| Year |
Citation |
Score |
| 2019 |
Dong J, Guo H, Peng W, Hu Q. Room temperature Pd(0)/Ad3P-catalyzed coupling reactions of aryl chlorides with bis(pinacolato)diboron Tetrahedron Letters. 60: 760-763. DOI: 10.1016/J.Tetlet.2019.01.042 |
0.549 |
|
| 2019 |
Peng W, Dong J, Li H, Chow C, Hu Q. Room temperature suzuki cross‐coupling polymerizations of aryl dihalides and aryldiboronic acid/acid esters with
t
‐Bu
3
P‐coordinated 2‐phenylaniline‐based palladacycle complex as the precatalyst Journal of Polymer Science Part a: Polymer Chemistry. 57: 1606-1611. DOI: 10.1002/Pola.29427 |
0.431 |
|
| 2018 |
Liao YX, Dong J, Hu QS. Ir(COD)Cl]/Tris(2,4-di--butylphenyl)phosphite-Catalyzed Addition Reactions of Arylboronic Acids with Aldehydes. Tetrahedron Letters. 59: 1548-1550. PMID 30333670 DOI: 10.1016/J.Tetlet.2018.02.071 |
0.72 |
|
| 2017 |
Dong J, Guo H, Hu Q. Controlled Pd(0)/Ad3P-Catalyzed Suzuki Cross-Coupling Polymerization of AB-Type Monomers with Ad3P-Coordinated Acetanilide-Based Palladacycle Complex as Initiator Acs Macro Letters. 6: 1301-1304. DOI: 10.1021/Acsmacrolett.7B00759 |
0.363 |
|
| 2017 |
Dong J, Guo H, Hu Q. Room Temperature Ni0
/PCy3
-Catalyzed Coupling Reactions of Aryl Arenesulfonates with Bis(pinacolato)diboron European Journal of Organic Chemistry. 2017: 7087-7090. DOI: 10.1002/Ejoc.201701300 |
0.491 |
|
| 2016 |
Chen WB, Xing CH, Dong J, Hu QS. Electron-Poor, Fluoro-Containing Arylboronic Acids as Efficient Coupling Partners for Bis(1,5-cyclooctadiene)nickel(0)/Tricyclohexylphosphine-Catalyzed Cross-Coupling Reactions of Aryl Arenesulfonates. Advanced Synthesis & Catalysis. 358: 2072-2076. PMID 28751852 DOI: 10.1002/Adsc.201600205 |
0.503 |
|
| 2016 |
Zhang H, Peng W, Dong J, Hu Q. t-Bu3P-Coordinated 2-Phenylaniline-Based Palladacycle Complex/ArBr as Robust Initiators for Controlled Pd(0)/t-Bu3P-Catalyzed Suzuki Cross-Coupling Polymerization of AB-Type Monomers Acs Macro Letters. 5: 656-660. DOI: 10.1021/Acsmacrolett.6B00230 |
0.333 |
|
| 2016 |
Chen W, Xing C, Dong J, Hu Q. ChemInform Abstract: Electron-Poor, Fluoro-Containing Arylboronic Acids as Efficient Coupling Partners for Bis(1,5-cyclooctadiene)nickel(0)/Tricyclohexylphosphine-Catalyzed Cross-Coupling Reactions of Aryl Arenesulfonates. Cheminform. 47. DOI: 10.1002/CHIN.201648095 |
0.427 |
|
| 2015 |
Liu R, Liu Z, Xu Y, Liao Y, Hu Q, Huang J, Shi X, Li Y, Niu J, Li Q. Multicolor Melting Curve Analysis-Based Multilocus Melt Typing of Vibrio parahaemolyticus. Plos One. 10: e0136998. PMID 26368129 DOI: 10.1371/Journal.Pone.0136998 |
0.449 |
|
| 2015 |
Zhang HH, Hu QS, Hong K. Accessing conjugated polymers with precisely controlled heterobisfunctional chain ends via post-polymerization modification of the OTf group and controlled Pd(0)/t-Bu3P-catalyzed Suzuki cross-coupling polymerization. Chemical Communications (Cambridge, England). 51: 14869-72. PMID 26299669 DOI: 10.1039/C5Cc06188A |
0.306 |
|
| 2015 |
Liao Y, Li Y, Wu S, Mou J, Xu Z, Cui R, Klena JD, Shi X, Lu Y, Qiu Y, Lin Y, Xie X, Ma H, Li Z, Yu H, ... ... Hu Q, et al. Risk Factors for Vibrio parahaemolyticus Infection in a Southern Coastal Region of China. Foodborne Pathogens and Disease. PMID 26287765 DOI: 10.1089/Fpd.2015.1988 |
0.419 |
|
| 2014 |
Zhang HH, Dong J, Hu QS. tBu3P-Coordinated 2-Phenylaniline-Based Palladacycle Complex As Precatalyst for Pd-Catalyzed Coupling Reactions of Aryl Halides with Polyfluoroarenes via C-H Activation Strategy. European Journal of Organic Chemistry. 2014: 1327-1332. PMID 24778575 DOI: 10.1002/Ejoc.201301272 |
0.491 |
|
| 2014 |
Zhang H, Dong J, Hu Q. ChemInform Abstract: tBu3P-Coordinated 2-Phenylaniline-Based Palladacycle Complexes as Precatalyst for Pd-Catalyzed Coupling Reactions of Aryl Halides with Polyfluoroarenes by a C-H Activation Strategy. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201449048 |
0.335 |
|
| 2013 |
Zhang HH, Xing CH, Tsemo GB, Hu QS. t-Bu3P-Coordinated 2-Phenylaniline-Based Palladacycle Complex as a Precatalyst for the Suzuki Cross-coupling Polymerization of Aryl Dibromides with Aryldiboronic Acids. Acs Macro Letters. 2: 10-13. PMID 23687619 DOI: 10.1021/Mz300479B |
0.442 |
|
| 2012 |
Liao YX, Hu QS. Tandem Aldol Condensation - Platinacycle-Catalyzed Addition Reactions of Aldehydes, Methyl Ketones and Arylboronic Acids. European Journal of Organic Chemistry. 2012: 5897-5901. PMID 23335856 DOI: 10.1002/Ejoc.201200867 |
0.707 |
|
| 2012 |
Liao YX, Xing CH, Hu QS. Rhodium(I)/diene-catalyzed addition reactions of arylborons with ketones. Organic Letters. 14: 1544-7. PMID 22376059 DOI: 10.1021/Ol300275S |
0.676 |
|
| 2012 |
Hu Q, Dong C. Ni(cod)2/PCy3-Catalyzed Cross-Coupling Reactions of Dihaloarenes with Arylboronic Acids Synlett. 23: 2121-2125. DOI: 10.1055/S-0031-1290455 |
0.55 |
|
| 2012 |
Liao Y, Hu Q. Tandem Aldol Condensation/Platinacycle‐Catalyzed Addition Reactions of Aldehydes, Methyl Ketones, and Arylboronic Acids (Eur. J. Org. Chem. 30/2012) European Journal of Organic Chemistry. 2012. DOI: 10.1002/Ejoc.201290081 |
0.69 |
|
| 2012 |
Xing C, Liao Y, Zhang Y, Sabarova D, Bassous M, Hu Q. Asymmetric Allylboration of Aldehydes with Pinacol Allylboronates Catalyzed by 1,1′-Spirobiindane-7,7′-diol (SPINOL) Based Phosphoric Acids European Journal of Organic Chemistry. 2012: 1115-1118. DOI: 10.1002/Ejoc.201101739 |
0.709 |
|
| 2012 |
Dong C, Hu Q. ChemInform Abstract: Ni(cod)2/PCy3-Catalyzed Cross-Coupling Reactions of Dihaloarenes with Arylboronic Acids. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201251090 |
0.461 |
|
| 2012 |
Xing C, Liao Y, Zhang Y, Sabarova D, Bassous M, Hu Q. ChemInform Abstract: Asymmetric Allylboration of Aldehydes with Pinacol Allylboronates Catalyzed by 1,1′-Spirobiindane-7,7′-diol (SPINOL) Based Phosphoric Acids. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201228065 |
0.621 |
|
| 2011 |
Liao YX, Hu QS. CuCl/bipyridine-catalyzed addition reactions of arylboroxines with aldehydes, α,β-unsaturated ketones, and N-tosyl aldimines. The Journal of Organic Chemistry. 76: 7602-7. PMID 21827191 DOI: 10.1021/Jo201338V |
0.64 |
|
| 2011 |
Qu HE, Xiao C, Wang N, Yu KH, Hu QS, Liu LX. RuCl₃·3H₂O catalyzed reactions: facile synthesis of bis(indolyl)methanes under mild conditions. Molecules (Basel, Switzerland). 16: 3855-68. PMID 21555975 DOI: 10.3390/molecules16053855 |
0.452 |
|
| 2011 |
Liu TP, Liao YX, Xing CH, Hu QS. Fluorenone synthesis by palladacycle-catalyzed sequential reactions of 2-bromobenzaldehydes with arylboronic acids. Organic Letters. 13: 2452-5. PMID 21480660 DOI: 10.1021/Ol200693D |
0.713 |
|
| 2011 |
Xing CH, Liao YX, Ng J, Hu QS. Optically active 1,1'-spirobiindane-7,7'-diol (SPINOL)-based phosphoric acids as highly enantioselective catalysts for asymmetric organocatalysis. The Journal of Organic Chemistry. 76: 4125-31. PMID 21463003 DOI: 10.1021/Jo200302X |
0.665 |
|
| 2011 |
Liao YX, Xing CH, Israel M, Hu QS. Sequential aldol condensation-transition metal-catalyzed addition reactions of aldehydes, methyl ketones, and arylboronic acids. Organic Letters. 13: 2058-61. PMID 21417359 DOI: 10.1021/Ol200457Q |
0.702 |
|
| 2011 |
Liao YX, Xing CH, Israel M, Hu QS. A nontransmetalation reaction pathway for anionic four-electron donor-based palladacycle-catalyzed addition reactions of arylborons with aldehydes Tetrahedron Letters. 52: 3324-3328. DOI: 10.1016/J.Tetlet.2011.04.074 |
0.698 |
|
| 2011 |
Xing C, Lee J, Tang Z, Zheng JR, Hu Q. ChemInform Abstract: Room Temperature Nickel(II) Complexes [(4-MeOC6H4)Ni-(PCy3)2OTs and Ni(PCy3)2X2]-Catalyzed Cross-Coupling Reactions of Aryl/Alkenyl Sulfonates with Arylboronic Acids. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201202045 |
0.37 |
|
| 2011 |
Liao Y, Xing C, Israel M, Hu Q. ChemInform Abstract: A Nontransmetalation Reaction Pathway for Anionic Four-Electron Donor-Based Palladacycle-Catalyzed Addition Reactions of Arylborons with Aldehydes. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201142058 |
0.648 |
|
| 2011 |
Xing C, Lee J, Tang Z, Zheng JR, Hu Q. Room Temperature Nickel(II) Complexes [(4-MeOC6H4)Ni(PCy3)2OTs and Ni(PCy3)2X2]-Catalyzed Cross-Coupling Reactions of Aryl/Alkenyl Sulfonates with Arylboronic Acids Advanced Synthesis & Catalysis. 353: 2051-2059. DOI: 10.1002/Adsc.201100151 |
0.52 |
|
| 2010 |
Liao YX, Hu QS. Aryl ketone synthesis via tandem orthoplatinated triarylphosphite-catalyzed addition reactions of arylboronic acids with aldehydes followed by oxidation. The Journal of Organic Chemistry. 75: 6986-9. PMID 20849092 DOI: 10.1021/Jo101469S |
0.709 |
|
| 2010 |
Xing CH, Liao YX, He P, Hu QS. Transition metal-catalyzed addition reactions of arylboronic acids with alkyl 2-formylbenzoates: efficient access to chiral 3-substituted phthalides. Chemical Communications (Cambridge, England). 46: 3010-2. PMID 20386851 DOI: 10.1039/C001104E |
0.69 |
|
| 2010 |
Liu TP, Xing CH, Hu QS. Synthesis of fluorene and indenofluorene compounds: tandem palladium-catalyzed suzuki cross-coupling and cyclization. Angewandte Chemie (International Ed. in English). 49: 2909-12. PMID 20306508 DOI: 10.1002/Anie.201000327 |
0.47 |
|
| 2010 |
Xing C, Hu Q. Ni(COD)2/4-ClC6H4COR-catalyzed addition reactions of arylboroxines with aldehydes Tetrahedron Letters. 51: 924-927. DOI: 10.1016/J.Tetlet.2009.12.033 |
0.416 |
|
| 2010 |
Liu T, Xing C, Hu Q. ChemInform Abstract: Synthesis of Fluorene and Indenofluorene Compounds: Tandem Palladium-Catalyzed Suzuki Cross-Coupling and Cyclization. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201032105 |
0.309 |
|
| 2010 |
Xing C, Hu Q. ChemInform Abstract: Ni(COD)2/4-ClC6H4COR-Catalyzed Addition Reactions of Arylboroxines with Aldehydes. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201021072 |
0.46 |
|
| 2010 |
Simonsen KB, Joergensen KA, Hu Q, Pu L. ChemInform Abstract: The First Highly Diastereo- and Enantioselective Polymeric Catalyst for the 1,3-Cycloaddition Reaction of Nitrones with Alkenes. Cheminform. 30: no-no. DOI: 10.1002/chin.199934153 |
0.447 |
|
| 2010 |
Johannsen M, Joergensen KA, Zheng X, Hu Q, Pu L. ChemInform Abstract: A Highly Enantioselective Hetero-Diels-Alder Reaction Catalyzed by Chiral Polybinaphthyl-Aluminum Complexes. Cheminform. 30: no-no. DOI: 10.1002/chin.199925029 |
0.446 |
|
| 2010 |
HUANG W, HU Q, PU L. ChemInform Abstract: A Highly General Catalyst for the Enantioselective Reaction of Aldehydes with Diethylzinc. Cheminform. 29: no-no. DOI: 10.1002/chin.199830038 |
0.44 |
|
| 2010 |
HU Q, HU C. ChemInform Abstract: Reformatsky Reactions of Ethyl 4,4-Difluoro-3-ethoxy-4-halocrotonates: Synthesis of 4,4-Difluorocarbonate Derivatives and 2-Lactenones. Cheminform. 28: no-no. DOI: 10.1002/chin.199744153 |
0.461 |
|
| 2009 |
Hu Q, Dong C, Liu T. Monoarylation of Dibromoarenes by Simple Palladium Catalyst Systems: Efficient Synthesis of Bromobiaryls from Dibromoarenes and Arylboronic Acids Synlett. 2009: 1081-1086. DOI: 10.1055/S-0028-1088110 |
0.358 |
|
| 2009 |
Xing C, Liu T, Zheng JR, Ng J, Esposito M, Hu Q. Rh(I)/diene-catalyzed addition reactions of aryl/alkenylboronic acids with aldehydes Tetrahedron Letters. 50: 4953-4957. DOI: 10.1016/J.Tetlet.2009.06.074 |
0.618 |
|
| 2009 |
Xing C, Liu T, Zheng JR, Ng J, Esposito M, Hu Q. ChemInform Abstract: Rh(I)/Diene-Catalyzed Addition Reactions of Aryl/Alkenylboronic Acids with Aldehydes. Cheminform. 40. DOI: 10.1002/chin.200949089 |
0.548 |
|
| 2009 |
Dong C, Liu T, Hu Q. ChemInform Abstract: Monoarylation of Dibromoarenes by Simple Palladium Catalyst Systems: Efficient Synthesis of Bromobiaryls from Dibromoarenes and Arylboronic Acids. Cheminform. 40. DOI: 10.1002/chin.200937054 |
0.355 |
|
| 2008 |
He P, Dong CG, Hu QS. Synthesis of hindered biphenyls by sequential non-transition metal-catalyzed reaction/palladium-catalyzed cross-couplings. Tetrahedron Letters. 49: 1906-1909. PMID 19295906 DOI: 10.1016/J.Tetlet.2008.01.101 |
0.591 |
|
| 2008 |
Dong CG, Hu QS. Pd(OAc)(2)-catalyzed domino reactions of 1,2-dihaloarenes and 2-haloaryl arenesulfonates with Grignard reagents: efficient synthesis of substituted fluorenes. Tetrahedron. 64: 2537-2552. PMID 19279672 DOI: 10.1016/j.tet.2008.01.020 |
0.42 |
|
| 2008 |
Liao YX, Xing CH, He P, Hu QS. Orthoplatinated triarylphosphite as a highly efficient catalyst for addition reactions of arylboronic acids with aldehydes: low catalyst loading catalysis and a new tandem reaction sequence. Organic Letters. 10: 2509-12. PMID 18465865 DOI: 10.1021/Ol800774C |
0.706 |
|
| 2008 |
Hu Q, Dong C, Liu T. Synthesis of Substituted Indenes andcis-Stilbenoid Hydrocarbons via Palladium-Catalyzed Domino Reactions of Hindered Grignard Reagents with (E)-1,2-Dibromoethenes Synthesis. 2008: 2650-2658. DOI: 10.1055/s-2008-1067195 |
0.459 |
|
| 2008 |
Dong C, Liu T, Hu Q. ChemInform Abstract: Synthesis of Substituted Indenes and cis-Stilbenoid Hydrocarbons via Palladium-Catalyzed Domino Reactions of Hindered Grignard Reagents with (E)-1,2-Dibromoethenes. Cheminform. 39. DOI: 10.1002/chin.200852104 |
0.408 |
|
| 2008 |
Dong C, Hu Q. ChemInform Abstract: Pd(OAc)2-Catalyzed Domino Reactions of 1,2-Dihaloarenes and 2-Haloaryl Arenesulfonates with Grignard Reagents: Efficient Synthesis of Substituted Fluorenes. Cheminform. 39. DOI: 10.1002/CHIN.200834100 |
0.396 |
|
| 2008 |
He P, Dong C, Hu Q. ChemInform Abstract: Synthesis of Hindered Biphenyls by Sequential Non-Transition Metal-Catalyzed Reaction/Palladium-Catalyzed Cross-Couplings. Cheminform. 39. DOI: 10.1002/CHIN.200826095 |
0.413 |
|
| 2007 |
He P, Lu Y, Hu QS. Phosphinite- and phosphite-based Type I palladacycles as highly active catalysts for addition reactions of arylboronic acids with aldehydes, α,β-unsaturated ketones, α-ketoesters, and aldimines. Tetrahedron Letters. 48: 5283-5288. PMID 18648490 DOI: 10.1016/J.Tetlet.2007.05.119 |
0.474 |
|
| 2007 |
Dong CG, Yeung P, Hu QS. Two palladium-catalyzed domino reactions from one set of substrates/reagents: efficient synthesis of substituted indenes and cis-stilbenoid hydrocarbons from the same internal alkynes and hindered Grignard reagents. Organic Letters. 9: 363-6. PMID 17217305 DOI: 10.1021/ol062885a |
0.492 |
|
| 2007 |
He P, Lu Y, Dong CG, Hu QS. Anionic four-electron donor-based palladacycles as catalysts for addition reactions of arylboronic acids with alpha,beta-unsaturated ketones, aldehydes, and alpha-ketoesters. Organic Letters. 9: 343-6. PMID 17217300 DOI: 10.1021/Ol062814B |
0.508 |
|
| 2007 |
Hu Q. Controlling Competing Pathways in Palladium-Catalyzed Tandem/Domino Reactions of Hindered Grignard Reagents with 1,2-Dihaloarenes and 2-Haloaryl Tosylates Synlett. 2007: 1331-1345. DOI: 10.1055/s-2007-980347 |
0.431 |
|
| 2007 |
He P, Lu Y, Hu Q. Phosphinite- and Phosphite-Based Type I Palladacycles as Highly Active Catalysts for Addition Reactions of Arylboronic Acids with Aldehydes, α,β-Unsaturated Ketones, α-Ketoesters, and Aldimines. Cheminform. 38. DOI: 10.1002/CHIN.200745088 |
0.393 |
|
| 2007 |
Hu Q. Controlling Competing Pathways in Palladium-Catalyzed Tandem/Domino Reactions of Hindered Grignard Reagents with 1,2-Dihaloarenes and 2-Haloaryl Tosylates Cheminform. 38. DOI: 10.1002/chin.200735252 |
0.431 |
|
| 2007 |
He P, Lu Y, Dong C, Hu Q. Anionic Four-Electron Donor-Based Palladacycles as Catalysts for Addition Reactions of Arylboronic Acids with α,β-Unsaturated Ketones, Aldehydes, and α-Ketoesters. Cheminform. 38. DOI: 10.1002/chin.200720086 |
0.379 |
|
| 2007 |
Dong C, Yeung P, Hu Q. Two Palladium-Catalyzed Domino Reactions from One Set of Substrates/Reagents: Efficient Synthesis of Substituted Indenes and cis-Stilbenoid Hydrocarbons from the Same Internal Alkynes and Hindered Grignard Reagents. Cheminform. 38. DOI: 10.1002/chin.200718097 |
0.435 |
|
| 2007 |
Dong C, Hu Q. Pd(OAc)2-Catalyzed Domino Reactions of 1-Chloro-2-haloarenes and 2-Haloaryl Tosylates with Hindered Grignard Reagents via Palladium-Associated Arynes. Cheminform. 38. DOI: 10.1002/chin.200708095 |
0.346 |
|
| 2006 |
Dong CG, Hu QS. Pd(OAc)(2)-catalyzed Domino reactions of 1-chloro-2-haloarenes and 2-haloaryl tosylates with hindered Grignard reagents via palladium-associated arynes. Organic Letters. 8: 5057-60. PMID 17048842 DOI: 10.1021/ol061989i |
0.435 |
|
| 2006 |
Dong CG, Hu QS. Annulative tandem reactions based on Pd0/tBu3P-catalyzed cross-coupling and C(sp3)-H bond activation. Angewandte Chemie (International Ed. in English). 45: 2289-92. PMID 16518774 DOI: 10.1002/Anie.200504310 |
0.401 |
|
| 2006 |
Tang ZY, Hu QS. Triphenylphosphine as a ligand for room-temperature Ni(0)-catalyzed cross-coupling reactions of aryl chlorides with arylboronic acids. The Journal of Organic Chemistry. 71: 2167-9. PMID 16497011 DOI: 10.1021/Jo052369I |
0.541 |
|
| 2006 |
Tang Z, Spinella S, Hu Q. Ferrocenylmethylphosphines as ligands for room temperature Ni(0)-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl arenesulfonates and aryl chlorides Tetrahedron Letters. 47: 2427-2430. DOI: 10.1016/j.tetlet.2006.01.145 |
0.404 |
|
| 2006 |
Tang Z, Spinella S, Hu Q. Ferrocenylmethylphosphines as Ligands for Room Temperature Ni(0)-Catalyzed Suzuki—Miyaura Cross-Coupling Reactions of Aryl Arenesulfonates and Aryl Chlorides. Cheminform. 37. DOI: 10.1016/J.Tetlet.2006.01.145 |
0.457 |
|
| 2006 |
Tang Z, Hu Q. Efficient Synthesis of 2-Substituted Indoles Based on Palladium(II) Acetate/Tri-tert-butylphosphine-Catalyzed Alkynylation/Amination of 1,2-Dihalobenzenes. Cheminform. 37. DOI: 10.1002/chin.200637106 |
0.357 |
|
| 2006 |
Tang Z, Hu Q. Triphenylphosphine as a Ligand for Room-Temperature Ni(0)-Catalyzed Cross-Coupling Reactions of Aryl Chlorides with Arylboronic Acids. Cheminform. 37. DOI: 10.1002/chin.200629076 |
0.441 |
|
| 2006 |
Tang Z, Hu Q. Efficient Synthesis of 2-Substituted Indoles Based on Palladium(II) Acetate/Tri-tert-butylphosphine-Catalyzed Alkynylation/Amination of 1,2-Dihalobenzenes Advanced Synthesis & Catalysis. 348: 846-850. DOI: 10.1002/Adsc.200606022 |
0.506 |
|
| 2006 |
Lu Y, Plocher E, Hu Q. Synthesis of Novel Bisphosphine-Containing Polymers and Their Applications as Bidentate Ligands for Nickel(0)-Catalyzed Cross-Coupling Reactions Advanced Synthesis & Catalysis. 348: 841-845. DOI: 10.1002/adsc.200606002 |
0.375 |
|
| 2006 |
Lu Y, Plocher E, Hu Q. Synthesis of Novel Bisphosphine-Containing Polymers and Their Applications as Bidentate Ligands for Nickel(0)-Catalyzed Cross-Coupling Reactions. Cheminform. 37. DOI: 10.1002/Adsc.200606002 |
0.496 |
|
| 2005 |
Dong CG, Hu QS. Preferential oxidative addition in palladium(0)-catalyzed suzuki cross-coupling reactions of dihaloarenes with arylboronic acids. Journal of the American Chemical Society. 127: 10006-7. PMID 16011357 DOI: 10.1021/Ja052547P |
0.475 |
|
| 2005 |
Dong C, Hu Q. Preferential Oxidative Addition in Palladium(0)-Catalyzed Suzuki Cross-Coupling Reactions of Dihaloarenes with Arylboronic Acids. Cheminform. 36. DOI: 10.1002/chin.200548102 |
0.452 |
|
| 2004 |
Tang ZY, Hu QS. Room-temperature Ni0-catalyzed cross-coupling reactions of aryl arenesulfonates with arylboronic acids. Journal of the American Chemical Society. 126: 3058-9. PMID 15012129 DOI: 10.1021/Ja038752R |
0.554 |
|
| 2004 |
Tang Z, Hu Q. Room-Temperature Ni(0)-Catalyzed Cross-Coupling Reactions of Aryl Arenesulfonates with Arylboronic Acids. Cheminform. 35. DOI: 10.1002/chin.200428107 |
0.439 |
|
| 2004 |
Tang Z, Hu Q. Room Temperature Nickel(0)-Catalyzed Suzuki-Miyaura Cross-Couplings of Activated Alkenyl Tosylates: Efficient Synthesis of 4-Substituted Coumarins and 4-Substituted 2(5H)- Furanones Advanced Synthesis & Catalysis. 346: 1635-1637. DOI: 10.1002/Adsc.200404150 |
0.48 |
|
| 2003 |
Hu QS, Lu Y, Tang ZY, Yu HB. Macromolecular effect: synthesis of a ferrocenylmethylphosphine-containing polymer as highly efficient ligands for room-temperature palladium(0)-catalyzed Suzuki cross-coupling reactions of aryl chlorides. Journal of the American Chemical Society. 125: 2856-7. PMID 12617635 DOI: 10.1021/Ja029021E |
0.467 |
|
| 2003 |
Tang ZY, Lu Y, Hu QS. Direct synthesis of ferrocenylmethylphosphines from ferrocenylmethyl alcohols and their application as ligands for room temperature Pd(0)-catalyzed Suzuki cross-couplings of aryl bromides. Organic Letters. 5: 297-300. PMID 12556176 DOI: 10.1021/Ol0272601 |
0.472 |
|
| 2003 |
Jayaprakash D, Kobayashi Y, Arai T, Hu QS, Zheng XF, Pu L, Sasai H. Catalytic asymmetric epoxidation of α,β-unsaturated ketones using polymeric BINOL Journal of Molecular Catalysis a: Chemical. 196: 145-149. DOI: 10.1016/S1381-1169(02)00644-1 |
0.342 |
|
| 2003 |
Hu Q, Lu Y, Tang Z, Yu H. Macromolecular Effect: Synthesis of a Ferrocenylmethylphosphine-Containing Polymer as Highly Efficient Ligands for Room-Temperature Palladium(0)-Catalyzed Suzuki Cross-Coupling Reactions of Aryl Chlorides. Cheminform. 34. DOI: 10.1002/chin.200328104 |
0.407 |
|
| 2002 |
Hu QS, Sun C, Monaghan CE. Optically active dendronized polymers as a new type of macromolecular chiral catalysts for asymmetric catalysis Tetrahedron Letters. 43: 927-930. DOI: 10.1016/S0040-4039(01)02300-0 |
0.374 |
|
| 2001 |
Hu QS, Sun C, Monaghan CE. Synthesis of optically active polymers with chiral units attached to rigid backbones and their application for asymmetric catalysis Tetrahedron Letters. 42: 7725-7728. DOI: 10.1016/S0040-4039(01)01689-6 |
0.383 |
|
| 1999 |
Johannsen M, Jørgensen KA, Zheng XF, Hu QS, Pu L. A Highly Enantioselective Hetero-Diels-Alder Reaction Catalyzed by Chiral Polybinaphthyl-Aluminum Complexes. The Journal of Organic Chemistry. 64: 299-301. PMID 11674119 DOI: 10.1021/Jo981466R |
0.443 |
|
| 1997 |
Hu Q, Huang W, Vitharana D, Zheng X, Pu L. Functionalized Major-Groove and Minor-Groove Chiral Polybinaphthyls: Application in the Asymmetric Reaction of Aldehydes with Diethylzinc Journal of the American Chemical Society. 119: 12454-12464. DOI: 10.1021/ja972623r |
0.402 |
|
| 1997 |
Hu Q, Hu C. Reformatsky reactions of ethyl 4,4-difluoro-3-ethoxy-4-halocrotonates: synthesis of 4,4-difluorocarbonate derivatives and 2-lactenones Journal of Fluorine Chemistry. 83: 87-88. DOI: 10.1016/S0022-1139(97)00013-4 |
0.462 |
|
| 1996 |
Hu Q, Vitharana D, Zheng X, Wu C, Kwan CMS, Pu L. Poly(1,1‘-bi-2-naphthol)s: Synthesis, Characterization, and Application in Lewis Acid Catalysis The Journal of Organic Chemistry. 61: 8370-8377. DOI: 10.1021/jo961407i |
0.311 |
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| Show low-probability matches. |