Year |
Citation |
Score |
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 |
0.536 |
|
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 |
0.514 |
|
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 |
0.562 |
|
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 |
0.554 |
|
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 |
0.54 |
|
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 |
0.571 |
|
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 |
0.595 |
|
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 |
0.641 |
|
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 |
0.612 |
|
2018 |
Zhang H, Shen W, Lu L. Cycloadditions between methyl (Z)-2-bromo-4,4,4-trifluoro-2-butenoate and various tosylacetamides: Synthesis of trifluoromethylated pyroglutamates and 2-pyridones derivatives Tetrahedron Letters. 59: 1042-1045. DOI: 10.1016/J.Tetlet.2018.01.095 |
0.404 |
|
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 |
0.529 |
|
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 |
0.617 |
|
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 |
0.615 |
|
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 |
0.582 |
|
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 |
0.759 |
|
2017 |
Liu X, Ma H, Xing C, Lu L. Alkynylation of cyclopropyl trifluoromethyl ketone catalyzed by CuF2·2H2O/4,7-diphenyl-1,10-phenanthroline Tetrahedron Letters. 58: 1564-1567. DOI: 10.1016/J.Tetlet.2017.03.010 |
0.389 |
|
2017 |
Liu X, Wang Y, Ma H, Xing C, Yuan Y, Lu L. Cs2CO3-catalyzed alkylation of indoles with trifluoromethyl ketones Tetrahedron. 73: 2283-2289. DOI: 10.1016/J.Tet.2017.03.012 |
0.485 |
|
2017 |
Liu X, Ma H, Xing C, Lu L. Synthesis of trifluoromethyl-/cyclopropyl-substituted 2-isoxazolines by DBU-promoted domino reaction Chinese Chemical Letters. 28: 1780-1783. DOI: 10.1016/J.Cclet.2017.03.031 |
0.489 |
|
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 |
0.776 |
|
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 |
0.612 |
|
2016 |
Li C, Cai LZ, Liu XD, Zhu SZ, Xing CH, Lu L. Highly efficient synthesis of tetrasubstituted 2,3-dihydropyrans by three-component 'one-pot' reaction Tetrahedron Letters. 57: 2171-2174. DOI: 10.1016/J.Tetlet.2016.04.008 |
0.432 |
|
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 |
0.783 |
|
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 |
0.659 |
|
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 |
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 |
0.644 |
|
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 |
0.591 |
|
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 |
0.622 |
|
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 |
0.762 |
|
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 |
0.777 |
|
2014 |
Wang Y, Yuan Y, Xing C, Lu L. Trifluoromethanesulfonic acid-catalyzed solvent-free bisindolylation of trifluoromethyl ketones Tetrahedron Letters. 55: 1045-1048. DOI: 10.1016/J.Tetlet.2013.12.078 |
0.488 |
|
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 |
0.66 |
|
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 |
0.548 |
|
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 |
0.605 |
|
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 |
0.629 |
|
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 |
0.586 |
|
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 |
0.6 |
|
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 |
0.615 |
|
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 |
0.658 |
|
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 |
0.713 |
|
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 |
0.578 |
|
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 |
0.566 |
|
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 |
0.638 |
|
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 |
0.627 |
|
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 |
0.593 |
|
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 |
0.612 |
|
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 |
0.472 |
|
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 |
0.604 |
|
2011 |
Wang H, Xu C, Zhang L, Tang Q, Guo Y, Lu L. Investigation of coordination of Mg(II) cations to 2-pyrimidinyloxy-N-arylbenzylamines by electrospray mass spectrometry: insights for Mg(II) catalyzed Smiles rearrangement reactions. European Journal of Mass Spectrometry (Chichester, England). 17: 145-57. PMID 21719923 DOI: 10.1255/Ejms.1122 |
0.312 |
|
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 |
0.626 |
|
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 |
0.628 |
|
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 |
0.607 |
|
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 |
0.655 |
|
2010 |
Yang Z, Lu L. Synthesis of deuterated herbicidal ZJ0273, ZJ0702, ZJ0777, and SIOC0163 Journal of Labelled Compounds and Radiopharmaceuticals. 53: 192-197. DOI: 10.1002/Jlcr.1749 |
0.336 |
|
2010 |
Huang W, Lü L. The reaction of perfluoroalkanesulfinates VII. Fenton reagent-initiated addition of sodium perfluoroalkanesulfinates to alkenes Chinese Journal of Chemistry. 10: 365-372. DOI: 10.1002/Cjoc.19920100413 |
0.412 |
|
2010 |
Huang W, Lü L. The reaction of perfluoroalkanesulfonyl halides VII. Preparation and reactions of trifluoromethanesulfonyl bromide Chinese Journal of Chemistry. 10: 268-273. DOI: 10.1002/Cjoc.19920100312 |
0.445 |
|
2010 |
Huang W, Lü L. Synthesis of perfluoroalkyl-containing steroidal glycosides† Chinese Journal of Chemistry. 10: 262-267. DOI: 10.1002/Cjoc.19920100311 |
0.372 |
|
2009 |
Liu T, Zhao X, Lu L, Cohen T. Readily prepared 3-chloro-1-(phenylthio)propene, a versatile three-carbon annulating agent. Organic Letters. 11: 4576-9. PMID 19772307 DOI: 10.1021/Ol901818J |
0.312 |
|
2008 |
Yang Z, Ye Q, Lu L. Synthesis of herbicidal ZJ0273 labeled with tritium and carbon‐14 Journal of Labelled Compounds and Radiopharmaceuticals. 51: 182-186. DOI: 10.1002/Jlcr.1498 |
0.341 |
|
2007 |
Wang HY, Zhang X, Guo YL, Lu L. Mass spectrometric studies of the gas phase retro-Michael type fragmentation reactions of 2-hydroxybenzyl-N-pyrimidinylamine derivatives. Journal of the American Society For Mass Spectrometry. 16: 1561-1573. PMID 16006143 DOI: 10.1016/J.Jasms.2005.05.006 |
0.316 |
|
2007 |
Zhang J, Zhao X, Lu L. Novel synthesis of 3-(3,3,3-trifluoroprop-1-en-2-yl)furans via stereoselective processing and palladium-catalyzed cycloisomerization Tetrahedron Letters. 48: 1911-1913. DOI: 10.1016/J.Tetlet.2007.01.097 |
0.405 |
|
2006 |
Chen W, Zhao X, Lu L, Cohen T. 2-Phenylthio-3-bromopropene, a valuable synthon, easily prepared by a simple rearrangement. Organic Letters. 8: 2087-90. PMID 16671788 DOI: 10.1021/Ol0605171 |
0.423 |
|
2006 |
Wang H, Zhao X, Li Y, Lu L. Solvent-controlled asymmetric Strecker reaction: stereoselective synthesis of alpha-trifluoromethylated alpha-amino acids. Organic Letters. 8: 1379-81. PMID 16562896 DOI: 10.1021/Ol0601186 |
0.322 |
|
2006 |
Wang HY, Zhang X, Guo YL, Tang QH, Lu L. Using Tandem Mass Spectrometry to Predict Chemical Transformations of 2-Pyrimidinyloxy-N-Arylbenzyl Amine Derivatives in Solution Journal of the American Society For Mass Spectrometry. 17: 253-263. PMID 16413200 DOI: 10.1016/J.Jasms.2005.11.001 |
0.424 |
|
2006 |
Zhang J, Zhao X, Li Y, Lu L. Highly efficient synthesis of 4-trifluoromethylfuran derivatives via a sequential deprotection-annulation reaction Tetrahedron Letters. 47: 4737-4739. DOI: 10.1016/J.Tetlet.2006.04.110 |
0.424 |
|
2005 |
Wang H, Liao Y, Guo Y, Tang Q, Lu L. Interesting Acid-Catalyzed O-N-Type Smiles Rearrangement Reactions of 2-Pyrimidinyloxy-N-Arylbenzylamine Derivatives Synlett. 2005: 1239-1242. DOI: 10.1055/S-2005-865235 |
0.448 |
|
2005 |
Wang H, Zhang X, Guo Y, Dong X, Tang Q, Lu L. Sulfonamide bond cleavage in benzenesulfonamides and rearrangement of the resulting p‐aminophenylsulfonyl cations: application to a 2‐pyrimidinyloxybenzylaminobenzenesulfonamide herbicide Rapid Communications in Mass Spectrometry. 19: 1696-1702. DOI: 10.1002/Rcm.1978 |
0.302 |
|
2004 |
Wang H, Guo Y, Lu L. Studies of rearrangement reactions of protonated and lithium cationized 2-pyrimidinyloxy-N-arylbenzylamine derivatives by MALDI-FT-ICR mass spectrometry. Journal of the American Society For Mass Spectrometry. 15: 1820-1832. PMID 15589758 DOI: 10.1016/J.Jasms.2004.08.014 |
0.356 |
|
2004 |
Li Y, Lu L, Zhao X. High stereoselective preparation of O-protected 2-trifluoromethyl 3-bromoallylic alcohols from 1,1-dibromo-1-alkenes. Organic Letters. 6: 4467-70. PMID 15548052 DOI: 10.1021/Ol0482341 |
0.322 |
|
2004 |
Wang Y, Zhao X, Li Y, Lu L. Stereospecific synthesis of trifluoromethyl-substituted polyfunctionalized cyclopropanes Tetrahedron Letters. 45: 7775-7777. DOI: 10.1016/J.Tetlet.2004.08.064 |
0.424 |
|
2004 |
Li Y, Zhao X, Lu L. A facile approach to fluorinated tetra-substituted alkenes via bis-Suzuki coupling reaction of 2-trifluoromethyl-1,1-dibromoalkenes Journal of Fluorine Chemistry. 125: 1821-1824. DOI: 10.1016/J.Jfluchem.2004.06.004 |
0.491 |
|
2001 |
Wang H, Ling W, Lu L. A novel resin-bound CF3-containing building block: application to the solid-phase synthesis of CF3-containing acrylates and 4-isoxazolecarboxylates Journal of Fluorine Chemistry. 111: 241-246. DOI: 10.1016/S0022-1139(01)00461-4 |
0.41 |
|
2000 |
Zhang Q, Lu L. A novel synthetic route to ethyl 3-substituted-trans-2,3-difluoro-2-acrylates and their reactions with nucleophiles Tetrahedron Letters. 41: 8545-8548. DOI: 10.1016/S0040-4039(00)01517-3 |
0.496 |
|
1996 |
Wu F, Huang B, Lu L, Huang W. Addition reactions of dibromodifluoromethane promoted by sulfinatodehalogenation reagents Journal of Fluorine Chemistry. 80: 91-94. DOI: 10.1016/S0022-1139(96)03503-8 |
0.428 |
|
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