Rajendr Thakuri - Related publications

Affiliations: 
2013-2020 Chemistry and Biochemistry University of Toledo, Toledo, OH, United States 
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30 most relevant papers in past 60 days:
Year Citation  Score
2022 Liao G, Zhang T, Jin L, Wang BJ, Xu CK, Lan Y, Zhao Y, Shi BF. Experimental and Computational Studies on the Directing Ability of Chalcogenoethers in Palladium-Catalyzed Atroposelective C-H Olefination and Allylation. Angewandte Chemie (International Ed. in English). PMID 34985788 DOI: 10.1002/anie.202115221   
2022 Nie FY, Cai YP, Song QH. Visible Light-Driven Decarboxylative Alkylation of Aldehydes via Electron Donor-Acceptor Complexes of Active Esters. The Journal of Organic Chemistry. PMID 34989227 DOI: 10.1021/acs.joc.1c02586   
2022 Yang P, Wang Q, Cui BH, Zhang XD, Liu H, Zhang YY, Liu JL, Huang WY, Liang RX, Jia YX. Enantioselective Dearomative [3 + 2] Umpolung Annulation of -Heteroarenes with Alkynes. Journal of the American Chemical Society. PMID 35007081 DOI: 10.1021/jacs.1c11092   
2022 Min XL, Zhang XL, Yi W, He Y. Brønsted acid-enhanced copper-catalyzed atroposelective cycloisomerization to axially chiral arylquinolizones via dearomatization of pyridine. Nature Communications. 13: 373. PMID 35042873 DOI: 10.1038/s41467-022-27989-3   
2022 Mahato S, Rawal P, Devadkar AK, Joshi M, Roy Choudhury A, Biswas B, Gupta P, Panda TK. Hydroboration and reductive amination of ketones and aldehydes with HBpin by a bench stable Pd(II)-catalyst. Organic & Biomolecular Chemistry. PMID 35029621 DOI: 10.1039/d1ob02339j   
2022 Karandikar SS, Stuart DR. Refining boron-iodane exchange to access versatile arylation reagents. Chemical Communications (Cambridge, England). 58: 1211-1214. PMID 34982811 DOI: 10.1039/d1cc06341c   
2022 Shiomi S, Shennan BDA, Yamazaki K, Fuentes de Arriba ÁL, Vasu D, Hamlin TA, Dixon DJ. A New Organocatalytic Desymmetrization Reaction Enables the Enantioselective Total Synthesis of Madangamine E. Journal of the American Chemical Society. PMID 35037758 DOI: 10.1021/jacs.1c12040   
2022 Ren W, Wang M, Guo J, Zhou J, Chu J, Shi Y, Shi Y. Pd-Catalyzed Regioselective Branched Hydrocarboxylation of Terminal Olefins with Formic Acid. Organic Letters. PMID 35029395 DOI: 10.1021/acs.orglett.1c04231   
2022 Yan JL, Maiti R, Ren SC, Tian W, Li T, Xu J, Mondal B, Jin Z, Chi YR. Carbene-catalyzed atroposelective synthesis of axially chiral styrenes. Nature Communications. 13: 84. PMID 35013298 DOI: 10.1038/s41467-021-27771-x   
2022 Li Z, Xu R, Guo H, Yang H, Xu G, Shi E, Xiao J, Tang W. Enantioselective Rhodium-Catalyzed Hydrogenation of ()--Sulfonyl-α-dehydroamido Boronic Esters. Organic Letters. PMID 34978454 DOI: 10.1021/acs.orglett.1c04157   
2022 Yoon H, Galls A, Rozema SD, Miller SJ. Atroposelective Desymmetrization of Resorcinol-Bearing Quinazolinones via Cu-Catalyzed C-O Bond Formation. Organic Letters. PMID 35007090 DOI: 10.1021/acs.orglett.1c04266   
2022 Forson KG, Bohman BO, Wayment CZ, Owens RN, McKnight CE, Davis RC, Stillwell LR, Smith SJ, Michaelis DJ. Medium and Large -Heterocycle Formation via Allene Hydroamination with a Bimetallic Rh(II) Catalyst. Journal of the American Chemical Society. 144: 63-68. PMID 34965105 DOI: 10.1021/jacs.1c10534   
2022 Panda TK, Kumar R, Rawal P, Banerjee I, Nayek HP, Gupta P, Panda TK. Catalytic Hydroboration and Reductive Amination of Carbonyl Compounds by HBpin using a Zinc Promoter. Chemistry, An Asian Journal. PMID 35020275 DOI: 10.1002/asia.202200013   
2022 Kariofillis SK, Jiang S, Żurański AM, Gandhi SS, Martinez Alvarado JI, Doyle AG. Using Data Science To Guide Aryl Bromide Substrate Scope Analysis in a Ni/Photoredox-Catalyzed Cross-Coupling with Acetals as Alcohol-Derived Radical Sources. Journal of the American Chemical Society. PMID 34985904 DOI: 10.1021/jacs.1c12203   
2022 Dasgupta A, Richards E, Melen RL. Triarylborane Catalyzed Carbene Transfer Reactions Using Diazo Precursors. Acs Catalysis. 12: 442-452. PMID 35028191 DOI: 10.1021/acscatal.1c04746   
2022 Chen K, Kang QK, Li Y, Wu WQ, Zhu H, Shi H. Catalytic Amination of Phenols with Amines. Journal of the American Chemical Society. PMID 35015956 DOI: 10.1021/jacs.1c12622   
2022 Zou W, Gao L, Cao J, Li Z, Li G, Wang G, Li S. Mechanistic Insight into Hydroboration of Imines from Combined Computational and Experimental Studies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35018677 DOI: 10.1002/chem.202104004   
2022 Sun SZ, Cai YM, Zhang DL, Wang JB, Yao HQ, Rui XY, Martin R, Shang M. Enantioselective Deaminative Alkylation of Amino Acid Derivatives with Unactivated Olefins. Journal of the American Chemical Society. PMID 35029378 DOI: 10.1021/jacs.1c12350   
2022 Alomari K, Sai Pavan Chakravarthy N, Duchadeau B, Ermanis K, Clarke PA. Enantioselective "clip-cycle" synthesis of di-, tri- and spiro-substituted tetrahydropyrans. Organic & Biomolecular Chemistry. PMID 35044408 DOI: 10.1039/d2ob00023g   
2022 Li B, Xu H, Dang Y, Houk KN. Dispersion and Steric Effects on Enantio-/Diastereoselectivities in Synergistic Dual Transition-Metal Catalysis. Journal of the American Chemical Society. PMID 35049279 DOI: 10.1021/jacs.1c12664   
2022 Zhang WW, Liu CX, Yang P, Zhang SZ, Gu Q, You SL. Rhodium-Catalyzed Atroposelective C-H/C-H Cross-Coupling Reaction between 1-Aryl Isoquinoline Derivatives and Indolizines. Organic Letters. PMID 34985290 DOI: 10.1021/acs.orglett.1c04002   
2022 Estaitie M, Hall DG. Regiocontrolled synthesis of enantioenriched 2-substituted dehydropiperidines by stereospecific allyl-allyl cross-coupling of a chiral allylic boronate. Chemical Communications (Cambridge, England). PMID 34989368 DOI: 10.1039/d1cc06186k   
2022 Natarajan M, Kumar N, Joshi M, Stein M, Kaur-Ghumaan S. Mechanism of Diiron Hydrogenase Complexes Controlled by Nature of Bridging Dithiolate Ligand. Chemistryopen. 11: e202100238. PMID 34981908 DOI: 10.1002/open.202100238   
2022 Tu Y, Yang JS, Lu K, Li CX, Zhao ZH, Zhang XM, Zhang FM. Chiral 1,2,3-Triazolium Salt Catalyzed Asymmetric Mono- and Dialkylation of 2,5-Diketopiperazines with the Construction of Tetrasubstituted Carbon Centers. Angewandte Chemie (International Ed. in English). PMID 34981881 DOI: 10.1002/anie.202114129   
2022 Smedley CJ, Homer JA, Gialelis TL, Barrow AS, Koelln RA, Moses JE. Accelerated SuFEx Click Chemistry For Modular Synthesis. Angewandte Chemie (International Ed. in English). 61: e202112375. PMID 34755436 DOI: 10.1002/anie.202112375   
2022 Lei L, Zou PS, Wang ZX, Liang C, Hou C, Mo DL. Palladacycle-Catalyzed Regioselective Heck Reaction Using Diaryliodonium Triflates and Aryl Iodides. Organic Letters. PMID 34995468 DOI: 10.1021/acs.orglett.1c04120   
2022 Yin C, Pan Y, Zhang X, Yin Q. Catalytic Asymmetric Hydrogenation of Tetrasubstituted Unsaturated Lactams: An Efficient Approach to Enantioenriched 3,4-Disubstituted Piperidines. Organic Letters. 24: 675-680. PMID 35005963 DOI: 10.1021/acs.orglett.1c04132   
2022 Rozsar D, Formica M, Yamazaki K, Hamlin TA, Dixon DJ. Bifunctional Iminophosphorane-Catalyzed Enantioselective Sulfa-Michael Addition to Unactivated α,β-Unsaturated Amides. Journal of the American Chemical Society. PMID 34990142 DOI: 10.1021/jacs.1c11898   
2022 Ding H, Gao W, Yu T, Wang Z, Gou F, Ding S. Hydroboration and Diboration of Internal Alkynes under Iridium Catalysis. The Journal of Organic Chemistry. PMID 34995462 DOI: 10.1021/acs.joc.1c02315   
2022 Lou Y, Wei J, Li M, Zhu Y. Distal Ionic Substrate-Catalyst Interactions Enable Long-Range Stereocontrol: Access to Remote Quaternary Stereocenters through a Desymmetrizing Suzuki-Miyaura Reaction. Journal of the American Chemical Society. PMID 34979078 DOI: 10.1021/jacs.1c12345