Hongli Bao - Publications

Affiliations: 
Chemistry University of Texas Southwestern Medical Center, Dallas, TX, United States 

73 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
2023 Ye C, Huang R, Chiou MF, Wang B, Li D, Bao H. Synthesis of a new fluorophore: wavelength-tunable bisbenzo[]isoindolylidenes. Chemical Science. 14: 13151-13158. PMID 38023512 DOI: 10.1039/d3sc04445a  0.304
2023 Xue M, Cui J, Zhu X, Wang F, Lv D, Nie Z, Li Y, Bao H. Copper-Catalyzed Radical Enantioselective Synthesis of γ-Butyrolactones with Two Non-vicinal Carbon Stereocenters. Angewandte Chemie (International Ed. in English). e202304275. PMID 37170440 DOI: 10.1002/anie.202304275  0.338
2022 Li Y, Bao H. Radical transformations for allene synthesis. Chemical Science. 13: 8491-8506. PMID 35974759 DOI: 10.1039/d2sc02573f  0.319
2022 Li T, Chiou MF, Li Y, Ye C, Su M, Xue M, Yuan X, Wang C, Wan WM, Li D, Bao H. Synthesis of unsymmetrically tetrasubstituted pyrroles and studies of AIEE in pyrrolo[1,2-]pyrimidine derivatives. Chemical Science. 13: 5667-5673. PMID 35694357 DOI: 10.1039/d2sc00837h  0.375
2022 Nie Z, Chiou MF, Cui J, Qu Y, Zhu X, Jian W, Xiong H, Li Y, Bao H. Copper-catalyzed radical enantioselective carbo-esterification of styrenes enabled by a perfluoroalkylated-PyBox ligand. Angewandte Chemie (International Ed. in English). PMID 35510403 DOI: 10.1002/anie.202202077  0.375
2021 Zhu X, Jian W, Huang M, Li D, Li Y, Zhang X, Bao H. Asymmetric radical carboesterification of dienes. Nature Communications. 12: 6670. PMID 34795235 DOI: 10.1038/s41467-021-26843-2  0.331
2021 Wang K, Li Y, Li X, Li D, Bao H. Iron-Catalyzed Asymmetric Decarboxylative Azidation. Organic Letters. 23: 8847-8851. PMID 34755516 DOI: 10.1021/acs.orglett.1c03355  0.404
2021 Ye C, Jiao Y, Chiou MF, Li Y, Bao H. Direct synthesis of pentasubstituted pyrroles and hexasubstituted pyrrolines from propargyl sulfonylamides and allenamides. Chemical Science. 12: 9162-9167. PMID 34276946 DOI: 10.1039/d1sc02090k  0.37
2021 Ye C, Jiao Y, Chiou MF, Li Y, Bao H. Direct synthesis of pentasubstituted pyrroles and hexasubstituted pyrrolines from propargyl sulfonylamides and allenamides. Chemical Science. 12: 9162-9167. PMID 34276946 DOI: 10.1039/d1sc02090k  0.37
2021 Cao J, Lv D, Yu F, Chiou MF, Li Y, Bao H. Regioselective Three-Component Synthesis of Vicinal Diamines via 1,2-Diamination of Styrenes. Organic Letters. PMID 33792337 DOI: 10.1021/acs.orglett.1c00898  0.374
2021 Bao H, Lv D, Sun Q, Zhou H, Ge L, Qu Y, Li T, Ma X, Li Y. Iron-Catalyzed Radical Asymmetric Aminoazidation and Diazidation of Styrenes. Angewandte Chemie (International Ed. in English). PMID 33749966 DOI: 10.1002/anie.202017175  0.401
2020 Zeng Y, Chiou MF, Zhu X, Cao J, Lv D, Jian W, Li Y, Zhang X, Bao H. Copper-Catalyzed Enantioselective Radical 1,4-Difunctionalization of 1,3-Enynes. Journal of the American Chemical Society. PMID 33035049 DOI: 10.1021/jacs.0c06177  0.411
2020 Zhang Q, Muhammad MT, Chiou MF, Jiao Y, Bao H, Li Y. 1,4-Fluoroamination of 1,3-Enynes en Route to Fluorinated Allenes. Organic Letters. 22: 5261-5265. PMID 32610936 DOI: 10.1021/Acs.Orglett.0C01953  0.401
2020 Li SS, Zhu N, Jing YN, Li Y, Bao H, Wan WM. Barbier Self-Condensing Ketyl Polymerization-Induced Emission: A Polarity Reversal Approach to Reversed Polymerizability. Iscience. 23: 101031. PMID 32299054 DOI: 10.1016/J.Isci.2020.101031  0.311
2020 Wei R, Xiong H, Ye C, Li Y, Bao H. Iron-Catalyzed Alkylazidation of 1,1-Disubstituted Alkenes with Diacylperoxides and TMSN. Organic Letters. PMID 32227900 DOI: 10.1021/Acs.Orglett.0C00969  0.446
2020 Chiou MF, Xiong H, Li Y, Bao H, Zhang X. Revealing the Iron-Catalyzed β-Methyl Scission of -Butoxyl Radicals via the Mechanistic Studies of Carboazidation of Alkenes. Molecules (Basel, Switzerland). 25. PMID 32182775 DOI: 10.3390/Molecules25051224  0.331
2020 Zhu N, Chiou MF, Xiong H, Su M, Su M, Li Y, Wan WM, Bao H. The Introduction of the Radical Cascade Reaction into Polymer Chemistry: A One-Step Strategy for Synchronized Polymerization and Modification. Iscience. 23: 100902. PMID 32106054 DOI: 10.1016/J.Isci.2020.100902  0.362
2020 Zhu N, Su M, Wan WM, Li Y, Bao H. Practical Method for Reductive Deuteration of Ketones with Magnesium and DO. Organic Letters. PMID 31967845 DOI: 10.1021/Acs.Orglett.9B04536  0.329
2020 Taj Muhammad M, Jiao Y, Ye C, Chiou MF, Israr M, Zhu X, Li Y, Wen Z, Studer A, Bao H. Synthesis of difluoromethylated allenes through trifunctionalization of 1,3-enynes. Nature Communications. 11: 416. PMID 31964875 DOI: 10.1038/S41467-019-14254-3  0.471
2020 Israr M, Xiong H, Li Y, Bao H. Copper‐Catalyzed Enantioselective Cyano(Fluoro)Alkylation of Alkenes Advanced Synthesis & Catalysis. 362: 2211-2215. DOI: 10.1002/Adsc.202000230  0.503
2019 Zhu X, Su M, Zhang Q, Li Y, Bao H. Cu-Catalyzed Alkylarylation of Vinylarenes with Masked Alkyl Electrophiles. Organic Letters. PMID 31855441 DOI: 10.1021/Acs.Orglett.9B04392  0.463
2019 Israr M, Xiong H, Li Y, Bao H. Copper(I)-Catalyzed Cyanoperfluoroalkylation of Alkynes. Organic Letters. PMID 31436436 DOI: 10.1021/Acs.Orglett.9B02648  0.511
2019 Ye C, Li Y, Zhu X, Hu S, Yuan D, Bao H. Copper-catalyzed 1,4-alkylarylation of 1,3-enynes with masked alkyl electrophiles. Chemical Science. 10: 3632-3636. PMID 30996957 DOI: 10.1039/C8Sc05689G  0.525
2019 Xiong H, Li Y, Qian B, Wei R, Van der Eycken EV, Bao H. Iron(II)-Catalyzed Heck-Type Coupling of Vinylarenes with Alkyl Iodides. Organic Letters. PMID 30668128 DOI: 10.1021/Acs.Orglett.8B04024  0.424
2019 Xiong H, Ramkumar N, Chiou MF, Jian W, Li Y, Su JH, Zhang X, Bao H. Iron-catalyzed carboazidation of alkenes and alkynes. Nature Communications. 10: 122. PMID 30631054 DOI: 10.1038/S41467-018-07985-2  0.468
2019 Wei R, Ge L, Bao H, Liao S, Li Y. Copper-Catalyzed Nitrogenation of Aromatic and Aliphatic Aldehydes: A Direct Route to Carbamoyl Azides Synthesis. 51: 4645-4649. DOI: 10.1055/S-0039-1690683  0.519
2019 Jiao Y, Chiou M, Li Y, Bao H. Copper-Catalyzed Radical Acyl-Cyanation of Alkenes with Mechanistic Studies on the tert-Butoxy Radical Acs Catalysis. 9: 5191-5197. DOI: 10.1021/Acscatal.9B01060  0.401
2018 Ge L, Li Y, Bao H. Iron-Catalyzed Radical Acyl-Azidation of Alkenes with Aldehydes: Synthesis of Unsymmetrical β-Azido Ketones. Organic Letters. PMID 30582706 DOI: 10.1021/Acs.Orglett.8B03688  0.424
2018 Deng W, Ye C, Li Y, Li D, Bao H. Iron-Catalyzed Oxyalkylation of Terminal Alkynes with Alkyl Iodides. Organic Letters. PMID 30582704 DOI: 10.1021/Acs.Orglett.8B03689  0.469
2018 Israr M, Ye C, Muhammad MT, Li Y, Bao H. Copper(I)-catalyzed tandem reaction: synthesis of 1,4-disubstituted 1,2,3-triazoles from alkyl diacyl peroxides, azidotrimethylsilane, and alkynes. Beilstein Journal of Organic Chemistry. 14: 2916-2922. PMID 30546475 DOI: 10.3762/Bjoc.14.270  0.537
2018 Zhu X, Deng W, Chiou MF, Ye C, Jian W, Zeng Y, Jiao Y, Ge L, Li Y, Zhang X, Bao H. Copper-Catalyzed Radical 1,4-Difunctionalization of 1,3-Enynes with Alkyl Diacyl Peroxides and N-fluorobenzenesulfonimide. Journal of the American Chemical Society. PMID 30509065 DOI: 10.1021/Jacs.8B11499  0.456
2018 Zhou H, Ge L, Song J, Jian W, Li Y, Li C, Bao H. HOTf-Catalyzed Alkyl-Heck-type Reaction. Iscience. 3: 255-263. PMID 30428325 DOI: 10.1016/J.Isci.2018.04.020  0.451
2018 Bao H, Wan WM, Tian D, Jing YN, Zhang XY, Wu W, Ren H. NBN Doped Conjugated Polycyclic Aromatic Hydrocarbons as a New Class of AIEgen for Extremely Sensitive Explosive Detection. Angewandte Chemie (International Ed. in English). PMID 30255542 DOI: 10.1002/Anie.201809844  0.348
2018 Deng W, Feng W, Li Y, Bao H. Merging Visible-Light Photocatalysis and Transition-Metal Catalysis in Three-Component Alkyl-Fluorination of Olefins with a Fluoride Ion. Organic Letters. PMID 29956940 DOI: 10.1021/Acs.Orglett.8B01658  0.468
2018 Ye C, Qian B, Li Y, Su M, Li D, Bao H. Iron-Catalyzed Dehydrative Alkylation of Propargyl Alcohol with Alkyl Peroxides To Form Substituted 1,3-Enynes. Organic Letters. PMID 29786445 DOI: 10.1021/Acs.Orglett.8B01043  0.493
2018 Bao H, Ge L, Jian W, Zhou H, Chen S, Ye C, Yu F, Qian B, Li Y. Iron-Catalyzed Vinylic C-H Alkylation with Alkyl Peroxides. Chemistry, An Asian Journal. PMID 29767475 DOI: 10.1002/Asia.201800534  0.478
2018 Qian B, Bao H, Zeng Y, Li Y. A Metal-Free Approach for Brønsted Acid Promoted C–H Alkyl­ation of Heteroarenes with Alkyl Peroxides Synthesis. 50: 3250-3256. DOI: 10.1055/S-0037-1609965  0.453
2018 Li Y, Bao H, Deng W, Li Y. Iron-Catalyzed Carboiodination of Alkynes Synthesis. 50: 2974-2980. DOI: 10.1055/S-0037-1609448  0.461
2018 Zhu X, Qian B, Wei R, Huang J, Bao H. Correction: Protection of COOH and OH groups in acid, base and salt free reactions Green Chemistry. 20: 2664-2665. DOI: 10.1039/C8Gc90046A  0.312
2018 Zhu X, Qian B, Wei R, Huang J, Bao H. Protection of COOH and OH groups in acid, base and salt free reactions Green Chemistry. 20: 1444-1447. DOI: 10.1039/C8Gc00037A  0.417
2017 Yu F, Wang T, Zhou H, Li Y, Zhang X, Bao H. Iron(III)-Catalyzed Ortho-Preferred Radical Nucleophilic Alkylation of Electron-Deficient Arenes. Organic Letters. 19: 6538-6541. PMID 29190111 DOI: 10.1021/Acs.Orglett.7B03244  0.452
2017 Zhou H, Jian W, Qian B, Ye C, Li D, Zhou J, Bao H. Copper-Catalyzed Ligand-Free Diazidation of Olefins with TMSN3 in CH3CN or in H2O. Organic Letters. PMID 29090941 DOI: 10.1021/Acs.Orglett.7B02982  0.435
2017 Zhu N, Wang T, Ge L, Li Y, Zhang X, Bao H. γ-Amino Butyric Acid (GABA) Synthesis Enabled by Copper-Catalyzed Carboamination of Alkenes. Organic Letters. PMID 28862865 DOI: 10.1021/Acs.Orglett.7B01969  0.379
2017 Qian B, Chen S, Wang T, Zhang X, Bao H. Iron-Catalyzed Carboamination of Olefins: Synthesis of Amines and Disubstituted β-Amino Acids. Journal of the American Chemical Society. PMID 28857555 DOI: 10.1021/Jacs.7B06590  0.48
2017 Ge L, Li Y, Jian W, Bao H. Alkyl-Esterification of Vinylarenes Enabled by Visible-Light Induced Decarboxylation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28681966 DOI: 10.1002/Chem.201702385  0.465
2017 Zhu X, Ye C, Li Y, Bao H. Iron-Catalyzed Radical Decarboxylative Oxyalkylation of Terminal Alkynes with Alkyl Peroxides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28627009 DOI: 10.1002/Chem.201701830  0.495
2017 Zhu N, Zhao J, Bao H. Iron catalyzed methylation and ethylation of vinyl arenes. Chemical Science. 8: 2081-2085. PMID 28451327 DOI: 10.1039/C6Sc04274K  0.464
2017 Jian W, Ge L, Jiao Y, Qian B, Bao H. Iron-Catalyzed Decarboxylative Alkyl Etherification of Vinylarenes with Aliphatic Acids as the Alkyl Source. Angewandte Chemie (International Ed. in English). PMID 28230308 DOI: 10.1002/Anie.201612365  0.47
2017 Babu KR, Chen S, Li Y, Bao H. Iron Catalyzed Oxidative Hydroarylation, Methylarylation, and Diarylation of Vinylarenes to Generate Unsymmetrical 1,1-Diarylalkanes Chinese Journal of Organic Chemistry. 37: 1160. DOI: 10.6023/Cjoc201702036  0.389
2017 Bao H, Li Y, Ge L, Muhammad M. Recent Progress on Radical Decarboxylative Alkylation for Csp3–C Bond Formation Synthesis. 49: 5263-5284. DOI: 10.1055/S-0036-1590935  0.387
2017 Zhu N, Qian B, Xiong H, Bao H. Copper-catalyzed regioselective allylic oxidation of olefins via C–H activation Tetrahedron Letters. 58: 4125-4128. DOI: 10.1016/J.Tetlet.2017.09.047  0.487
2017 Jian W, Qian B, Bao H, Li D. AlCl3 catalyzed oxa-Diels-Alder reaction of aromatic aldehydes with simple dienes Tetrahedron. 73: 4039-4044. DOI: 10.1016/J.Tet.2016.10.049  0.474
2017 Ye C, Li Y, Bao H. Copper-Catalyzed Decarboxylative Alkylation of Terminal Alkynes Advanced Synthesis & Catalysis. 359: 3720-3724. DOI: 10.1002/Adsc.201700798  0.505
2016 Babu KR, Zhu N, Bao H. Iron-Catalyzed C-H Alkylation of Heterocyclic C-H Bonds. Organic Letters. PMID 27936779 DOI: 10.1021/Acs.Orglett.6B03287  0.436
2016 Li Y, Han Y, Xiong H, Zhu N, Qian B, Ye C, Kantchev EA, Bao H. Copper-Catalyzed Regioselective 1,2-Alkylesterification of Dienes to Allylic Esters. Organic Letters. PMID 26790009 DOI: 10.1021/Acs.Orglett.5B03399  0.467
2016 Li Y, Ge L, Qian B, Babu KR, Bao H. Hydroalkylation of terminal aryl alkynes with alkyl diacyl peroxides Tetrahedron Letters. 57: 5677-5680. DOI: 10.1016/J.Tetlet.2016.11.020  0.511
2016 Qian B, Xiong H, Zhu N, Ye C, Jian W, Bao H. Copper-catalyzed diesterification of 1,3-diene for the synthesis of allylic diester compounds Tetrahedron Letters. 57: 3400-3403. DOI: 10.1016/J.Tetlet.2016.06.087  0.493
2016 Qian B, Xiong H, Zhu N, Ye C, Jian W, Bao H. ChemInform Abstract: Copper-Catalyzed Diesterification of 1,3-Diene for the Synthesis of Allylic Diester Compounds. Cheminform. 47. DOI: 10.1002/chin.201646084  0.312
2014 Bao H, Bayeh L, Tambar UK. Regioselective and Diastereoselective Aminoarylation of 1,3-Dienes. Chemical Science (Royal Society of Chemistry : 2010). 5: 4863-4867. PMID 25431651 DOI: 10.1039/C4Sc01152J  0.71
2014 Bao H, Bayeh L, Tambar UK. Allylic functionalization of unactivated olefins with Grignard reagents. Angewandte Chemie (International Ed. in English). 53: 1664-8. PMID 24458538 DOI: 10.1002/Anie.201309134  0.709
2013 Bao H, Bayeh L, Tambar UK. Catalytic Enantioselective Allylic Amination of Olefins for the Synthesis of ent-Sitagliptin. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 24: 2459-2463. PMID 25378809 DOI: 10.1055/S-0033-1340079  0.723
2013 Bao H, Wang Z, You T, Ding K. Enantioselective ring opening of meso-epoxides with aromatic amines catalyzed by dinuclear magnesium complexes Chinese Journal of Chemistry. 31: 67-71. DOI: 10.1002/Cjoc.201201008  0.489
2012 Bao H, Tambar UK. Catalytic enantioselective allylic amination of unactivated terminal olefins via an ene reaction/[2,3]-rearrangement. Journal of the American Chemical Society. 134: 18495-8. PMID 23106555 DOI: 10.1021/Ja307851B  0.725
2011 Qi X, Bao H, Tambar UK. Total synthesis of (±)-trigonoliimine C via oxidative rearrangement of an unsymmetrical bis-tryptamine. Journal of the American Chemical Society. 133: 10050-3. PMID 21671591 DOI: 10.1021/Ja203960B  0.73
2011 Bao H, Qi X, Tambar UK. Catalytic enantioselective [2,3]-rearrangements of amine N-oxides. Journal of the American Chemical Society. 133: 1206-8. PMID 21218772 DOI: 10.1021/Ja110500M  0.766
2011 Bao H, Qi X, Tambar UK. Stereoselective [2,3]-rearrangements of amine N -oxides Synlett. 1789-1792. DOI: 10.1055/S-0030-1260962  0.75
2010 Bao H, Wu J, Li H, Wang Z, You T, Ding K. Enantioselective ring opening reaction of meso-epoxides with aromatic and aliphatic amines catalyzed by magnesium complexes of BINOL derivatives European Journal of Organic Chemistry. 6722-6726. DOI: 10.1002/Ejoc.201001222  0.499
2008 Bao H, Zhou J, Wang Z, Guo Y, You T, Ding K. Insight into the mechanism of the asymmetric ring-opening aminolysis of 4,4-dimethyl-3,5,8-trioxabicyclo[5.1.0]octane catalyzed by titanium/BINOLate/water system: evidence for the Ti(BINOLate)2-bearing active catalyst entities and the role of water. Journal of the American Chemical Society. 130: 10116-27. PMID 18616252 DOI: 10.1021/Ja801847R  0.382
2008 Du H, Zhang X, Wang Z, Bao H, You T, Ding K. BINOlate-magnesium catalysts for enantioselective hetero-Diels-Alder reaction of Danishefsky's diene with aldehydes European Journal of Organic Chemistry. 2248-2254. DOI: 10.1002/Ejoc.200701223  0.453
2005 Li D, Bao H, You T. Microwave-assisted and efficient one-pot synthesis of substituted 1,2,4-triazoles Heterocycles. 65: 1957-1962. DOI: 10.3987/Com-05-10415  0.447
2005 Li D, Bao H, Tan Q, Cai D, You T. Synthesis of ribavirin analogues containing amino-acid residues Synthetic Communications. 35: 1017-1026. DOI: 10.1081/Scc-200054185  0.371
2005 Li DL, Bao HL, Tan QT, Ke YP, You TP. Synthesis and biological evaluation of a new category of purine-nucleoside analogues Chinese Journal of Chemistry. 23: 1659-1664. DOI: 10.1002/Cjoc.200591659  0.336
2004 Tan Q, Li D, Bao H, Wang Y, Wen J, You T. A convenient preparation of enantiopure endo-2-hydroxyepicamphor and endo-3-hydroxycamphor from camphoric acid Synthetic Communications. 34: 2945-2950. DOI: 10.1081/Scc-200026645  0.375
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