Soumitra Agasti - Publications

Affiliations: 
2018-2022 University of Manchester, Manchester, England, United Kingdom 

23 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
2023 Agasti S, Beltran F, Pye E, Kaltsoyannis N, Crisenza GEM, Procter DJ. A catalytic alkene insertion approach to bicyclo[2.1.1]hexane bioisosteres. Nature Chemistry. PMID 36781910 DOI: 10.1038/s41557-023-01135-y  0.649
2021 Péter Á, Agasti S, Knowles O, Pye E, Procter DJ. Recent advances in the chemistry of ketyl radicals. Chemical Society Reviews. 50: 5349-5365. PMID 33972956 DOI: 10.1039/d0cs00358a  0.783
2021 Agasti S, Beattie NA, McDouall JJW, Procter DJ. SmI-Catalyzed Intermolecular Coupling of Cyclopropyl Ketones and Alkynes: A Link between Ketone Conformation and Reactivity. Journal of the American Chemical Society. 143: 3655-3661. PMID 33629852 DOI: 10.1021/jacs.1c01356  0.578
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  0.805
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  0.789
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  0.77
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  0.676
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  0.829
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  0.793
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  0.662
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  0.719
2016 Dey A, Agasti S, Maiti D. Palladium catalysed meta-C-H functionalization reactions. Organic & Biomolecular Chemistry. PMID 27120353 DOI: 10.1039/C6Ob00395H  0.689
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  0.772
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  0.804
2015 Maity S, Agasti S, Earsad AM, Hazra A, Maiti D. Nickel-Catalyzed Insertion of Alkynes and Electron-Deficient Olefins into Unactivated sp(3) CH Bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 11320-4. PMID 26121618 DOI: 10.1002/Chem.201501962  0.806
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  0.831
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  0.54
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  0.803
2014 Deb A, Agasti S, Saboo T, Maiti D. ChemInform Abstract: Generation of Arylated Quinones by Iron-Catalyzed Oxidative Arylation of Phenols: Formal Synthesis of Phellodonin, Sarcodonin ε, Leucomelone and Betulinan A. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201434104  0.61
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  0.699
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  0.808
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  0.782
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  0.763
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