Year |
Citation |
Score |
2019 |
Zhou JS, Qin X, Wu C, Hirao H, Moeljadi AMP. Copper-Catalyzed Asymmetric Arylation of N-Heteroaryl Aldimines via an Elementary Step of 1,4-Insertion. Angewandte Chemie (International Ed. in English). PMID 30648341 DOI: 10.1002/anie.201812646 |
0.347 |
|
2018 |
Zhou JS, Zhao X, Xu H, Huang X. Asymmetric Stepwise Reductive Amination of Sulfonamides, Sulfamates and a Phosphinamide via Nickel Catalysis. Angewandte Chemie (International Ed. in English). PMID 30375715 DOI: 10.1002/anie.201809930 |
0.391 |
|
2018 |
Zhou JS, Huang X, Oh WRJJ. Palladium-Catalyzed Enantioselective Arylation of Racemic Ketones to Form Bridged Bicycles via Dynamic Kinetic Resolution. Angewandte Chemie (International Ed. in English). PMID 29709091 DOI: 10.1002/anie.201804318 |
0.367 |
|
2017 |
Zhou JS, Jiao Z, Shi Q. Asymmetric Intermolecular Heck Reaction of Propargylic Acetates and Cycloalkenes to Access Fused Cyclobutenes. Angewandte Chemie (International Ed. in English). PMID 28960756 DOI: 10.1002/anie.201708435 |
0.444 |
|
2017 |
Zhou JS, Yang P, Zhang C, Ma Y, Zhang C, Li A, Tang B. Nickel-Catalyzed N-Alkylation of both Acylhydrazines and Arylamines with Alcohols and Enantioselective Examples. Angewandte Chemie (International Ed. in English). PMID 28960690 DOI: 10.1002/anie.201708949 |
0.3 |
|
2017 |
Zhou JS, Qin X, Lee MWY. Nickel-Catalyzed Asymmetric Reductive Heck Cyclization of Aryl Halides to Access Indolines. Angewandte Chemie (International Ed. in English). PMID 28805280 DOI: 10.1002/anie.201707134 |
0.509 |
|
2017 |
Lei C, Yip YJ, Zhou JS. Nickel-Catalyzed Direct Synthesis of Aryl Olefins from Ketones and Organoboron Reagents under Neutral Conditions. Journal of the American Chemical Society. PMID 28402116 DOI: 10.1021/jacs.7b02742 |
0.37 |
|
2016 |
Jiao Z, Beiger JJ, Jin Y, Ge S, Zhou JS, Hartwig JF. Palladium-Catalyzed Enantioselective α-Arylation of α-Fluoroketones. Journal of the American Chemical Society. 138: 15980-15986. PMID 27960323 DOI: 10.1021/jacs.6b09580 |
0.56 |
|
2016 |
Jiao Z, Chee KW, Zhou JS. Palladium-Catalyzed Asymmetric α-Arylation of Alkylnitriles. Journal of the American Chemical Society. 138: 16240-16243. PMID 27936644 DOI: 10.1021/jacs.6b11610 |
0.317 |
|
2016 |
Lei C, Cao J, Zhou JS. Palladium-Catalyzed Arylation of Ketones and Acetonitrile with Ortho Alkylation of Aryl Rings: De Novo Synthesis of Tetralines and Benzocycloheptenes. Organic Letters. 18: 6120-6123. PMID 27934365 DOI: 10.1021/acs.orglett.6b03130 |
0.545 |
|
2016 |
Yang P, Lim LH, Chuanprasit P, Hirao H, Zhou JS. Nickel-Catalyzed Enantioselective Reductive Amination of Ketones with Both Arylamines and Benzhydrazide. Angewandte Chemie (International Ed. in English). PMID 27572720 DOI: 10.1002/anie.201606821 |
0.41 |
|
2016 |
Wu C, Yue G, Nielsen CD, Xu K, Hirao H, Zhou JS. Asymmetric Conjugate Addition of Organoboron Reagents to Common Enones Using Copper Catalysts. Journal of the American Chemical Society. PMID 26756835 DOI: 10.1021/Jacs.5B11441 |
0.413 |
|
2015 |
Lei C, Jin X, Zhou JS. Palladium-Catalyzed Heteroarylation and Concomitant ortho-Alkylation of Aryl Iodides. Angewandte Chemie (International Ed. in English). PMID 26358935 DOI: 10.1002/anie.201507128 |
0.539 |
|
2015 |
Wu X, Lei C, Yue G, Zhou JS. Palladium-Catalyzed Direct Cyclopropylation of Heterocycles. Angewandte Chemie (International Ed. in English). 54: 9601-5. PMID 26179255 DOI: 10.1002/anie.201504735 |
0.391 |
|
2015 |
Guo S, Yang P, Zhou JS. Nickel-catalyzed asymmetric transfer hydrogenation of conjugated olefins. Chemical Communications (Cambridge, England). 51: 12115-7. PMID 26125068 DOI: 10.1039/c5cc01632k |
0.375 |
|
2014 |
Zou Y, Zhou JS. Palladium-catalyzed intermolecular Heck reaction of alkyl halides. Chemical Communications. 50: 3725-3728. PMID 24577412 DOI: 10.1039/C4Cc00297K |
0.536 |
|
2014 |
Sevov CS, Zhou JS, Hartwig JF. Iridium-catalyzed, intermolecular hydroamination of unactivated alkenes with indoles. Journal of the American Chemical Society. 136: 3200-7. PMID 24483848 DOI: 10.1021/Ja412116D |
0.645 |
|
2014 |
Wu C, Zhou JS. Asymmetric Intermolecular Heck Reaction of Aryl Halides Journal of the American Chemical Society. 136: 650-652. PMID 24383764 DOI: 10.1021/Ja412277Z |
0.599 |
|
2013 |
Liu S, Zhou JS. Desymmetrization of cyclic olefins via asymmetric Heck reaction and hydroarylation. Chemical Communications (Cambridge, England). 49: 11758-60. PMID 24196697 DOI: 10.1039/C3Cc47551D |
0.568 |
|
2013 |
Wu X, Zhou JS. An efficient method for the Heck-Catellani reaction of aryl halides. Chemical Communications (Cambridge, England). 49: 11035-7. PMID 24135960 DOI: 10.1039/C3Cc46381H |
0.513 |
|
2013 |
Qin L, Hirao H, Zhou JS. Regioselective Heck reaction of aliphatic olefins and aryl halides. Chemical Communications (Cambridge, England). 49: 10236-8. PMID 24060852 DOI: 10.1039/C3Cc45911J |
0.559 |
|
2013 |
Hu J, Lu Y, Li Y, Zhou JS. Highly active catalysts of bisphosphine oxides for asymmetric Heck reaction Chemical Communications. 49: 9425-9427. PMID 24005808 DOI: 10.1039/C3Cc45233F |
0.456 |
|
2013 |
Hu J, Hirao H, Li Y, Zhou JS. Palladium-catalyzed asymmetric intermolecular cyclization. Angewandte Chemie (International Ed. in English). 52: 8676-80. PMID 23824841 DOI: 10.1002/Anie.201303753 |
0.6 |
|
2013 |
Wu X, Zhou JS. Selective arylation at the vinylic site of cyclic olefins. Chemical Communications (Cambridge, England). 49: 4794-6. PMID 23609556 DOI: 10.1039/C3Cc41722K |
0.423 |
|
2013 |
Wu X, Lu Y, Hirao H, Zhou JS. Achieving vinylic selectivity in Mizoroki-Heck reaction of cyclic olefins. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 6014-20. PMID 23471848 DOI: 10.1002/Chem.201204427 |
0.56 |
|
2012 |
Yang Z, Zhou JS. Palladium-catalyzed, asymmetric Mizoroki–Heck reaction of benzylic electrophiles using phosphoramidites as chiral ligands Journal of the American Chemical Society. 134: 11833-11835. PMID 22746254 DOI: 10.1021/Ja304099J |
0.571 |
|
2012 |
Zhou JS. Recent developments in asymmetric coupling of enolates Synlett. 2012: 1-5. DOI: 10.1055/S-0031-1290111 |
0.338 |
|
2012 |
Yang J, Liu S, Zheng J, Zhou JS. Room‐Temperature Suzuki–Miyaura Coupling of Heteroaryl Chlorides and Tosylates European Journal of Organic Chemistry. 2012: 6248-6259. DOI: 10.1002/Ejoc.201200918 |
0.493 |
|
2011 |
Huang Z, Liu Z, Zhou JS. An enantioselective, intermolecular α-arylation of ester enolates to form tertiary stereocenters. Journal of the American Chemical Society. 133: 15882-5. PMID 21910505 DOI: 10.1021/Ja2066829 |
0.543 |
|
2008 |
Zhou J, Hartwig JF. Iridium-catalyzed H/D exchange at vinyl groups without olefin isomerization. Angewandte Chemie (International Ed. in English). 47: 5783-7. PMID 18576446 DOI: 10.1002/Anie.200801992 |
0.477 |
|
2003 |
Zhou JS, Fu GC. Cross-couplings of unactivated secondary alkyl halides: room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides. Journal of the American Chemical Society. 125: 14726-7. PMID 14640646 DOI: 10.1021/Ja0389366 |
0.64 |
|
2003 |
Zhou J, Fu GC. Palladium-catalyzed negishi cross-coupling reactions of unactivated alkyl iodides, bromides, chlorides, and tosylates. Journal of the American Chemical Society. 125: 12527-30. PMID 14531697 DOI: 10.1021/Ja0363258 |
0.617 |
|
2000 |
Loh T, Zhou J. A catalytic enantioselective allylation reaction of aldehydes in an aqueous medium Tetrahedron Letters. 41: 5261-5264. DOI: 10.1016/S0040-4039(00)00801-7 |
0.667 |
|
1999 |
Loh T, Zhou J, Li X. An enantioselective indium-mediated allylation reaction of aldehydes and ketones in dichloromethane Tetrahedron Letters. 40: 9333-9336. DOI: 10.1016/S0040-4039(99)01976-0 |
0.651 |
|
1999 |
Loh T, Zhou J. An enantioselective allylation reaction of aldehydes in an aqueous medium Tetrahedron Letters. 40: 9115-9118. DOI: 10.1016/S0040-4039(99)01743-8 |
0.645 |
|
1999 |
Loh T, Zhou J, Li X, Sim K. A novel reductive aminocyclization for the syntheses of chiral pyrrolidines: stereoselective syntheses of (S)-nornicotine and 2-(2′-pyrrolidyl)-pyridines Tetrahedron Letters. 40: 7847-7850. DOI: 10.1016/S0040-4039(99)01606-8 |
0.551 |
|
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