Year |
Citation |
Score |
2023 |
Luo Y, Li Y, Wu J, Xue XS, Hartwig JF, Shen Q. Oxidative addition of an alkyl halide to form a stable Cu(III) product. Science (New York, N.Y.). 381: 1072-1079. PMID 37676952 DOI: 10.1126/science.adg9232 |
0.457 |
|
2023 |
Jiang W, Huang W, Xu M, Leng X, Lu L, Shen Q. Diimidazolium Salt HBDIM: An Easily Available, Low-Cost CageCarbene Precursor with Broad Applications in Transition Metal-Catalyzed Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). e202300991. PMID 37143186 DOI: 10.1002/chem.202300991 |
0.561 |
|
2023 |
Liu J, Xiao Y, Hao J, Shen Q. Copper-Catalyzed Trifluoromethylation of (Hetero)aryl Boronic Acid Pinacol Esters with YlideFluor. Organic Letters. PMID 36779647 DOI: 10.1021/acs.orglett.3c00206 |
0.38 |
|
2022 |
Zhao H, Leng X, Zhang W, Shen Q. [Ph4P]+[Cu(CF2H)2]-: A Powerful Difluoromethylating Reagent Inspired by Mechanistic Investigation. Angewandte Chemie (International Ed. in English). PMID 36031582 DOI: 10.1002/anie.202210151 |
0.342 |
|
2021 |
Zhao H, Lu C, Herbert S, Zhang W, Shen Q. Difluoromethylation of Alkyl Bromides and Iodides with TMSCFH. The Journal of Organic Chemistry. PMID 33464896 DOI: 10.1021/acs.joc.0c02783 |
0.322 |
|
2020 |
Shen F, Lu L, Shen Q. Electrophilic fluoroalkylthiolation induced diastereoselective and stereospecific 1,2-metalate migration of alkenylboronate complexes. Chemical Science. 11: 8020-8024. PMID 34123079 DOI: 10.1039/d0sc03039b |
0.529 |
|
2020 |
Huang W, Wan X, Shen Q. Cobalt-Catalyzed Asymmetric Cross-Coupling Reaction of Fluorinated Secondary Benzyl Bromides with Lithium Aryl Boronates/ZnBr. Organic Letters. PMID 32432476 DOI: 10.1021/Acs.Orglett.0C01363 |
0.498 |
|
2020 |
Liu S, Liu H, Liu S, Zehai L, Lu C, Leng X, Lan Y, Shen Q. C(sp)-CF Reductive Elimination from a Five-Coordinate Neutral Copper(III) Complex. Journal of the American Chemical Society. PMID 32365294 DOI: 10.1021/Jacs.0C03304 |
0.346 |
|
2020 |
Zhao H, Herbert S, Kinzel T, Zhang W, Shen Q. Two ligands transfer from Ag to Pd: En Route to (SIPr)Pd(CF2H)(X) and its Application in One-pot C-H Borylation/Difluoromethylation. The Journal of Organic Chemistry. PMID 31970986 DOI: 10.1021/Acs.Joc.9B03296 |
0.351 |
|
2020 |
Shen F, Lu L, Shen Q. Electrophilic fluoroalkylthiolation induced diastereoselective and stereospecific 1,2-metalate migration of alkenylboronate complexes Chemical Science. 11: 8020-8024. DOI: 10.1039/D0Sc03039B |
0.576 |
|
2020 |
Zhao Q, Yao R, Chen W, Lu L, Shen Q. Scalable Synthesis of S-Fluoromethyl Benzenesulfonothioate Organic Process Research & Development. 24: 1090-1094. DOI: 10.1021/Acs.Oprd.0C00101 |
0.562 |
|
2020 |
Hong X, Liu Y, Lu L, Shen Q. Monofluoromethyl‐Substituted Sulfonium Ylides: Preparation, Structure‐Reactivity Study and Substrate Scope Chinese Journal of Chemistry. DOI: 10.1002/Cjoc.202000206 |
0.56 |
|
2019 |
Shen F, Zheng H, Xue XS, Lu L, Shen Q. Transition-Metal-Free -Trifluoromethylthiolation of Lithium Aryl Boronates. Organic Letters. PMID 31373823 DOI: 10.1021/Acs.Orglett.9B02236 |
0.583 |
|
2019 |
Huang W, Hu M, Wan X, Shen Q. Facilitating the transmetalation step with aryl-zincates in nickel-catalyzed enantioselective arylation of secondary benzylic halides. Nature Communications. 10: 2963. PMID 31273211 DOI: 10.1038/S41467-019-10851-4 |
0.488 |
|
2019 |
Lu Z, Liu H, Liu S, Leng X, Lan Y, Shen Q. Key Intermediate in Copper-Mediated Arene Trifluoromethylation [nBu4N][Cu(Ar)(CF3)3]: Synthesis, Characterization and C(sp2)-CF3 Reductive Elimination. Angewandte Chemie (International Ed. in English). PMID 31004379 DOI: 10.1002/Anie.201904041 |
0.357 |
|
2019 |
Liu Y, Ge H, Lu L, Shen Q. Pentafluoroethyl-Substituted Sulfonium Ylides: New Electrophilic Pentafluoroethylating Reagents Chinese Journal of Organic Chemistry. 39: 257. DOI: 10.6023/Cjoc201807018 |
0.37 |
|
2019 |
Hong X, Lu L, Shen Q. Copper-Catalyzed Carbene Insertion into the Sulfur–Sulfur Bond of RS–SCF2H/SCF3 under Mild Conditions Synlett. 30: 1602-1606. DOI: 10.1055/S-0037-1611839 |
0.605 |
|
2019 |
Liu S, Huang W, Wang D, Wei P, Shen Q. Cobalt-catalyzed cross-coupling of lithium (hetero)aryl zincates with heteroaryl chlorides and bromides Organic Chemistry Frontiers. 6: 2630-2634. DOI: 10.1039/C9Qo00551J |
0.481 |
|
2019 |
Liu H, Shen Q. Bistrifluoromethylated organocuprate [Ph4P]+[Cu(CF3)2]−: synthesis, characterization and its application for trifluoromethylation of activated heteroaryl bromides, chlorides and iodides Organic Chemistry Frontiers. 6: 2324-2328. DOI: 10.1039/C9Qo00527G |
0.35 |
|
2019 |
Chen D, Lu L, Shen Q. [Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates Organic Chemistry Frontiers. 6: 1801-1806. DOI: 10.1039/C9Qo00278B |
0.385 |
|
2019 |
Ge H, Shen Q. Trifluoromethyl-substituted selenium ylide: a broadly applicable electrophilic trifluoromethylating reagent Organic Chemistry Frontiers. 6: 2205-2209. DOI: 10.1039/C8Qo01249K |
0.428 |
|
2019 |
Shao X, Hong X, Lu L, Shen Q. Cobalt-catalyzed hydro-difluoromethylthiolation/hydro-trifluoromethylthiolation of unactivated alkenes Tetrahedron. 75: 4156-4166. DOI: 10.1016/J.Tet.2019.05.061 |
0.652 |
|
2018 |
Wu J, Zhao Q, Wilson T, Verhoog S, Gouverneur V, Lu L, Shen Q. Synthesis and Reactivity of α-Cumyl bromodifluoromethanesulfenate: Application to the Radiosynthesis of [18F]arylSCF3. Angewandte Chemie (International Ed. in English). PMID 30575245 DOI: 10.1002/Anie.201813708 |
0.615 |
|
2018 |
Xu B, Li D, Lu L, Wang D, Hu Y, Shen Q. Radical fluoroalkylthiolation of aldehydes with PhSO2SRf (Rf = CF3, C2F5, CF2H or CH2F): a general protocol for the preparation of fluoroalkylthioesters Organic Chemistry Frontiers. 5: 2163-2166. DOI: 10.1039/C8Qo00327K |
0.441 |
|
2018 |
Xu B, Wang D, Hu Y, Shen Q. Silver-catalyzed ring-opening difluoromethylthiolation/trifluoromethylthiolation of cycloalkanols with PhSO2SCF2H or PhSO2SCF3 Organic Chemistry Frontiers. 5: 1462-1465. DOI: 10.1039/C8Qo00115D |
0.379 |
|
2018 |
Liu S, Kang K, Liu S, Wang D, Wei P, Lan Y, Shen Q. The Difluoromethylated Organogold(III) Complex cis-[Au(PCy3)(4-F-C6H4)(CF2H)(Cl)]: Preparation, Characterization, and Its C(sp2)–CF2H Reductive Elimination Organometallics. 37: 3901-3908. DOI: 10.1021/Acs.Organomet.8B00579 |
0.323 |
|
2018 |
Wu J, Lu C, Lu L, Shen Q. Pd-Catalyzed Difluoromethylthiolation of Aryl Chlorides, Bromides and Triflates Chinese Journal of Chemistry. 36: 1031-1034. DOI: 10.1002/Cjoc.201800306 |
0.55 |
|
2017 |
Lu C, Lu H, Wu J, Shen HC, Hu T, Gu Y, Shen Q. Palladium-Catalyzed Difluoromethylation of Aryl Chlorides and Triflates and Its Applications in the Preparation of Difluoromethylated Derivatives of Drug/Agrochemical Molecules. The Journal of Organic Chemistry. PMID 29271195 DOI: 10.1021/Acs.Joc.7B02989 |
0.386 |
|
2017 |
Lu C, Gu Y, Wu J, Gu Y, Shen Q. Palladium-catalyzed difluoromethylation of heteroaryl chlorides, bromides and iodides. Chemical Science. 8: 4848-4852. PMID 28959407 DOI: 10.1039/C7Sc00691H |
0.449 |
|
2017 |
Huang W, Wan X, Shen Q. Enantioselective Construction of Trifluoromethoxylated Stereogenic Centers by Nickel-Catalyzed Asymmetric Suzuki-Miyaura Coupling of Secondary Benzyl Bromides. Angewandte Chemie (International Ed. in English). PMID 28726345 DOI: 10.1002/Anie.201706868 |
0.493 |
|
2017 |
Zhao Q, Lu L, Shen Q. Direct Monofluoromethylthiolation with S-(fluoromethyl) benzenesulfonothioate. Angewandte Chemie (International Ed. in English). PMID 28688163 DOI: 10.1002/Anie.201705633 |
0.638 |
|
2017 |
Liu Y, Lu L, Shen Q. Monofluoromethyl-Substituted Sulfonium Ylides: Electrophilic Monofluoromethylating Reagents with Broad Substrate Scopes. Angewandte Chemie (International Ed. in English). PMID 28544561 DOI: 10.1002/Anie.201704175 |
0.618 |
|
2017 |
Shen F, Zhang P, Lu L, Shen Q. [[(Ethoxycarbonyl)difluoromethyl]thio]phthalimide: A Shelf-Stable, Electrophilic Reagent with a Convertible Group for the Synthesis of Diversified Fluoroalkylthiolated Compounds. Organic Letters. PMID 28198189 DOI: 10.1021/Acs.Orglett.7B00010 |
0.58 |
|
2017 |
Zhang H, Leng X, Wan X, Shen Q. (1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation Organic Chemistry Frontiers. 4: 1051-1057. DOI: 10.1039/C7Qo00042A |
0.312 |
|
2017 |
Zhu D, Hong X, Li D, Lu L, Shen Q. A Two-Step, One-Pot, and Multigram-Scale Synthesis of N-Difluoromethylthiophthalimide Organic Process Research & Development. 21: 1383-1387. DOI: 10.1021/Acs.Oprd.7B00203 |
0.77 |
|
2017 |
Gu Y, Lu C, Gu Y, Shen Q. Ligand-Controlled Copper-Catalyzed Highly Regioselective Difluoromethylation of Allylic Chlorides/Bromides and Propargyl Bromides Chinese Journal of Chemistry. 36: 55-58. DOI: 10.1002/Cjoc.201700594 |
0.387 |
|
2017 |
Zhu J, Xu C, Xu C, Shen Q. Preparation of N-Trifluoromethylthiosaccharin: A Shelf-Stable Electrophilic Reagent for Trifluoromethylthiolation Organic Syntheses. 94: 217-233. DOI: 10.1002/0471264229.Os094.16 |
0.32 |
|
2016 |
Wu J, Liu Y, Lu C, Shen Q. Palladium-catalyzed difluoromethylthiolation of heteroaryl bromides, iodides, triflates and aryl iodides. Chemical Science. 7: 3757-3762. PMID 29997863 DOI: 10.1039/C6Sc00082G |
0.462 |
|
2016 |
Zhu D, Shao X, Hong X, Lu L, Shen Q. PhSO2 SCF2 H: A Shelf-Stable, Easily Scalable Reagent for Radical Difluoromethylthiolation. Angewandte Chemie (International Ed. in English). PMID 27860002 DOI: 10.1002/Anie.201609468 |
0.787 |
|
2016 |
Zhang P, Li M, Xue XS, Xu C, Zhao Q, Liu Y, Wang H, Guo Y, Lu L, Shen Q. N-Trifluoromethylthiodibenzenesulfonimide: A Shelf-Stable, Broadly Applicable Electrophilic Trifluoromethylthiolating Reagent. The Journal of Organic Chemistry. PMID 27441822 DOI: 10.1021/Acs.Joc.6B01178 |
0.616 |
|
2016 |
Zhu J, Liu Y, Shen Q. Direct Difluoromethylation of Alcohols with an Electrophilic Difluoromethylated Sulfonium Ylide. Angewandte Chemie (International Ed. in English). PMID 27312192 DOI: 10.1002/Anie.201603166 |
0.456 |
|
2016 |
Zhu J, Li Y, Ni C, Shen Q. Pentafluoroethylbenziodoxole (BIX-C2F5): A Shelf-Stable Reagent for Pentafluoroethylation of β-Ketoesters and Arylboronic Acids Chinese Journal of Chemistry. 34: 662-668. DOI: 10.1002/Cjoc.201600097 |
0.398 |
|
2015 |
Xu C, Shen Q. Lewis Acid Mediated Trifluoromethylthio Lactonization/Lactamization. Organic Letters. 17: 4561-3. PMID 26352922 DOI: 10.1021/Acs.Orglett.5B02315 |
0.407 |
|
2015 |
Zhu D, Gu Y, Lu L, Shen Q. N-Difluoromethylthiophthalimide: A Shelf-Stable, Electrophilic Reagent for Difluoromethylthiolation. Journal of the American Chemical Society. PMID 26178409 DOI: 10.1021/Jacs.5B03170 |
0.793 |
|
2015 |
Liu Y, Shao X, Zhang P, Lu L, Shen Q. Trifluoromethyl-substituted sulfonium ylide: rh-catalyzed carbenoid addition to trifluoromethylthioether. Organic Letters. 17: 2752-5. PMID 25974253 DOI: 10.1021/Acs.Orglett.5B01170 |
0.66 |
|
2015 |
Wu J, Gu Y, Leng X, Shen Q. Copper-Promoted Sandmeyer Difluoromethylthiolation of Aryl and Heteroaryl Diazonium Salts. Angewandte Chemie (International Ed. in English). 54: 7648-52. PMID 25967113 DOI: 10.1002/Anie.201502113 |
0.482 |
|
2015 |
Shao X, Xu C, Lu L, Shen Q. Shelf-stable electrophilic reagents for trifluoromethylthiolation. Accounts of Chemical Research. 48: 1227-36. PMID 25947041 DOI: 10.1021/Acs.Accounts.5B00047 |
0.643 |
|
2015 |
Sun Q, Wang Y, Yuan D, Yao Y, Shen Q. Zirconium catalysed intermolecular hydroamination reactions of secondary amines with alkynes. Chemical Communications (Cambridge, England). 51: 7633-6. PMID 25847386 DOI: 10.1039/c5cc01780g |
0.35 |
|
2015 |
Wiggins KM, Hudnall TW, Shen Q, Kryger MJ, Moore JS, Bielawski CW. Retraction of "Mechanical reconfiguration of stereoisomers". Journal of the American Chemical Society. 137: 3428. PMID 25758672 DOI: 10.1021/Jacs.5B01988 |
0.719 |
|
2015 |
Chang D, Gu Y, Shen Q. Pd-catalyzed difluoromethylation of vinyl bromides, triflates, tosylates, and nonaflates. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 6074-8. PMID 25752832 DOI: 10.1002/Chem.201500551 |
0.422 |
|
2015 |
Shao X, Xu C, Lu L, Shen Q. Structure-reactivity relationship of trifluoromethanesulfenates: discovery of an electrophilic trifluoromethylthiolating reagent. The Journal of Organic Chemistry. 80: 3012-21. PMID 25621904 DOI: 10.1021/Jo502645M |
0.648 |
|
2015 |
Yang T, Lu L, Shen Q. Iron-mediated Markovnikov-selective hydro-trifluoromethylthiolation of unactivated alkenes. Chemical Communications (Cambridge, England). 51: 5479-81. PMID 25487645 DOI: 10.1039/C4Cc08655D |
0.608 |
|
2015 |
Gu Y, Chang D, Leng X, Shen Q. Well-Defined, Shelf-Stable (NHC)Ag(CF2H) Complexes for Difluoromethylation Organometallics. 34: 3065-3071. DOI: 10.1021/Acs.Organomet.5B00350 |
0.368 |
|
2015 |
Ma B, Shao X, Shen Q. BrØsted acid-catalyzed electrophilic trifluoromethylthiolation of indoles using thermally stable trifluoromethylthiolating reagent Journal of Fluorine Chemistry. 171: 73-77. DOI: 10.1016/J.Jfluchem.2014.09.011 |
0.471 |
|
2014 |
Gu Y, Leng X, Shen Q. Cooperative dual palladium/silver catalyst for direct difluoromethylation of aryl bromides and iodides. Nature Communications. 5: 5405. PMID 25377759 DOI: 10.1038/Ncomms6405 |
0.436 |
|
2014 |
Yu D, Wang CS, Yao C, Shen Q, Lu L. Nickel-catalyzed α-arylation of zinc enolates with polyfluoroarenes via C-F bond activation under neutral conditions. Organic Letters. 16: 5544-7. PMID 25321322 DOI: 10.1021/Ol502499Q |
0.621 |
|
2014 |
Shao X, Liu T, Lu L, Shen Q. Copper-catalyzed trifluoromethylthiolation of primary and secondary alkylboronic acids. Organic Letters. 16: 4738-41. PMID 25198142 DOI: 10.1021/Ol502132J |
0.776 |
|
2014 |
Xu C, Ma B, Shen Q. N-trifluoromethylthiosaccharin: an easily accessible, shelf-stable, broadly applicable trifluoromethylthiolating reagent. Angewandte Chemie (International Ed. in English). 53: 9316-20. PMID 25045031 DOI: 10.1002/Anie.201403983 |
0.414 |
|
2014 |
Hu F, Shao X, Zhu D, Lu L, Shen Q. Silver-catalyzed decarboxylative trifluoromethylthiolation of aliphatic carboxylic acids in aqueous emulsion. Angewandte Chemie (International Ed. in English). 53: 6105-9. PMID 24764209 DOI: 10.1002/Anie.201402573 |
0.789 |
|
2014 |
Xu C, Shen Q. Palladium-catalyzed trifluoromethylthiolation of aryl C-H bonds. Organic Letters. 16: 2046-9. PMID 24661053 DOI: 10.1021/Ol5006533 |
0.381 |
|
2014 |
Kang K, Xu C, Shen Q. Copper-catalyzed trifluoromethylthiolation of aryl and vinyl boronic acids with a shelf-stable electrophilic trifluoromethylthiolating reagent Organic Chemistry Frontiers. 1: 294-297. DOI: 10.1039/C3Qo00068K |
0.512 |
|
2014 |
Yang T, Shen Q, Lu L. Chincona Alkaloid‐Catalyzed Enantioselective Trifluoromethylthiolation of Oxindoles Chinese Journal of Chemistry. 32: 678-680. DOI: 10.1002/Cjoc.201400392 |
0.669 |
|
2013 |
Wang X, Yang T, Cheng X, Shen Q. Enantioselective electrophilic trifluoromethylthiolation of β-ketoesters: a case of reactivity and selectivity bias for organocatalysis. Angewandte Chemie (International Ed. in English). 52: 12860-4. PMID 24000200 DOI: 10.1002/Anie.201305075 |
0.605 |
|
2013 |
Yu D, Lu L, Shen Q. Palladium-catalyzed coupling of polyfluorinated arenes with heteroarenes via C-F/C-H activation. Organic Letters. 15: 940-3. PMID 23391131 DOI: 10.1021/Ol303567T |
0.559 |
|
2013 |
Shao X, Wang X, Yang T, Lu L, Shen Q. An electrophilic hypervalent iodine reagent for trifluoromethylthiolation. Angewandte Chemie (International Ed. in English). 52: 3457-60. PMID 23355233 DOI: 10.1002/Anie.201209817 |
0.612 |
|
2013 |
Wen L, Yin L, Shen Q, Lu L. Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to β-Trifluoromethylated Acrylamides Acs Catalysis. 3: 502-506. DOI: 10.1021/Cs300806W |
0.633 |
|
2013 |
Chen S, Xu C, Lu L, Shen Q. Cover Picture: Palladium-Catalyzed Cross-Coupling of Fluorinated Vinyl Chlorides with Terminal Alkynes: A General Protocol to Fluorinated Enynes (Chin. J. Chem. 7/2013) Chinese Journal of Chemistry. 31: 865-865. DOI: 10.1002/Cjoc.201390016 |
0.6 |
|
2013 |
Chen S, Xu C, Lu L, Shen Q. Palladium-Catalyzed Cross-Coupling of Fluorinated Vinyl Chlorides with Terminal Alkynes: A General Protocol to Fluorinated Enynes Chinese Journal of Chemistry. 31: 901-907. DOI: 10.1002/Cjoc.201300352 |
0.611 |
|
2013 |
Wang L, Shen Q, Lu L. A General and Highly Selective Method for the Asymmetric Synthesis of Trifluoromethyl-Substituted alpha- and beta-Aminophosphonates Chinese Journal of Chemistry. 31: 892-900. DOI: 10.1002/Cjoc.201300344 |
0.622 |
|
2013 |
Shao X, Wang X, Yang T, Lu L, Shen Q. Back Cover: An Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation (Angew. Chem. Int. Ed. 12/2013) Angewandte Chemie International Edition. 52: 3534-3534. DOI: 10.1002/Anie.201301409 |
0.663 |
|
2013 |
Shao X, Wang X, Yang T, Lu L, Shen Q. Rücktitelbild: An Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation (Angew. Chem. 12/2013) Angewandte Chemie. 125: 3620-3620. DOI: 10.1002/Ange.201301409 |
0.717 |
|
2012 |
Xu C, Chen S, Lu L, Shen Q. Preparation of trifluorostyrenes via palladium-catalyzed coupling of arylboronic acids with chloro- and bromotrifluoroethylene. The Journal of Organic Chemistry. 77: 10314-20. PMID 23078023 DOI: 10.1021/Jo301998G |
0.58 |
|
2012 |
Hu Z, Li Y, Liu K, Shen Q. Bis(perfluoroalkyl) phosphino-oxazoline: a modular, stable, strongly π-accepting ligand for asymmetric catalysis. The Journal of Organic Chemistry. 77: 7957-67. PMID 22924687 DOI: 10.1021/Jo3011717 |
0.372 |
|
2012 |
Qi Q, Shen Q, Lu L. Copper-mediated aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides at room temperature. Journal of the American Chemical Society. 134: 6548-51. PMID 22458339 DOI: 10.1021/Ja301705Z |
0.583 |
|
2012 |
Yu D, Shen Q, Lu L. Selective palladium-catalyzed C-F activation/carbon-carbon bond formation of polyfluoroaryl oxazolines. The Journal of Organic Chemistry. 77: 1798-804. PMID 22283549 DOI: 10.1021/Jo2023262 |
0.647 |
|
2012 |
Liu T, Shao X, Wu Y, Shen Q. Highly selective trifluoromethylation of 1,3-disubstituted arenes through iridium-catalyzed arene borylation. Angewandte Chemie (International Ed. in English). 51: 540-3. PMID 22128037 DOI: 10.1002/Anie.201106673 |
0.768 |
|
2012 |
Liu T, Zhao X, Shen Q, Lu L. General and highly efficient fluorinated-N-heterocyclic carbene–based catalysts for the palladium-catalyzed Suzuki–Miyaura reaction Tetrahedron. 68: 6535-6547. DOI: 10.1016/J.Tet.2012.05.068 |
0.65 |
|
2012 |
Wen L, Zhang H, Lin H, Shen Q, Lu L. A facile synthetic route to 2-trifluoromethyl-substituted polyfunctionalized chromenes and chromones Journal of Fluorine Chemistry. 133: 171-177. DOI: 10.1016/J.Jfluchem.2011.10.011 |
0.595 |
|
2012 |
Qi Q, Shen Q, Lu L. Polyfluoroalkylation of 2-aminothiazoles Journal of Fluorine Chemistry. 133: 115-119. DOI: 10.1016/J.Jfluchem.2011.07.005 |
0.598 |
|
2012 |
Lin H, Dong X, Li Y, Shen Q, Lu L. Highly Selective Activation of Vinyl C–S Bonds Over Aryl C–S Bonds in the Pd‐Catalyzed Coupling of (E)‐(β‐Trifluoromethyl)vinyldiphenylsulfonium Salts: Preparation of Trifluoromethylated Alkenes and Dienes European Journal of Organic Chemistry. 2012: 4675-4679. DOI: 10.1002/Ejoc.201200758 |
0.619 |
|
2011 |
Wen L, Shen Q, Lu L. The recent development of Organofluorine chemistry in China: asymmetric construction of stereogenic trifluoromethyl-substituted carbon centers. Chimia. 65: 894-901. PMID 22273369 DOI: 10.2533/chimia.2011.894 |
0.482 |
|
2011 |
Lin H, Shen Q, Lu L. β-(Trifluoromethyl)vinyl sulfonium salts: preparation and reactions with active methylene and methenyl compounds. The Journal of Organic Chemistry. 76: 7359-69. PMID 21797270 DOI: 10.1021/Jo2009033 |
0.606 |
|
2011 |
Liu T, Shen Q. Copper-catalyzed trifluoromethylation of aryl and vinyl boronic acids with an electrophilic trifluoromethylating reagent. Organic Letters. 13: 2342-5. PMID 21473568 DOI: 10.1021/Ol2005903 |
0.781 |
|
2011 |
Wen L, Shen Q, Wan X, Lu L. Enantioselective Friedel-Crafts alkylation of indoles with trifluoroethylidene malonates by copper-bis(oxazoline) complexes: construction of trifluoromethyl-substituted stereogenic tertiary carbon center. The Journal of Organic Chemistry. 76: 2282-5. PMID 21375277 DOI: 10.1021/Jo1024333 |
0.637 |
|
2011 |
Zhang H, Shen Q, Lu L. Highly diastereoselective synthesis of optically pure trifluoromethyl-substituted imidazolidine, oxazolidine and thiazolidine Tetrahedron Letters. 52: 349-351. DOI: 10.1016/J.Tetlet.2010.11.061 |
0.625 |
|
2011 |
Qi Q, Shen Q, Lü L. Polyfluoroalkylation of 2-aminothiazoles: Unexpected sp3 c-cl substitution under mild conditions Chinese Journal of Chemistry. 29: 2681-2683. DOI: 10.1002/Cjoc.201180439 |
0.609 |
|
2010 |
Wen L, Shen Q, Lu L. Enantioselective organocatalytic Michael addition of aldehydes to trifluoroethylidene malonates. Organic Letters. 12: 4655-7. PMID 20849077 DOI: 10.1021/Ol101894H |
0.661 |
|
2010 |
Wiggins KM, Hudnall TW, Shen Q, Kryger MJ, Moore JS, Bielawski CW. Mechanical reconfiguration of stereoisomers. Journal of the American Chemical Society. 132: 3256-7. PMID 20166664 DOI: 10.1021/Ja910716S |
0.732 |
|
2009 |
Caruso MM, Davis DA, Shen Q, Odom SA, Sottos NR, White SR, Moore JS. Mechanically-induced chemical changes in polymeric materials. Chemical Reviews. 109: 5755-98. PMID 19827748 DOI: 10.1021/Cr9001353 |
0.735 |
|
2008 |
Shen Q, Hartwig JF. [(CyPF-(t)Bu)PdCl2]: an air-stable, one-component, highly efficient catalyst for amination of heteroaryl and aryl halides. Organic Letters. 10: 4109-12. PMID 18715012 DOI: 10.1021/Ol801615U |
0.553 |
|
2008 |
Shen Q, Ogata T, Hartwig JF. Highly reactive, general and long-lived catalysts for palladium-catalyzed amination of heteroaryl and aryl chlorides, bromides, and iodides: scope and structure-activity relationships. Journal of the American Chemical Society. 130: 6586-96. PMID 18444639 DOI: 10.1021/Ja077074W |
0.532 |
|
2007 |
Shen Q, Hartwig JF. Lewis acid acceleration of C-N bond-forming reductive elimination from heteroarylpalladium complexes and catalytic amidation of heteroaryl bromides. Journal of the American Chemical Society. 129: 7734-5. PMID 17542591 DOI: 10.1021/Ja0722473 |
0.555 |
|
2007 |
Hartwig JF, Shekhar S, Shen Q, Barrios-Landeros F. Synthesis of Anilines Cheminform. 38. DOI: 10.1002/9780470682531.Pat0391 |
0.801 |
|
2006 |
Fernández-Rodríguez MA, Shen Q, Hartwig JF. Highly efficient and functional-group-tolerant catalysts for the palladium-catalyzed coupling of aryl chlorides with thiols. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 7782-96. PMID 17009367 DOI: 10.1002/Chem.200600949 |
0.579 |
|
2006 |
Shen Q, Hartwig JF. Palladium-catalyzed coupling of ammonia and lithium amide with aryl halides. Journal of the American Chemical Society. 128: 10028-9. PMID 16881628 DOI: 10.1021/Ja064005T |
0.58 |
|
2006 |
Fernández-Rodríguez MA, Shen Q, Hartwig JF. A general and long-lived catalyst for the palladium-catalyzed coupling of aryl halides with thiols. Journal of the American Chemical Society. 128: 2180-1. PMID 16478149 DOI: 10.1021/Ja0580340 |
0.541 |
|
2005 |
Shen Q, Shekhar S, Stambuli JP, Hartwig JF. Highly reactive, general, and long-lived catalysts for coupling heteroaryl and aryl chlorides with primary nitrogen nucleophiles. Angewandte Chemie (International Ed. in English). 44: 1371-5. PMID 15666413 DOI: 10.1002/Anie.200462629 |
0.768 |
|
2002 |
Shen Q, Hammond GB. Regiospecific synthesis of bicyclo- and heterobicyclo-gem-difluorocyclobutenes using functionalized fluoroallenes and a novel Mo-catalyzed intramolecular [2 + 2] cycloaddition reaction. Journal of the American Chemical Society. 124: 6534-5. PMID 12047164 DOI: 10.1021/JA0263893 |
0.616 |
|
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