2024:
50)“Vesicle-to-micelle transition in a double chain quaternary ammonium surfactant system: Interfacial behavior and molecular insights”
Gong, J. N., Song, Y., Sun, Y. J., Sun, Q. H., Liu, C. Y. *, Tan, J. J., Li, Z., Xu, B. C.
J. Mol. Liq. 2024, 394, 123714. DOI: 10.1016/j.molliq.2023.123714
2023:
49)“Ethynyl-B(dan) in [3+2] Cycloaddition and Larock Indole Synthesis: Synthesis of Stable Boron-Containing Heteroaromatic Compounds”
Li, J. L., Tanaka, H., Imagawa, T., Tsushima, T., Nakamoto, M., Tan, J. J.*, Yoshida, H.*
Chem. Eur. J., 2023, e202303403. DOI: 10.1002/chem.202303403
48)“Selective S-Arylation of Sulfenamides with Arynes: Access to Sulfilimines”
Guo, Y. F., Zhuang, Z., Feng, X. Y., Ma, Q. Y., Li, N. N., Jin, C. C., Hiroto, Y.*, Tan J. J.*
Org. Lett. 2023, 25, 7192. DOI: 10.1021/acs.orglett.3c02785
47)“Sulfonium-based precise alkyl transposition reactions”
Chen, J., Liu, S. L., Su, S. S., Fan, R., Zhang, R. R., Wei, M.*, Tan J. J.*
Sci. Adv. 2023, 9, eadi1370.(IF = 13.6)10.1126/sciadv.adi1370
46)“When Aryne Chemistry Meets Organosulfur Compounds”
Feng, X. Y., Fan, R., Zhuang, Z., Guo, Y. F., Tan J. J.*
Synlett. 2023. 10.1055/s-0042-1751476.
45)“Empowering boronic acids as hydroxyl synthons for aryne induced three-component coupling reactions”
Fan, R., Liu, S. H., Yan, Q., Wei, Y., Wang, J. W., Lan, Y.*, Tan J. J.*
Chem. Sci. 2023, 14, 4278.(IF = 9.969)10.1039/d3sc00072a
2022:
44)“Stereospecific synthesis of monofluoroalkenes and their deuterated analogues via Ag-catalyzed decarboxylation”
Liu X. Y., Shi F. X., Jin C. C., Liu B. B., Lei M.*, Tan J. J.*
J. Catal. 2022, 413, 1089.(IF = 8.047)https://doi.org/10.1016/j.jcat.2022.08.008
43) “Interfacial Composition of Surfactant Aggregates in the Presence of Fragrance: A Chemical Trapping Study”
Gong J. N., Yao K. X., Sun Q. H., Sun Y. J., Sun L. J., Liu C. Y.*, Xu B.*, Tan J. J., Zhao L., Xu. B. C.
Molecules 2022, 27, 4333.(IF = 4.927)10.3390/molecules27144333
42)“Photochemical/Electrochemical Degradation of Lignin β-O-4 Units: Applications of Ether Bond Cleavage Strategy”
Guo Y. F., Zhang. Y.*, Tan J. J.*
Chin. J. Chem. Edu. 2022, 43, 10.10.13884/j.1003-3807hxjy.2021030234
41) “Dehydroalanine Modification Sees the Light: A Photochemical Conjugate Addition Strategy”
Peng, X., Xu, K., Zhang, Q., Liu, L., Tan, J. J.*
Trends Chem. 2022. 4, 643.(IF = 22.448)10.1016/j.trechm.2022.04.008
40) “Recent Advances in Construction of C(sp2)-O Bonds via Aryne Participated Multicomponent Coupling Reactions”
Zhang, R. R., Peng, X., Tan, J. J.*
Synthesis 2022. 54, 5064. 10.1055/a-1748-7448
39)“Advances in C1-Deuterated Aldehyde Synthesis”
Guo, Y. F., Zhuang, Z., Liu, Y. G., Yang, X., Tan, C., Zhao, X. W., Tan, J. J.*
Coord. Chem. Rev. 2022, 463, 214525.(IF = 24.833)https://doi.org/10.1016/j.ccr.2022.214525
2021:
38)“Access to Deuterated Unnatural α-Amino Acids and Peptides by Photochemical Acyl Radical Addition”
Liu, L., Deng, Z. K., Xu, K*, Jiang, P. X., Du, H. G.*, Tan, J. J.*
Org. Lett. 2021, 23, 5099.10.1021/acs.orglett.1c01448
37) “Cleavage and Reassembly of the C═O Bond of 2-Alkynylbenzaldehydes: A Metal-Free Access to Inden-1-ones”
Liu, T., Yao, T. L.*, Zhang, F., Ju, Y., and Tan, J. J.*
J. Org. Chem. 2021, 86, 9455.https://doi.org/10.1021/acs.joc.1c00780
36) “Visible-light-promoted photocatalyst-free alkylation and acylation of benzothiazoles”
Jiang, P. X., Liu, L., Tan, J. J.*, Du, H. G.*
Org. Biomol. Chem. 2021, 19, 4487.DOI https://doi.org/10.1039/D1OB00734C
35) “Hf(OTf)4-Catalyzed 1,6-Conjugate Addition of 2-Alkyl-azaarenes to para-Quinone Methides”
Liu, X. Y., Liu, B. B., Shi, Z., Tan, C., Fan, R.; Li, Z., and Tan, J. J.*
J. Org. Chem. 2021, 86, 3615.https://doi.org/10.1021/acs.joc.0c02982
34) “Recent Progress in Aryne Participated Dearomatization Reactions”
Yan, Q., Fan, R., Liu, B. B., Su, S. S., Wang, B., Yao, T. L.*, Tan, J. J.*
Chin. J. Org. Chem., 2021, 41, 455.10.6023/cjoc202009009
33) “Reactions of Organophosphorus Compounds with Arynes: Reactivity and Mechanism”
Chen, J., Fan, R., Liu, Z. J.*, Tan, J. J.*
Adv. Synth. Catal. 2021, 363, 657. https://doi.org/10.1002/adsc.202001237
2020:
32) “Copper-Catalyzed Oxidative Fragmentation of Alkynes with NFSI Provides Aryl Ketones”
Tang, L., Yang, F., Cheng, H., Tan, C., Jin, C. C., Chen, H. F., Huang, Y. F., Zhang, S. F., Song, W. H., Tan, J. J.*
Org. Lett. 2020, 22, 8618.https://doi.org/10.1021/acs.orglett.0c03201
31) “Direct Radical Alkylation and Acylation of 2H-indazoles Using Substituted Hantzsch Esters as Radical Reservoirs”
Liu, L., Jiang, P. X., Liu, Y. G., Du, H. G.*, Tan, J. J.*
Org. Chem. Front. 2020, 7, 2278.DOI https://doi.org/10.1039/D0QO00507J
30) “A leap forward in sulfonium salt and sulfur ylide chemistry”
Fan, R., Tan, C., Liu, Y. G., Wei, Y., Zhao, X. W., Liu, X. Y., Tan, J. J.*, Yoshida, H.*
Chin. Chem. Lett. 2021, 32, 299.https://doi.org/10.1016/j.cclet.2020.06.003
29) “Synthesis of 2-(Arylthio)indolenines via Chemoselective Arylation of Thio-Oxindoles with Arynes”
Saputra, A., Fan, R., Yao, T. L.*, Chen, J., Tan, J. J.*
Adv. Synth. Catal. 2020, 362, 2683. https://doi.org/10.1002/adsc.202000308
28) “Exploration of Potential COVID-19 Drugs as Study Cases in Heterocyclic Chemistry Teaching”
Fan, R., Wei, Y*, Tan, J. J.*
University Chemistry, 2020, 35, 44.10.3866/pku.dxhx202006042
27) “Stereoselective synthesis of trans-aziridines via intramolecular oxidative C(sp3–H amination of β-amino ketones”
Tan, C., Liu, Y. G., Liu, X. Y., Jia, H. X., Xu, K.*, Huang, S. H., Wang, J. W., Tan, J. J.*
Org. Chem. Front. 2020, 7, 780.https://doi.org/10.1039/C9QO01489F
26) “Practical Synthesis of Phosphinic Amides/Phosphoramidates via Catalytic Oxidative Coupling of Amines and P(O)-H Compounds”
Tan, C., Liu, X. Y., Jia, H. X., Zhao, X. W., Chen, J., Wang, Z. Y.*, Tan, J. J.*
Chem. Eur. J. 2020, 26, 881.https://doi.org/10.1002/chem.201904237
25) “Direct benzylic functionalization of pyridines: Palladium-catalyzed mono-α-arylation of α-(2-pyridinyl)acetates with heteroaryl halides”
Jin, C. C., Xu, K., Fan, X., Liu, C. Y., Tan, J. J.*
Chin. Chem. Lett. 2020, 31, 91.https://doi.org/10.1016/j.cclet.2019.06.028
2019:
24) “Electrochemical Synthesis of trans-2,3-Disubstituted Aziridines via Oxidative Dehydrogenative Intramolecular C(sp3)–H Amination”
Wang, H. Q., Shi, J. X., Tan, J. J.*, Xu, W. T., Zhang, S.*, Xu, K.*
Org. Lett. 2019, 21, 9430.https://doi.org/10.1021/acs.orglett.9b03641
23) “Electrochemical synthesis of selenocyanated imidazo[1,5-a]quinolines under metal catalyst- and chemical oxidant-free conditions”
Zhang, J. J., Wang, H. Q.*, Chen, Y. R., Xie, H. Q., Ding, C. H., Tan, J. J.*, Xu, K.*
Chin. Chem. Lett. 2019, 31, 1576.
22) “Electrochemical synthesis of selenocyanated imidazo[1,5-a]quinolines under metal catalyst- and chemical oxidant-free conditions”
Zhang, J. J., Wang, H. Q.*, Chen, Y. R., Xie, H. Q., Ding, C. H., Tan, J. J.*, Xu, K.*
Chin. Chem. Lett. 2019, 31, 1576.
21) “Green Synthesis, Characterization, and Properties of Acyl Lysine, Serine, Threonine, and Methionine Derived from Three Types of Natural Oils”
Wang, N., Yao, K. X., Wang, Y. Z., Ti, J. H., Tan, J. J., Liu, C. Y.*, Zhang, G. J., Wang, C., Xu, B. C.*
J. Surfact. Deterg. 2019, 23, 239.10.1002/jsde.12365
20) “Host–guest interaction enabled chiroptical photo-switching and enhanced circularly polarized luminescence”
Ji, L. K., He, Q. W., Niu, D., Tan, J. J., Ouyang, Z. H., Liu, M. H.
Chem. Commun. 2019, 55, 11747.https://doi.org/10.1039/C9CC06305F
19) “I2/TBHP-Mediated tandem cyclization and oxidation reaction: Facile access to 2-substituted thiazoles and benzothiazoles”
Liu, L., Tan, C., Fan, R., Wang, Z. H., Du, H. G.*, Xu, K.*, Tan, J. J.*
Org. Biomol. Chem. 2019, 17, 252.DOI https://doi.org/10.1039/C8OB02826E
2018:
18) “Recent advance in sulfur ylide and sulfonium salts chemistry”
Tan, J. J.*
Chinese Science Bulletin, 2018, 63, 3612.https://doi.org/10.1360/N972018-00837
17) “Aryne triggered dearomatization reaction of isoquinolines and quinolines with chloroform”
Tan, J. J.*, Liu, B. B., Su, S. S.
Org. Chem. Front. 2018, 5, 3093.https://doi.org/10.1039/C8QO00838H
16) “The role of ortho-dearomatization reaction in constructing spirocyclic scaffolds with an all-carbon ring junction”
Shi, L. L., Zhang, W. G., Chen, S., Lu, L. L., Fan, R., Tan, J. J.*, Zheng, C.*
Curr. Org. Synth. 2018, 15, 904.10.2174/1570179415666180720110051
15) “An aryne triggered ring-opening fluorination of cyclic thioethers with potassium fluoride”
Fan, R., Liu, B. B., Zheng, T.-Y., Xu, K.*, Tan, C., Zeng, T. L., Su, S. S., Tan, J. J.*
Chem. Commun. 2018, 54, 7081.https://doi.org/10.1039/C8CC03766C
14) “Electrosynthesis of Trisubstituted 2-Oxazolines via Dehydrogenative Cyclization of β-Amino Arylketones”
Wang, H. Q., Zhang, J. J., Tan, J. J.*, Xin, L. L., Li, Y. P., Zhang, S., Xu, K.*
Org. Lett. 2018, 20, 2505.https://doi.org/10.1021/acs.orglett.8b00165
13) “Diverse Ring Opening of Thietanes and Other Cyclic Sulfides: an Electrophilic Aryne Activation Approach”
Zheng, T.-Y., Tan, J. J.*, Fan, R., Su, S. S., Liu, B. B., Tan, C., Xu, K.*
Chem. Commun. 2018, 54, 1303.https://doi.org/10.1039/C7CC08553B
2017:
12) “Model for the Enantioselectivity of Asymmetric Intramolecular Alkylations by Bis-Quaternized Cinchona Alkaloid-Derived Catalysts”
He, C. Q., Simon, A., Lam, Y.-h., Brunskill, A. P. J., Yasuda, N., Tan, J. J., Hyde, A. M., Sherer, E. C., Houk, K. N.*
J. Org. Chem. 2017, 82, 8645.https://doi.org/10.1021/acs.joc.7b01577
11) “Aryne Triggered [2,3]-Sigmatropic Rearrangement of Allyl and Propargyl Thioethers”
Tan, J. J.*, Zheng, T.-Y., Xu, K.*, Liu, C.-Y.,
Org. Biomol. Chem. 2017, 15, 4946. DOI https://doi.org/10.1039/C7OB00914C
10) “TBHP-promoted Direct Oxidation Reaction of Benzylic Csp3-H Bond to Ketones.”
Tan, J. J.*, Zheng, T.-Y., Yu, Y.-Q., Xu, K.*
RSC. Adv. 2017, 7, 15176.DOI https://doi.org/10.1039/C7RA00352H
2016:
9) “KOtBu-Promoted Oxidation of (Hetero)benzylic Csp3–H to Ketones with Molecular Oxygen.”
Wang, H.-Q., Wang, Z., Huang, H.-C., Tan, J. J.*, Xu, K.*
Org. Lett. 2016, 18, 5680.https://doi.org/10.1021/acs.orglett.6b02914
Before BUCT:
8) “Contemporary Asymmetric Phase Transfer Catalysis: Large Scale Applications in Industry.”
Tan, J. J.*, Yasuda, N.
Org. Process Res. Dev. 2015, 19, 1731.https://doi.org/10.1021/acs.oprd.5b00304
7) “Cobalt-Catalyzed Decarboxylative Acetoxylation of Amino Acids and Arylacetic Acids.”
Xu, K.*, Wang, Z.-Q., Zhang, J.-J., Yu, L.-T., Tan, J. J.*
Org. Lett. 2015, 17, 4476.https://doi.org/10.1021/acs.orglett.5b02142
6) “Suzuki-Miyaura Cross-coupling Reactions of Unprotected Haloimidazoles.”
Tan, J. J.*, Chen, Y.-G.*, Li, H.-M., Yasuda, N.
J. Org. Chem. 2014, 79, 8871.https://doi.org/10.1021/jo501326r
5) “The Supersilyl Group as a Carboxylic Acid Protecting Group: Application to Highly Stereoselective Aldol and Mannich Reactions.”
Tan, J. J., Akakura, M., Yamamoto, H.*
Angew. Chem. Int. Ed. 2013, 52, 7198. (Highlighted in SYNFACTS, 2013)https://doi.org/10.1002/anie.201300102
4) “Catalytic Asymmetric Claisen Rearrangement of Enolphosphonates: Construction of Vicinal Tertiary and All-Carbon Quaternary Centers.”
Tan, J. J., Cheon, C.-H., Yamamoto, H.*
Angew. Chem. Int. Ed. 2012, 51, 8264. (Highlighted in SYNFACTS, 2012)https://doi.org/10.1002/anie.201203092
3) “A Facile Access to Pyrroles from Amino Acids via a aza-Wacker Cyclization.”
Zhang, Z.-H., Zhang, J.-T., Tan, J. J., Wang, Z.-Y.*
J. Org. Chem. 2008, 73, 5180.https://doi.org/10.1021/jo800433b
2) “A Novel Palladium-catalyzed Hydroalkoxylation of Alkenes with a Migration of Double Bond.”
Tan, J. J., Zhang, Z.-H., Wang, Z.-Y.*
Org. Biomol. Chem. 2008, 6, 1344.https://doi.org/10.1039/B800838H
1) “A Facile Synthesis of 2-Methylquinolines via Pd-catalyzed aza-Wacker Oxidative Cyclization.”
Zhang, Z.-H., Tan, J. J., Wang, Z.-Y.*
Org. Lett. 2008, 10, 173. (Highlighted in SYNFACTS, 2008)https://doi.org/10.1021/ol702153x