Year |
Citation |
Score |
2023 |
Wang X, Wu Z, Tu G, Zhao Y, Xiong X. An efficient Selectfluor-mediated condensation of indoles and anthranilates for the synthesis of indoloquinazolinones. Chemical Communications (Cambridge, England). PMID 37432127 DOI: 10.1039/d3cc02673f |
0.483 |
|
2022 |
Wang X, Chen Z, Liu Q, Lin W, Xiong X. Amine organocatalysts for highly -selective chlorination of anilines with sulfuryl chloride. Chemical Communications (Cambridge, England). PMID 36325927 DOI: 10.1039/d2cc05320a |
0.333 |
|
2021 |
Xiong X, Wong J, Yeung YY. Silver Salt-Mediated Allylation Reactions Using Allyl Bromides. The Journal of Organic Chemistry. PMID 33861601 DOI: 10.1021/acs.joc.1c00480 |
0.598 |
|
2020 |
Xiong X, Zheng T, Wang X, Tse YS, Yeung Y. Access to Chiral Bisphenol Ligands (BPOL) through Desymmetrizing Asymmetric Ortho-Selective Halogenation Chem. 6: 919-932. DOI: 10.1016/J.Chempr.2020.01.009 |
0.593 |
|
2018 |
Xiong X, Yeung Y. Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications Acs Catalysis. 8: 4033-4043. DOI: 10.1021/Acscatal.8B00327 |
0.604 |
|
2017 |
Xiong X, Tan F, Yeung YY. Zwitterionic-Salt-Catalyzed Site-Selective Monobromination of Arenes. Organic Letters. PMID 28782957 DOI: 10.1021/Acs.Orglett.7B01899 |
0.622 |
|
2017 |
Xiong X, Deng CL, Li Z, Peng XS, Wong HNC. Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties Org. Chem. Front.,. 4: 682. DOI: DOI: 10.1039/c6qo00662k |
0.391 |
|
2017 |
Xiong X, Deng C, Li Z, Peng X, Wong HNC. Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties Organic Chemistry Frontiers. 4: 682-687. DOI: 10.1039/C6Qo00662K |
0.537 |
|
2016 |
Xiong X, Yeung YY. Highly ortho-Selective Chlorination of Anilines Using a Secondary Ammonium Salt Organocatalyst. Angewandte Chemie (International Ed. in English). PMID 27900807 DOI: 10.1002/Anie.201607388 |
0.613 |
|
2015 |
Deng CL, Xiong XD, Chik DT, Cai Z, Peng XS, Wong HN. 6,7-Bismethoxy-2,11-dihydroxytetraphenylene Derived Macrocycles: Synthesis, Structures, and Complexation with Fullerenes. Chemistry, An Asian Journal. PMID 26211744 DOI: 10.1002/Asia.201500689 |
0.695 |
|
2015 |
Minaeva VA, Baryshnikov GV, Minaev BF, Karaush NN, Xiong XD, Li MD, Phillips DL, Wong HN. Structure and spectroscopic characterization of tetrathia- and tetraselena[8]circulenes as a new class of polyaromatic heterocycles. Spectrochimica Acta. Part a, Molecular and Biomolecular Spectroscopy. 151: 247-61. PMID 26142658 DOI: 10.1016/J.Saa.2015.06.020 |
0.591 |
|
2015 |
Xiong X, Deng CL, Minaev BF, Baryshnikov GV, Peng XS, Wong HN. Tetrathio and tetraseleno[8]circulenes: synthesis, structures, and properties. Chemistry, An Asian Journal. 10: 969-75. PMID 25319048 DOI: 10.1002/Asia.201403028 |
0.699 |
|
2015 |
Xiong X, Deng CL, Minaev BF, Baryshnikov GV, Peng XS, Wong HNC. Tetrathio and Tetraseleno[8]circulenes: Synthesis, Structures, and Properties Chem. Asian J.. 10: 969. DOI: DOI: 10.1002/asia.201403028 |
0.391 |
|
2015 |
Deng CL, Xiong X, Chik D, Cai Z, Peng XS, Wong HNC. 6,7-Bismethoxy-2,11-dihydroxytetraphenylene Derived Macrocycles: Synthesis, Structures, and Complexation with Fullerenes Chem. Asian J.. 10: 2342. DOI: DOI : 10.1002/asia.201500689 |
0.372 |
|
2014 |
Xiong XD, Deng CL, Peng XS, Miao Q, Wong HN. Heteroatom-bridged tetraphenylenes: synthesis, structures, and properties. Organic Letters. 16: 3252-5. PMID 24909846 DOI: 10.1021/Ol501267Z |
0.7 |
|
2014 |
Xiong X, Deng CL, Peng XS, Miao Q, Wong HNC. Heteroatom-Bridged Tetraphenylenes: Synthesis, Structures, and Properties Org. Lett.. 16: 3252. DOI: dx.doi.org/10.1021/ol501267z |
0.403 |
|
2012 |
Xiong X, Jiang Y, Ma D. Assembly of N,N-disubstituted hydrazines and 1-aryl-1H-indazoles via copper-catalyzed coupling reactions. Organic Letters. 14: 2552-5. PMID 22545771 DOI: 10.1021/Ol300847V |
0.575 |
|
2009 |
Xiong X, Chen WX, Kuang YY, Chen FE. A Novel and Practical Synthesis of 2- Amino-5-hydroxypropiophenone Organic Preparations and Procedures International. 41: 423. DOI: DOI: 10.1080/00304940903187615 |
0.491 |
|
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