Year |
Citation |
Score |
2024 |
Huang N, Luo J, Liao L, Zhao X. Catalytic Enantioselective Aminative Difunctionalization of Alkenes. Journal of the American Chemical Society. PMID 38425285 DOI: 10.1021/jacs.4c00307 |
0.405 |
|
2023 |
Liang Y, Huang H, Huang N, Liao L, Zhao X. Catalytic Enantioselective Construction of Chiral γ-Azido Nitriles through Nitrile Group-Promoted Electrophilic Reaction of Alkenes. Organic Letters. 25: 6757-6762. PMID 37656917 DOI: 10.1021/acs.orglett.3c02650 |
0.414 |
|
2022 |
Liang Y, Jiao H, Zhang H, Wang YQ, Zhao X. Chiral Chalcogenide-Catalyzed Enantioselective Electrophilic Hydrothiolation of Alkenes. Organic Letters. PMID 36154012 DOI: 10.1021/acs.orglett.2c03009 |
0.366 |
|
2022 |
Liao L, Xu X, Ji J, Zhao X. Asymmetric Intermolecular Iodinative Difunctionalization of Allylic Sulfonamides Enabled by Organosulfide Catalysis: Modular Entry to Iodinated Chiral Molecules. Journal of the American Chemical Society. 144: 16490-16501. PMID 36053004 DOI: 10.1021/jacs.2c05668 |
0.435 |
|
2022 |
Liao L, Zhao X. Indane-Based Chiral Aryl Chalcogenide Catalysts: Development and Applications in Asymmetric Electrophilic Reactions. Accounts of Chemical Research. 55: 2439-2453. PMID 36007167 DOI: 10.1021/acs.accounts.2c00201 |
0.459 |
|
2022 |
Cui FH, Hua Y, Lin YM, Fei J, Gao LH, Zhao X, Xia H. Selective Difunctionalization of Unactivated Aliphatic Alkenes Enabled by a Metal-Metallaaromatic Catalytic System. Journal of the American Chemical Society. PMID 35077158 DOI: 10.1021/jacs.1c12586 |
0.405 |
|
2021 |
Jiang Q, Li H, Zhao X. Catalytic Electrophilic Thiocarbocyclization of Allenes. Organic Letters. 23: 8777-8782. PMID 34709844 DOI: 10.1021/acs.orglett.1c03270 |
0.375 |
|
2020 |
Liao L, An R, Li H, Xu Y, Wu JJ, Zhao X. Catalytic Access to Functionalized Allylic gem-Difluorides via Fluorinative Meyer-Schuster-Like Rearrangement. Angewandte Chemie (International Ed. in English). PMID 32285538 DOI: 10.1002/Ange.202003897 |
0.43 |
|
2020 |
Zhao X, Liang Y, Ji J, Zhang X, Jiang Q, Luo J. Enantioselective Construction of Axially Chiral Amino Sulfide Vinyl Arenes via Chiral Sulfide-Catalyzed Electrophilic Carbothiolation of Alkynes. Angewandte Chemie (International Ed. in English). PMID 31967383 DOI: 10.1002/Anie.201915470 |
0.502 |
|
2019 |
Wei W, Liao L, Qin T, Zhao X. Access to Saturated Thiocyano-Containing Azaheterocycles via Selenide-Catalyzed Regio- and Stereoselective Thiocyanoaminocyclization of Alkenes. Organic Letters. PMID 31525984 DOI: 10.1021/Acs.Orglett.9B02834 |
0.472 |
|
2019 |
Li H, Liao L, Zhao X. Organoselenium-Catalyzed Aza-Wacker Reactions: Efficient Access to Isoquinolinium Imides and an Isoquinoline N-Oxide Synlett. 30: 1688-1692. DOI: 10.1055/S-0039-1690103 |
0.463 |
|
2019 |
Liang Y, Zhao X. Enantioselective Construction of Chiral Sulfides via Catalytic Electrophilic Azidothiolation and Oxythiolation of N-Allyl Sulfonamides Acs Catalysis. 9: 6896-6902. DOI: 10.1021/Acscatal.9B01900 |
0.48 |
|
2019 |
Cao Q, Luo J, Zhao X. Inside Back Cover: Chiral Sulfide Catalysis for Desymmetrizing Enantioselective Chlorination (Angew. Chem. Int. Ed. 5/2019) Angewandte Chemie. 58: 1519-1519. DOI: 10.1002/Anie.201813898 |
0.4 |
|
2019 |
Cao Q, Luo J, Zhao X. Innenrücktitelbild: Chiral Sulfide Catalysis for Desymmetrizing Enantioselective Chlorination (Angew. Chem. 5/2019) Angewandte Chemie. 131: 1533-1533. DOI: 10.1002/Ange.201813898 |
0.422 |
|
2018 |
Zhao X, Cao Q, Luo J. Chiral Sulfide Catalysis for Desymmetrizing Enantioselective Chlorination. Angewandte Chemie (International Ed. in English). PMID 30456895 DOI: 10.1002/Anie.201811621 |
0.509 |
|
2018 |
Qin T, Jiang Q, Ji J, Luo J, Zhao X. Chiral selenide-catalyzed enantioselective synthesis of trifluoromethylthiolated 2,5-disubstituted oxazolines. Organic & Biomolecular Chemistry. PMID 30427031 DOI: 10.1039/C8Ob02575D |
0.45 |
|
2018 |
Xu J, Zhang Y, Qin T, Zhao X. Catalytic Regio- and Enantioselective Oxytrifluoromethylthiolation of Aliphatic Internal Alkenes by Neighboring Group Assistance. Organic Letters. PMID 30265554 DOI: 10.1021/Acs.Orglett.8B02672 |
0.468 |
|
2018 |
Liu X, Liang Y, Ji J, Luo J, Zhao X. Chiral Selenide-Catalyzed Enantioselective Allylic Reaction and Intermolecular Difunctionalization of Alkenes: Efficient Construction of C-SCF3 Stereogenic Molecules. Journal of the American Chemical Society. PMID 29583000 DOI: 10.1021/Jacs.8B01513 |
0.507 |
|
2018 |
Luo J, Cao Q, Cao X, Zhao X. Selenide-catalyzed enantioselective synthesis of trifluoromethylthiolated tetrahydronaphthalenes by merging desymmetrization and trifluoromethylthiolation. Nature Communications. 9: 527. PMID 29410415 DOI: 10.1038/S41467-018-02955-0 |
0.484 |
|
2018 |
An R, Liao L, Liu X, Song S, Zhao X. Acid-catalyzed oxidative cleavage of S–S and Se–Se bonds with DEAD: efficient access to sulfides and selenides Organic Chemistry Frontiers. 5: 3557-3561. DOI: 10.1039/C8Qo00909K |
0.377 |
|
2018 |
Liao L, Zhang H, Zhao X. Selenium-π-Acid Catalyzed Oxidative Functionalization of Alkynes: Facile Access to Ynones and Multisubstituted Oxazoles Acs Catalysis. 8: 6745-6750. DOI: 10.1021/Acscatal.8B01595 |
0.436 |
|
2018 |
Guo R, Huang J, Zhao X. Organoselenium-Catalyzed Oxidative Allylic Fluorination with Electrophilic N–F Reagent Acs Catalysis. 926-930. DOI: 10.1021/Acscatal.7B03829 |
0.463 |
|
2017 |
Zhu Z, Luo J, Zhao X. Combination of Lewis Basic Selenium Catalysis and Redox Selenium Chemistry: Synthesis of Trifluoromethylthiolated Tertiary Alcohols with Alkenes. Organic Letters. PMID 28876949 DOI: 10.1021/Acs.Orglett.7B02406 |
0.41 |
|
2017 |
Luo J, Liu Y, Zhao X. Chiral Selenide-Catalyzed Enantioselective Construction of Saturated Trifluoromethylthiolated Azaheterocycles. Organic Letters. PMID 28632389 DOI: 10.1021/Acs.Orglett.7B01392 |
0.484 |
|
2017 |
Guo R, Liao L, Zhao X. Electrophilic Selenium Catalysis with Electrophilic N-F Reagents as the Oxidants. Molecules (Basel, Switzerland). 22. PMID 28534837 DOI: 10.3390/Molecules22050835 |
0.348 |
|
2017 |
Liao L, Guo R, Zhao X. Organoselenium-Catalyzed Regioselective C-H Pyridination of 1,3-Dienes and Alkenes. Angewandte Chemie (International Ed. in English). PMID 28090707 DOI: 10.1002/Anie.201610657 |
0.399 |
|
2017 |
Zhao X, Luo J, Liu X. Development of Chalcogenide Catalysts towards Trifluoromethylthiolation Synlett. 28: 397-401. DOI: 10.1055/S-0036-1588926 |
0.462 |
|
2017 |
Liao L, Guo R, Zhao X. Inside Back Cover: Organoselenium‐Catalyzed Regioselective C−H Pyridination of 1,3‐Dienes and Alkenes (Angew. Chem. Int. Ed. 12/2017) Angewandte Chemie. 56: 3393-3393. DOI: 10.1002/Anie.201701294 |
0.342 |
|
2017 |
Liao L, Guo R, Zhao X. Innenrücktitelbild: Organoselenium‐Catalyzed Regioselective C−H Pyridination of 1,3‐Dienes and Alkenes (Angew. Chem. 12/2017) Angewandte Chemie. 129: 3443-3443. DOI: 10.1002/Ange.201701294 |
0.491 |
|
2016 |
Zhao X, Wu JJ, Xu J. Selenide-Catalyzed Stereoselective Construction of Tetrasubstituted Trifluoromethylthiolated Alkenes with Alkynes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27558447 DOI: 10.1002/Chem.201603975 |
0.486 |
|
2016 |
Liu X, An R, Zhang X, Luo J, Zhao X. Enantioselective Trifluoromethylthiolating Lactonization Catalyzed by an Indane-Based Chiral Sulfide. Angewandte Chemie (International Ed. in English). PMID 27027644 DOI: 10.1002/Anie.201601713 |
0.499 |
|
2016 |
Guo R, Huang J, Huang H, Zhao X. Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles. Organic Letters. PMID 26794425 DOI: 10.1021/Acs.Orglett.5B03543 |
0.441 |
|
2016 |
Liu X, An R, Zhang X, Luo J, Zhao X. Inside Back Cover: Enantioselective Trifluoromethylthiolating Lactonization Catalyzed by an Indane-Based Chiral Sulfide (Angew. Chem. Int. Ed. 19/2016) Angewandte Chemie International Edition. 55: 5869-5869. DOI: 10.1002/Anie.201603087 |
0.444 |
|
2016 |
Liu X, An R, Zhang X, Luo J, Zhao X. Innenrücktitelbild: Enantioselective Trifluoromethylthiolating Lactonization Catalyzed by an Indane-Based Chiral Sulfide (Angew. Chem. 19/2016) Angewandte Chemie. 128: 5967-5967. DOI: 10.1002/Ange.201603087 |
0.466 |
|
2015 |
Luo J, Zhu Z, Liu Y, Zhao X. Diaryl Selenide Catalyzed Vicinal Trifluoromethylthioamination of Alkenes. Organic Letters. PMID 26158564 DOI: 10.1021/Acs.Orglett.5B01727 |
0.466 |
|
2015 |
Deng Z, Wei J, Liao L, Huang H, Zhao X. Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: efficient synthesis of 3-amino allylic alcohols. Organic Letters. 17: 1834-7. PMID 25849818 DOI: 10.1021/Acs.Orglett.5B00213 |
0.396 |
|
2015 |
Zhang X, Guo R, Zhao X. Organoselenium-catalyzed synthesis of indoles through intramolecular C–H amination Organic Chemistry Frontiers. 2: 1334-1337. DOI: 10.1039/C5Qo00179J |
0.515 |
|
2013 |
Zhao X, Glover GS, Oberg KM, Dalton DM, Rovis T. SNAr-Derived Decomposition By-products Involving Pentafluorophenyl Triazolium Carbenes. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 24. PMID 24379522 DOI: 10.1055/S-0033-1338842 |
0.662 |
|
2012 |
Zhao X, Ruhl KE, Rovis T. N-heterocyclic-carbene-catalyzed asymmetric oxidative hetero-Diels-Alder reactions with simple aliphatic aldehydes. Angewandte Chemie (International Ed. in English). 51: 12330-3. PMID 23124903 DOI: 10.1002/Anie.201206490 |
0.668 |
|
2011 |
Zhao X, DiRocco DA, Rovis T. N-heterocyclic carbene and Brønsted acid cooperative catalysis: asymmetric synthesis of trans-γ-lactams. Journal of the American Chemical Society. 133: 12466-9. PMID 21780842 DOI: 10.1021/Ja205714G |
0.717 |
|
2011 |
Zhao X, Dong VM. Carbon-sulfur reductive elimination from palladium(IV) sulfinate complexes. Angewandte Chemie (International Ed. in English). 50: 932-4. PMID 21246694 DOI: 10.1002/Anie.201005489 |
0.574 |
|
2010 |
Zhao X, Yeung CS, Dong VM. Palladium-catalyzed ortho-arylation of O-phenylcarbamates with simple arenes and sodium persulfate. Journal of the American Chemical Society. 132: 5837-44. PMID 20359220 DOI: 10.1021/Ja100783C |
0.689 |
|
2010 |
Yeung CS, Zhao X, Borduas N, Dong VM. Pd-catalyzed ortho-arylation of phenylacetamides, benzamides, and anilides with simple arenes using sodium persulfate Chemical Science. 1: 331-336. DOI: 10.1039/C0Sc00231C |
0.699 |
|
2009 |
Zhao X, Dimitrijevi? E, Dong VM. Palladium-catalyzed C-H bond functionalization with arylsulfonyl chlorides. Journal of the American Chemical Society. 131: 3466-7. PMID 19243177 DOI: 10.1021/Ja900200G |
0.627 |
|
2008 |
Zhao X, Yu Z. Rhodium-catalyzed regioselective C-H functionalization via decarbonylation of acid chlorides and C-H bond activation under phosphine-free conditions. Journal of the American Chemical Society. 130: 8136-7. PMID 18540607 DOI: 10.1021/Ja803154H |
0.382 |
|
2007 |
Zhao X, Yu Z, Xu T, Wu P, Yu H. Novel Brønsted acid catalyzed three-component alkylations of indoles with N-phenylselenophthalimide and styrenes. Organic Letters. 9: 5263-6. PMID 17994757 DOI: 10.1021/Ol7024795 |
0.47 |
|
2006 |
Zhao X, Alper H, Yu Z. Stereoselective hydroxycarbonylation of vinyl bromides to alpha,beta-unsaturated carboxylic acids in the ionic liquid [BMIM]PF6. The Journal of Organic Chemistry. 71: 3988-90. PMID 16674081 DOI: 10.1021/jo052651p |
0.381 |
|
2005 |
Zhao X, Yu Z, Yan S, Wu S, Liu R, He W, Wang L. Ruthenium(III) chloride catalyzed efficient synthesis of unsymmetrical diorganyl selenides via cleavage of dibenzyl and diphenyl diselenides in the presence of zinc. The Journal of Organic Chemistry. 70: 7338-41. PMID 16122256 DOI: 10.1021/Jo051015O |
0.448 |
|
2005 |
Zhao X, Yu Z, Zeng F, Chen J, Wu X, Wu S, Xiao W, Zheng Z. Highly Efficient Route to Diselenides from the Reactions of Imines and Selenium in the Presence of Carbon Monoxide and Water Advanced Synthesis & Catalysis. 347: 877-882. DOI: 10.1002/Adsc.200404380 |
0.431 |
|
2004 |
Chen J, Ling G, Yu Z, Wu S, Zhao X, Wu X, Lu S. N‐Arylamides from Selenium‐Catalyzed Reactions of Nitroaromatics and Amides in the Presence of Carbon Monoxide and Mixed Organic Bases Advanced Synthesis & Catalysis. 346: 1267-1270. DOI: 10.1002/Adsc.200404077 |
0.416 |
|
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