Xiaodong Xiong, Ph.D
Affiliations: | 2019- | Pharmacy | Nanchang University |
Area:
halogenation, asymmetric synthesisWebsite:
https://www.x-mol.com/groups/xiong_xiaodong?lang=enGoogle:
"Xiaodong Xiong"Mean distance: (not calculated yet)
Parents
Sign in to add mentorFen-er Chen | grad student | 2006-2009 | |
Dawei Ma | grad student | 2009-2012 | |
Henry N. C. Wong | post-doc | 2013-2015 | |
Ying-yeung Yeung | post-doc | 2015-2019 |
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Publications
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Wang X, Wu Z, Tu G, et al. (2023) An efficient Selectfluor-mediated condensation of indoles and anthranilates for the synthesis of indoloquinazolinones. Chemical Communications (Cambridge, England) |
Wang X, Chen Z, Liu Q, et al. (2022) Amine organocatalysts for highly -selective chlorination of anilines with sulfuryl chloride. Chemical Communications (Cambridge, England) |
Xiong X, Wong J, Yeung YY. (2021) Silver Salt-Mediated Allylation Reactions Using Allyl Bromides. The Journal of Organic Chemistry |
Xiong X, Zheng T, Wang X, et al. (2020) Access to Chiral Bisphenol Ligands (BPOL) through Desymmetrizing Asymmetric Ortho-Selective Halogenation Chem. 6: 919-932 |
Xiong X, Yeung Y. (2018) Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications Acs Catalysis. 8: 4033-4043 |
Xiong X, Tan F, Yeung YY. (2017) Zwitterionic-Salt-Catalyzed Site-Selective Monobromination of Arenes. Organic Letters |
Xiong X, Deng CL, Li Z, et al. (2017) Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties Org. Chem. Front.,. 4: 682 |
Xiong X, Deng C, Li Z, et al. (2017) Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties Organic Chemistry Frontiers. 4: 682-687 |
Xiong X, Yeung YY. (2016) Highly ortho-Selective Chlorination of Anilines Using a Secondary Ammonium Salt Organocatalyst. Angewandte Chemie (International Ed. in English) |
Deng CL, Xiong XD, Chik DT, et al. (2015) 6,7-Bismethoxy-2,11-dihydroxytetraphenylene Derived Macrocycles: Synthesis, Structures, and Complexation with Fullerenes. Chemistry, An Asian Journal |