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Organic Letters|June 14, 2024
Electrochemical Enaminone-Thioamide Annulation and Thioamide Dimeric Annulation for the Tunable Synthesis of Thiazoles and 1,2,4-ThiadiazoleQihui Huang, Jianchao Liu, Jie-Ping Wan
The Journal of Organic Chemistry|January 17, 2019
Visible Light-Induced Thiocyanation of Enaminone C-H Bond to Access Polyfunctionalized Alkenes and Thiocyano ChromonesYong Gao, Yunyun Liu, Jie-Ping Wan
The Journal of Organic Chemistry|March 3, 2018
Copper-Catalyzed One-Pot N-Acylation and C5-H Halogenation of 8-Aminoquinolines: The Dual Role of Acyl HalidesYi Dua, Yunyun Liu, Jie-Ping Wan
Chemical Communications (Cambridge, England)|June 20, 2018
Redox neutral [4+2] benzannulation of dienals and tertiary enaminones for benzaldehyde synthesisLu Yang, Li Wei, Jie-Ping Wan
Organic & Biomolecular Chemistry|March 9, 2022
Recent advances in transition metal-free annulation toward heterocycle diversity based on the C-N bond cleavage of enaminone platformXiao Yun Chen, Xiaotong Zhang, Jie-Ping Wan
Chemical Communications (Cambridge, England)|June 28, 2024
Visible-light-induced Ritter-type amidation of α-hydroxy ketones in the selective synthesis of α,α-diamido and monoamido ketonesEnrong Tang, Quan-Quan Zhou, Jie-Ping Wan
The Journal of Organic Chemistry|July 9, 2014
Diastereoselective construction of tetrahydropyridine fused bicyclic structures via three-component domino reactionJie-Ping Wan, Yunfang Lin, Qing Huang, et al.
Beilstein Journal of Organic Chemistry|October 25, 2017
Transition-metal-free synthesis of 3-sulfenylated chromones via KIO3-catalyzed radical C(sp2)-H sulfenylationYanhui Guo, Shanshan Zhong, Li Wei, et al.
The Journal of Organic Chemistry|December 20, 2018
Synthesis of α-Keto Thioamides by Metal-Free C═C Bond Cleavage in Enaminones Using Elemental SulfurLu Gan, Yong Gao, Li Wei, et al.
Beilstein Journal of Organic Chemistry|June 25, 2016
Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp(3))-H arylationYunyun Liu, Yi Zhang, Xiaoji Cao, et al.
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