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  0.817
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  0.837
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  0.755
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  0.746
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