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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