| Year |
Citation |
Score |
| 2024 |
Wang Z, Lin JH, Xiao JC. Photocatalytic Keto- and Amino-Trifluoromethylation of Alkenes. Organic Letters. PMID 38421197 DOI: 10.1021/acs.orglett.4c00447 |
0.608 |
|
| 2024 |
Wang JT, Wang XR, Ren JQ, Lin JH, Yu ZY, Huang SS, Hu Y, Fu JY, Wang M, Zhang YL, Wang XC, Guo JC, Xiao JC, Zhou HG. S-9-PAHSA's neuroprotective effect mediated by CAIII suppresses apoptosis and oxidative stress in a mouse model of type 2 diabetes. Cns Neuroscience & Therapeutics. 30: e14594. PMID 38332538 DOI: 10.1111/cns.14594 |
0.435 |
|
| 2023 |
Tang WY, Zheng X, Yao X, Lin JH, Zheng QT, Xiao JC. PhP/ICHCHI-promoted reductive deoxygenation of alcohols. Organic & Biomolecular Chemistry. PMID 37937947 DOI: 10.1039/d3ob01698f |
0.528 |
|
| 2023 |
Xiang YJ, Liu S, Zhou J, Lin JH, Yao X, Xiao JC. Dehydroxylative Sulfonylation of Alcohols. The Journal of Organic Chemistry. PMID 36913713 DOI: 10.1021/acs.joc.2c03085 |
0.512 |
|
| 2023 |
Chen LY, Pan PF, Lin JH, Jin CM, Xiao JC. TfO as a CF Source for the Synthesis of Trifluoromethoxylation Reagent CFSOCF. The Journal of Organic Chemistry. PMID 36763542 DOI: 10.1021/acs.joc.2c03018 |
0.562 |
|
| 2022 |
Zhang FX, Lin JH, Xiao JC. Difluoromethylsulfonyl Imidazolium Salt for Difluoromethylation of Alkenes. Organic Letters. 24: 7611-7616. PMID 36201292 DOI: 10.1021/acs.orglett.2c03073 |
0.599 |
|
| 2022 |
Zhang W, Deng X, Zhang FX, Lin JH, Xiao JC, Liang SH. Synthesis and F Labeling of Alkenyl Sulfonyl Fluorides via an Unconventional Elimination Pathway. Organic Letters. PMID 35771975 DOI: 10.1021/acs.orglett.2c02091 |
0.74 |
|
| 2022 |
Qian BY, Zhang W, Lin J, Cao W, Xiao JC. anti-Markovnikov Iodofluorination of Alkenes. Chemistry, An Asian Journal. PMID 35266316 DOI: 10.1002/asia.202200184 |
0.564 |
|
| 2021 |
Yang YF, Lin JH, Xiao JC. Starting from Styrene: A Unified Protocol for Hydrotrifluoromethylation of Diversified Alkenes. Organic Letters. PMID 34797075 DOI: 10.1021/acs.orglett.1c03630 |
0.608 |
|
| 2021 |
Zhou W, Pan WJ, Chen J, Zhang M, Lin JH, Cao W, Xiao JC. Transition-metal difluorocarbene complexes. Chemical Communications (Cambridge, England). 57: 9316-9329. PMID 34528952 DOI: 10.1039/d1cc04029d |
0.498 |
|
| 2021 |
Zhang M, Lin JH, Xiao JC. HCFSe/HCFS Installation by Tandem Substitutions from Alkyl Bromides. The Journal of Organic Chemistry. PMID 34476948 DOI: 10.1021/acs.joc.1c01718 |
0.602 |
|
| 2021 |
Zhang M, Lin JH, Xiao JC. A Readily Available Trifluoromethylation Reagent and Its Difunctionalization of Alkenes. Organic Letters. PMID 34296876 DOI: 10.1021/acs.orglett.1c02146 |
0.593 |
|
| 2021 |
Hao F, Shang X, Liu Z, Zhang H, Lin JH, Xiao JC. Rh-catalyzed tunable defluorinative borylation. Chemical Communications (Cambridge, England). PMID 34179910 DOI: 10.1039/d1cc02079j |
0.605 |
|
| 2021 |
Zhang M, Lin JH, Jin CM, Xiao JC. Difluorocarbene-based cyanodifluoromethylation of alkenes induced by a dual-functional Cu-catalyst. Chemical Communications (Cambridge, England). PMID 33587731 DOI: 10.1039/d1cc00160d |
0.54 |
|
| 2020 |
Zhang W, Gu YC, Lin JH, Xiao JC. Dehydroxylative Fluorination of Tertiary Alcohols. Organic Letters. PMID 32806144 DOI: 10.1021/Acs.Orglett.0C02438 |
0.589 |
|
| 2020 |
Lin JH, Xiao JC. Fluorinated Ylides/Carbenes and Related Intermediates from Phosphonium/Sulfonium Salts. Accounts of Chemical Research. PMID 32786338 DOI: 10.1021/Acs.Accounts.0C00244 |
0.666 |
|
| 2020 |
Xiang YQ, Yao X, Lin JH, Ou XJ, Li R, Zhou YS, Yu D, Xiao JC. The Extraction Behavior of Acidic Phosphorus-Containing Compounds to Some Metal Ions: A Combination Research of Experimental and Theoretical. The Journal of Physical Chemistry. A. PMID 32436382 DOI: 10.1021/Acs.Jpca.0C01594 |
0.506 |
|
| 2020 |
Zhang W, Lin JH, Zhang P, Xiao JC. A convenient reagent for the conversion of aldoximes into nitriles and isonitriles. Chemical Communications (Cambridge, England). PMID 32369052 DOI: 10.1039/D0Cc00188K |
0.629 |
|
| 2020 |
Zhang Y, Xiao X, Fu Z, Lin J, Guo Y, Yao X, Cao Y, Du R, Zheng X, Xiao J. Difluorocarbene-Based Cyanation of Aryl Iodides Synlett. 31: 713-717. DOI: 10.1055/S-0039-1691590 |
0.594 |
|
| 2020 |
Xiao X, Zheng Z, Li T, Zheng J, Tao T, Chen L, Gu J, Yao X, Lin J, Xiao J. Recent Advances in Difluoromethylthiolation Synthesis. 52: 197-207. DOI: 10.1055/S-0039-1690714 |
0.569 |
|
| 2020 |
He G, Jiang Y, Xiao X, Lin J, Zheng X, Du R, Cao Y, Xiao J. Difluorocarbene-based trifluoromethylthiolation of terminal alkynes Journal of Fluorine Chemistry. 230: 109437. DOI: 10.1016/J.Jfluchem.2019.109437 |
0.607 |
|
| 2020 |
Xu Z, Zhang W, Lin J, Jin C, Xiao J. Pd‐catalyzed transfer of difluorocarbene for three component cross‐coupling Chinese Journal of Chemistry. DOI: 10.1002/Cjoc.202000297 |
0.486 |
|
| 2019 |
Yu J, Lin JH, Yu D, Du R, Xiao JC. Oxidation of difluorocarbene and subsequent trifluoromethoxylation. Nature Communications. 10: 5362. PMID 31767850 DOI: 10.1038/S41467-019-13359-Z |
0.52 |
|
| 2019 |
Zhang M, Lin JH, Xiao JC. Photocatalyzed Cyanodifluoromethylation of Alkenes. Angewandte Chemie (International Ed. in English). PMID 30839151 DOI: 10.1002/Anie.201900466 |
0.595 |
|
| 2019 |
Chen XL, Zhou SH, Lin JH, Deng QH, Xiao JC. Difluorocarbene-derived trifluoromethylselenolation of benzyl halides. Chemical Communications (Cambridge, England). PMID 30640337 DOI: 10.1039/C8Cc09719D |
0.613 |
|
| 2019 |
Yu J, Lin J, Xiao J. ZnO-Promoted Wittig gem-Difluoroolefination of Aldehydes with [Ph3P+CF2H·Br-] Chinese Journal of Organic Chemistry. 39: 265. DOI: 10.6023/CJOC2018006024 |
0.506 |
|
| 2019 |
Yu J, Lin J, Cao Y, Xiao J. Visible-light-induced radical hydrodifluoromethylation of alkenes Organic Chemistry Frontiers. 6: 3580-3583. DOI: 10.1039/C9Qo00919A |
0.541 |
|
| 2019 |
Liu Z, Long J, Xiao X, Lin J, Zheng X, Xiao J, Cao Y. Ph3P+CF2CO2− as an F− and :CF2 source for trifluoromethylthiolation of alkyl halides Chinese Chemical Letters. 30: 714-716. DOI: 10.1016/J.Cclet.2018.11.013 |
0.64 |
|
| 2019 |
Zhang W, Lin J, Wu W, Cao Y, Xiao J. Dehydroxylative Trifluoromethylthiolation, Trifluoromethylation, and Difluoromethylation of Alcohols Chinese Journal of Chemistry. 38: 169-172. DOI: 10.1002/Cjoc.201900364 |
0.517 |
|
| 2018 |
Zhao Y, Lin JH, Hang XC, Xiao JC. Ag-mediated trifluoromethylthiolation of inert Csp3-H bond. The Journal of Organic Chemistry. PMID 30379072 DOI: 10.1021/Acs.Joc.8B02207 |
0.535 |
|
| 2018 |
Zhang W, Chen J, Lin JH, Xiao JC, Gu YC. Rapid Dehydroxytrifluoromethoxylation of Alcohols. Iscience. 5: 110-117. PMID 30240641 DOI: 10.1016/J.Isci.2018.07.004 |
0.592 |
|
| 2018 |
Chen J, Lin JH, Xiao JC. Dehydroxylation of alcohols for nucleophilic substitution. Chemical Communications (Cambridge, England). PMID 29873348 DOI: 10.1039/C8Cc03856B |
0.61 |
|
| 2018 |
Chen J, Lin JH, Xiao JC. Halogenation through Deoxygenation of Alcohols and Aldehydes. Organic Letters. PMID 29741387 DOI: 10.1021/Acs.Orglett.8B01058 |
0.608 |
|
| 2018 |
Lin J, Zheng X, Xiao J, Long J, Chen J, Li R, Liu Z, Xiao X. Ph3P/I–-Promoted Dichlorination or Dibromination of Epoxides with XCH2CH2X (X = Cl or Br) Synlett. 30: 181-184. DOI: 10.1055/S-0037-1610308 |
0.605 |
|
| 2018 |
Pan X, Zhao Y, Qu H, Lin J, Hang X, Xiao J. Tri- and di-fluoroethylation of alkenes by visible light photoredox catalysis Organic Chemistry Frontiers. 5: 1452-1456. DOI: 10.1039/C8Qo00082D |
0.6 |
|
| 2018 |
Chen J, Lin J, Xiao J. Decarboxylative nucleophilic difluoromethylation of aldehydes and imines Tetrahedron. 74: 4295-4297. DOI: 10.1016/J.Tet.2018.06.062 |
0.639 |
|
| 2018 |
Zhang W, Lin J, Xiao J. Cu-catalyzed chlorotrifluoromethylation of alkenes with CF3SO2Cl Journal of Fluorine Chemistry. 215: 25-31. DOI: 10.1016/J.Jfluchem.2018.09.001 |
0.61 |
|
| 2017 |
Xiao JC, Yu J, Lin J. Reaction of thiocarbonyl fluoride formed from difluorocarbene with amines. Angewandte Chemie (International Ed. in English). PMID 29143469 DOI: 10.1002/Anie.201710186 |
0.651 |
|
| 2017 |
Luo JJ, Zhang M, Lin JH, Xiao JC. Difluorocarbene for dehydroxytrifluoromethylthiolation of alcohols. The Journal of Organic Chemistry. PMID 28910103 DOI: 10.1021/Acs.Joc.7B01701 |
0.557 |
|
| 2017 |
Huang QX, Zheng QT, Duan Y, Lin JH, Xiao JC, Zheng X. Diastereoselective synthesis of CF3-containing vicinal diamines. The Journal of Organic Chemistry. PMID 28686431 DOI: 10.1021/Acs.Joc.7B01261 |
0.786 |
|
| 2017 |
Duan Y, Lin JH, Xiao JC, Gu YC. Difluoromethylcarbene for iron-catalyzed cyclopropanation. Chemical Communications (Cambridge, England). PMID 28317978 DOI: 10.1039/C7Cc01636K |
0.776 |
|
| 2017 |
Zheng J, Cheng R, Lin JH, Yu DH, Ma L, Jia L, Zhang L, Wang L, Xiao JC, Liang SH. An Unconventional Mechanistic Insight into SCF3 Formation from Difluorocarbene: Preparation of (18) F-Labeled α-SCF3 Carbonyl Compounds. Angewandte Chemie (International Ed. in English). PMID 28194833 DOI: 10.1002/Anie.201611761 |
0.577 |
|
| 2017 |
Duan Y, Lin J, Xiao J, Gu Y. Fe-Catalyzed insertion of fluoromethylcarbenes generated from sulfonium salts into X–H bonds (X = Si, C, P) Organic Chemistry Frontiers. 4: 1917-1920. DOI: 10.1039/C7Qo00430C |
0.755 |
|
| 2017 |
Zeng X, Deng Z, Liu C, Zhao G, Lin J, Zheng X, Xiao J. Nucleophilic monofluoroalkylation with fluorinated phosphonium salt toward carbonyl and imine compounds Journal of Fluorine Chemistry. 193: 17-23. DOI: 10.1016/J.Jfluchem.2016.11.012 |
0.626 |
|
| 2016 |
Deng Z, Liu C, Zeng XL, Lin JH, Xiao JC. Nucleophilic 1,1-Difluoroethylation with Fluorinated Phosphonium Salt. The Journal of Organic Chemistry. 81: 12084-12090. PMID 27978722 DOI: 10.1021/Acs.Joc.6B02723 |
0.609 |
|
| 2016 |
Deng XY, Lin JH, Xiao JC. Pd-Catalyzed Transfer of Difluorocarbene. Organic Letters. PMID 27517865 DOI: 10.1021/Acs.Orglett.6B02141 |
0.74 |
|
| 2016 |
Deng Z, Lin JH, Cai J, Xiao JC. Direct Nucleophilic Difluoromethylation of Carbonyl Compounds. Organic Letters. PMID 27281283 DOI: 10.1021/Acs.Orglett.6B01425 |
0.639 |
|
| 2016 |
Duan Y, Lin JH, Xiao JC, Gu YC. A Trifluoromethylcarbene Source. Organic Letters. PMID 27169696 DOI: 10.1021/Acs.Orglett.6B01042 |
0.776 |
|
| 2016 |
Ji YL, Luo JJ, Lin JH, Xiao JC, Gu YC. Cu-Catalyzed C-H Trifluoromethylation of 3-Arylprop-1-ynes for the Selective Construction of Allenic Csp(2)-CF3 and Propargyl Csp(3)-CF3 Bonds. Organic Letters. PMID 26883382 DOI: 10.1021/Acs.Orglett.6B00120 |
0.599 |
|
| 2016 |
Deng Z, Lin JH, Xiao JC. Nucleophilic arylation with tetraarylphosphonium salts. Nature Communications. 7: 10337. PMID 26822205 DOI: 10.1038/Ncomms10337 |
0.654 |
|
| 2016 |
Zheng Q, Wei Y, Zheng J, Duan Y, Zhao G, Wang Z, Lin J, Zheng X, Xiao J. Difluoromethylation of N-arylsulfonyl hydrazones with difluorocarbene leading to difluoromethyl aryl sulfones Rsc Advances. 6: 82298-82300. DOI: 10.1039/C6Ra20629H |
0.77 |
|
| 2016 |
Zhou S, Lin J, Zhao G, Xiao J, Cao W. Hydroperfluoroalkylation of electron-deficient olefins with perfluoroalkyl iodides promoted by zinc/viologen Rsc Advances. 6: 60080-60083. DOI: 10.1039/C6Ra11557H |
0.503 |
|
| 2016 |
Yue CB, Lin JH, Cai J, Zhang CP, Zhao G, Xiao JC, Li HF. O-Difluoromethylation of 1,3-diones with S-difluoromethyl sulfonium salt Rsc Advances. 6: 35705-35708. DOI: 10.1039/C6Ra06338A |
0.526 |
|
| 2016 |
Liu C, Deng X, Zeng X, Zhao G, Lin J, Wang H, Xiao J. Base-free O-difluoromethylation of 1,3-diones with difluorocarbene Journal of Fluorine Chemistry. 192: 27-30. DOI: 10.1016/J.Jfluchem.2016.10.011 |
0.761 |
|
| 2016 |
Wei Y, Yu L, Lin J, Zheng X, Xiao J. DBU-Promoted Trifluoromethylation of Aryl Iodides with Difluoromethyltriphenylphosphonium Bromide Chinese Journal of Chemistry. 34: 481-484. DOI: 10.1002/Cjoc.201500543 |
0.627 |
|
| 2016 |
Zheng Q, Wei Y, Zheng J, Duan Y, Zhao G, Wang Z, Lin J, Zheng X, Xiao J. ChemInform Abstract: Difluoromethylation of N-Arylsulfonyl Hydrazones with Difluorocarbene Leading to Difluoromethyl Aryl Sulfones. Cheminform. 47. DOI: 10.1002/CHIN.201652071 |
0.727 |
|
| 2016 |
Zheng J, Lin J, Yu L, Wei Y, Zheng X, Xiao J. ChemInform Abstract: Cross-Coupling Between Difluorocarbene and Carbene-Derived Intermediates Generated from Diazocompounds for the Synthesis of gem-Difluoroolefins. Cheminform. 47. DOI: 10.1002/CHIN.201618048 |
0.545 |
|
| 2016 |
Zheng J, Wang L, Lin J, Xiao J, Liang SH. ChemInform Abstract: Difluorocarbene-Derived Trifluoromethylthiolation and [18F]Trifluoromethylthiolation of Aliphatic Electrophiles. Cheminform. 47: no-no. DOI: 10.1002/CHIN.201609088 |
0.509 |
|
| 2015 |
Zheng J, Lin JH, Yu LY, Wei Y, Zheng X, Xiao JC. Cross-Coupling between Difluorocarbene and Carbene-Derived Intermediates Generated from Diazocompounds for the Synthesis of gem-Difluoroolefins. Organic Letters. PMID 26636182 DOI: 10.1021/Acs.Orglett.5B03159 |
0.585 |
|
| 2015 |
Zheng J, Wang L, Lin JH, Xiao JC, Liang SH. Difluorocarbene-Derived Trifluoromethylthiolation and [(18) F]Trifluoromethylthiolation of Aliphatic Electrophiles. Angewandte Chemie (International Ed. in English). PMID 26387796 DOI: 10.1002/Anie.201505446 |
0.615 |
|
| 2015 |
Duan Y, Zhou B, Lin JH, Xiao JC. Diastereoselective Johnson-Corey-Chaykovsky trifluoroethylidenation. Chemical Communications (Cambridge, England). PMID 26189644 DOI: 10.1039/C5Cc04991A |
0.797 |
|
| 2015 |
Deng XY, Lin JH, Zheng J, Xiao JC. Difluoromethylation and gem-difluorocyclopropenation with difluorocarbene generated by decarboxylation. Chemical Communications (Cambridge, England). 51: 8805-8. PMID 25918009 DOI: 10.1039/C5Cc02736E |
0.739 |
|
| 2015 |
Zheng J, Lin JH, Deng XY, Xiao JC. 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU)-promoted decomposition of difluorocarbene and the subsequent trifluoromethylation. Organic Letters. 17: 532-5. PMID 25587871 DOI: 10.1021/Ol503548S |
0.736 |
|
| 2015 |
Deng X, Lin J, Xiao J. One-pot synthesis of gem-difluorostyrenes from benzyl bromide via olefination of phosphonium ylide with difluorocarbene Journal of Fluorine Chemistry. 179: 116-120. DOI: 10.1016/J.Jfluchem.2015.06.009 |
0.786 |
|
| 2015 |
Deng X, Lin J, Zheng J, Xiao J. ChemInform Abstract: Difluoromethylation and gem-Difluorocyclopropenation with Difluorocarbene Generated by Decarboxylation. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201538060 |
0.506 |
|
| 2015 |
Ji Y, Lin J, Xiao J, Gu Y. ChemInform Abstract: Stereoselective Synthesis of α-Trifluoromethyl Enones by AuI/CuI-Co-Catalyzed Tandem 1,3-Acyloxy Migration/Trifluoromethylation Reaction of Propargyl Acetates. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201517081 |
0.33 |
|
| 2015 |
Deng X, Lin J, Zheng J, Xiao J. ChemInform Abstract: Cu-Promoted Oxidative Trifluoromethylation of Terminal Alkynes with Difluoromethylene Phosphobetaine. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201508093 |
0.496 |
|
| 2014 |
Ji YL, Kong JJ, Lin JH, Xiao JC, Gu YC. Copper-mediated trifluoromethylation of propargyl acetates leading to trifluoromethyl-allenes Organic and Biomolecular Chemistry. 12: 2903-2906. PMID 24676349 DOI: 10.1039/C3Ob42575D |
0.608 |
|
| 2014 |
Yang TP, Li Q, Lin JH, Xiao JC. Boron-trihalide-promoted regioselective ring-opening reactions of gem-difluorocyclopropyl ketones. Chemical Communications (Cambridge, England). 50: 1077-9. PMID 24310244 DOI: 10.1039/C3Cc47879C |
0.626 |
|
| 2014 |
Zhang H, Lin JH, Xiao JC, Gu YC. Rh-catalyzed allylic C-F bond activation: the stereoselective synthesis of trisubstituted monofluoroalkenes and a mechanism study. Organic & Biomolecular Chemistry. 12: 581-8. PMID 24287644 DOI: 10.1039/C3Ob42038H |
0.607 |
|
| 2014 |
Ji Y, Lin J, Xiao J, Gu Y. Copper-catalyzed tandem trifluoromethylation/cyclization of internal alkynes Organic Chemistry Frontiers. 1: 1280-1284. DOI: 10.1039/C4Qo00240G |
0.647 |
|
| 2014 |
Lin J, Xiao J. Recent advances in asymmetric fluorination and fluoroalkylation reactions via organocatalysis Tetrahedron Letters. 55: 6147-6155. DOI: 10.1016/J.Tetlet.2014.09.031 |
0.581 |
|
| 2014 |
Li Q, Lin J, Deng Z, Zheng J, Cai J, Xiao J. Wittig gem-difluoroolefination of aldehydes with difluoromethyltriphenylphosphonium bromide Journal of Fluorine Chemistry. 163: 38-41. DOI: 10.1016/J.Jfluchem.2014.04.011 |
0.56 |
|
| 2014 |
Gu W, Lin J, Xiao J. Direct N-gem-difluorocyclopropylation of nitro-heterocycles by utilizing gem-difluorocyclopropyl tosylate Chinese Chemical Letters. 25: 24-28. DOI: 10.1016/J.Cclet.2013.11.027 |
0.527 |
|
| 2014 |
Ji Y, Lin J, Xiao J, Gu Y. Stereoselective Synthesis of α‐Trifluoromethyl Enones by AuI/CuI‐Co‐Catalyzed Tandem 1,3‐Acyloxy Migration/Trifluoromethylation Reaction of Propargyl Acetates European Journal of Organic Chemistry. 2014: 7948-7954. DOI: 10.1002/Ejoc.201403115 |
0.626 |
|
| 2014 |
Wang X, Lin J, Xiao J, Zheng X. Decarboxylative Julia–Kocienski gem‐Difluoro‐Olefination of 2‐Pyridinyl Sulfonyldifluoroacetate European Journal of Organic Chemistry. 2014: 928-932. DOI: 10.1002/Ejoc.201301654 |
0.599 |
|
| 2014 |
Deng X, Lin J, Zheng J, Xiao J. Cu-Promoted Oxidative Trifluoromethylation of Terminal Alkynes with Difluoromethylene Phosphobetaine Chinese Journal of Chemistry. 32: 689-693. DOI: 10.1002/Cjoc.201400427 |
0.736 |
|
| 2014 |
Li Q, Lin J, Deng Z, Zheng J, Cai J, Xiao J. ChemInform Abstract: Wittig gem-Difluoroolefination of Aldehydes with Difluoromethyltriphenylphosphonium Bromide. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201446048 |
0.579 |
|
| 2014 |
Zheng J, Lin J, Cai J, Xiao J. ChemInform Abstract: Conversion Between Difluorocarbene and Difluoromethylene Ylide. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201414069 |
0.528 |
|
| 2013 |
Wang XP, Lin JH, Zhang CP, Xiao JC, Zheng X. Copper-catalyzed trifluoromethylation of alkenes with an electrophilic trifluoromethylating reagent. Beilstein Journal of Organic Chemistry. 9: 2635-40. PMID 24367428 DOI: 10.3762/Bjoc.9.299 |
0.795 |
|
| 2013 |
Zheng J, Lin JH, Cai J, Xiao JC. Conversion between difluorocarbene and difluoromethylene ylide. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 15261-6. PMID 24114936 DOI: 10.1002/Chem.201303248 |
0.654 |
|
| 2013 |
Yang TP, Lin JH, Chen QY, Xiao JC. A novel reaction of gem-difluorocyclopropyl ketones with nitriles leading to 2-fluoropyrroles. Chemical Communications (Cambridge, England). 49: 9833-5. PMID 24030730 DOI: 10.1039/C3Cc45456H |
0.719 |
|
| 2013 |
Zheng J, Cai J, Lin JH, Guo Y, Xiao JC. Synthesis and decarboxylative Wittig reaction of difluoromethylene phosphobetaine. Chemical Communications (Cambridge, England). 49: 7513-5. PMID 23863949 DOI: 10.1039/C3Cc44271C |
0.648 |
|
| 2013 |
Wang X, Lin J, Zhang C, Xiao J, Zheng X. Copper-Mediated Trifluoromethylation of Terminal Alkynes by S-(Trifluoromethyl) diarylsulfonium Salt Chinese Journal of Chemistry. 31: 915-920. DOI: 10.1002/Cjoc.201300393 |
0.595 |
|
| 2013 |
Zheng J, Cai J, Lin J, Guo Y, Xiao J. ChemInform Abstract: Synthesis and Decarboxylative Wittig Reaction of Difluoromethylene Phosphobetaine. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201350041 |
0.61 |
|
| 2012 |
Lin JH, Zong G, Du RB, Xiao JC, Liu S. The asymmetric synthesis of CF3- or -CF2-substituted tetrahydroquinolines by employing a chiral phosphoric acid as catalyst. Chemical Communications (Cambridge, England). 48: 7738-40. PMID 22779079 DOI: 10.1039/C2Cc18064B |
0.623 |
|
| 2010 |
Zhu Z, Jiang M, Lin J, Zhang C, Hang X, Zheng C, Chen Q, Xiao J. ChemInform Abstract: Unexpected Reactions of PushâPull N-Heterocyclic Carbene Derived from N-(4-Methoxyphenyl)-N-(4-nitrophenyl)-imidazolium Chloride. Cheminform. 41. DOI: 10.1002/CHIN.201003121 |
0.542 |
|
| 2009 |
Zhu ZQ, Jiang MY, Lin JH, Zhang CP, Hang XC, Zheng CG, Chen QY, Xiao JC. Unexpected reactions of push-pull N-heterocyclic carbene derived from N-(4-methoxyphenyl)-N-(4-nitrophenyl)-imidazolium chloride Synlett. 2305-2308. DOI: 10.1055/S-0029-1217813 |
0.71 |
|
| 2009 |
Lin J, Zhang C, Xiao J. Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water Green Chemistry. 11: 1750. DOI: 10.1039/B916583E |
0.61 |
|
| 2009 |
Lin J, Zhang C, Zhu Z, Chen Q, Xiao J. Corrigendum to “A novel pyrrolidinium ionic liquid with 1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoroethoxy)ethanesulfonate anion as a recyclable reaction medium and efficient catalyst for Friedel–Crafts alkylations of indoles with nitroalkenes” [J. Fluorine Chem. 130 (2009) 394–398] Journal of Fluorine Chemistry. 130: 604. DOI: 10.1016/J.Jfluchem.2009.04.005 |
0.669 |
|
| 2009 |
Lin J, Zhang C, Zhu Z, Chen Q, Xiao J. A novel pyrrolidinium ionic liquid with 1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoroethoxy)ethanesulfonate anion as a recyclable reaction medium and efficient catalyst for Friedel–Crafts alkylations of indoles with nitroalkenes Journal of Fluorine Chemistry. 130: 394-398. DOI: 10.1016/J.Jfluchem.2009.01.004 |
0.681 |
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| 2009 |
Lin J, Zhang C, Zhu Z, Chen Q, Xiao J. ChemInform Abstract: A Novel Pyrrolidinium Ionic Liquid with 1,1,2,2-Tetrafluoro-2-(1,1,2,2-tetrafluoroethoxy)ethanesulfonate Anion as a Recyclable Reaction Medium and Efficient Catalyst for Friedel-Crafts Alkylations of Indoles with Nitroalkenes. Cheminform. 40. DOI: 10.1002/CHIN.200935118 |
0.575 |
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