Xiaodan Zhao, Ph.D. - Publications

Affiliations: 
2013- School of Chemistry Sun Yat-sen University, Guangzhou Shi, Guangdong Sheng, China 
Area:
Organocatalysis
Website:
http://ce.sysu.edu.cn/zhaolab/xiaodan/xiaodan.htm

50 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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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