Shelf-stable electrophilic reagents for trifluoromethylthiolation X Shao, C Xu, L Lu, Q Shen Accounts of Chemical Research 48 (5), 1227-1236, 2015 | 411 | 2015 |
N‐Trifluoromethylthiosaccharin: An Easily Accessible, Shelf‐Stable, Broadly Applicable Trifluoromethylthiolating Reagent C Xu, B Ma, Q Shen Angewandte Chemie 126 (35), 9470-9474, 2014 | 320 | 2014 |
Palladium-catalyzed trifluoromethylthiolation of aryl C–H bonds C Xu, Q Shen Organic letters 16 (7), 2046-2049, 2014 | 221 | 2014 |
N-Trifluoromethylthio-dibenzenesulfonimide: A Shelf-Stable, Broadly Applicable Electrophilic Trifluoromethylthiolating Reagent P Zhang, M Li, XS Xue, C Xu, Q Zhao, Y Liu, H Wang, Y Guo, L Lu, ... The Journal of Organic Chemistry 81 (17), 7486-7509, 2016 | 193 | 2016 |
Structure–reactivity relationship of trifluoromethanesulfenates: discovery of an electrophilic trifluoromethylthiolating reagent X Shao, C Xu, L Lu, Q Shen The Journal of Organic Chemistry 80 (6), 3012-3021, 2015 | 154 | 2015 |
Copper-catalyzed trifluoromethylthiolation of aryl and vinyl boronic acids with a shelf-stable electrophilic trifluoromethylthiolating reagent K Kang, C Xu, Q Shen Organic Chemistry Frontiers 1 (3), 294-297, 2014 | 128 | 2014 |
Lewis acid mediated trifluoromethylthio lactonization/lactamization C Xu, Q Shen Organic Letters 17 (18), 4561-4563, 2015 | 86 | 2015 |
A multistage halogen bond catalyzed strain-release glycosylation unravels new hedgehog signaling inhibitors C Xu, CCJ Loh Journal of the American Chemical Society 141 (13), 5381-5391, 2019 | 75 | 2019 |
Stable iso‐osmabenzenes from a formal [3+ 3] cycloaddition reaction of metal vinylidene with alkynols Q Zhao, L Gong, C Xu, J Zhu, X He, H Xia Angewandte Chemie-International Edition 50 (6), 1354, 2011 | 60 | 2011 |
Molecular editing in natural product synthesis C Hui, Z Wang, S Wang, C Xu Organic Chemistry Frontiers 9 (5), 1451-1457, 2022 | 53 | 2022 |
A robust and tunable halogen bond organocatalyzed 2-deoxyglycosylation involving quantum tunneling C Xu, VUB Rao, J Weigen, CCJ Loh Nature communications 11 (1), 4911, 2020 | 49 | 2020 |
Recent advances in difluoromethylthiolation X Xiao, ZT Zheng, T Li, JL Zheng, T Tao, LM Chen, JY Gu, X Yao, JH Lin, ... Synthesis 52 (02), 197-207, 2020 | 45 | 2020 |
Harnessing noncovalent interaction of chalcogen bond in organocatalysis: From the catalyst point of view W Yan, M Zheng, C Xu, FE Chen Green Synthesis and Catalysis 2 (4), 329-336, 2021 | 39 | 2021 |
An ultra-low thiourea catalyzed strain-release glycosylation and a multicatalytic diversification strategy C Xu, CCJ Loh Nature Communications 9 (1), 4057, 2018 | 39 | 2018 |
Simple photo-induced trifluoromethylation of aromatic rings H Egami, Y Ito, T Ide, S Masuda, Y Hamashima Synthesis 50 (15), 2948-2953, 2018 | 34 | 2018 |
Copper-catalyzed radical bis (trifluoromethylation) of alkynes and 1, 3-enynes H Shen, H Xiao, L Zhu, C Li Synlett 31 (01), 41-44, 2020 | 33 | 2020 |
Nucleophilic Trifluoromethylthiolation of Alkyl Chlorides, Bromides and Tosylates C Xu, Q Chen, Q Shen Chinese Journal of Chemistry 34 (5), 495-504, 2016 | 28 | 2016 |
Recent progress on trifluoromethylthiolation of (hetero) aryl C–H bonds with electrophilic trifluoromethylthiolating reagents C Xu, S Wang, Q Shen ACS Sustainable Chemistry & Engineering 10 (21), 6889-6899, 2022 | 24 | 2022 |
Nucleophilic Trifluoromethylation Reactions Involving Copper (I) Species: From Organometallic Insights to Scope ÁL Mudarra, SM de Salinas, MH Pérez-Temprano Synthesis 51 (14), 2809-2820, 2019 | 21 | 2019 |
Preparation of trifluorostyrenes via palladium-catalyzed coupling of arylboronic acids with chloro-and bromotrifluoroethylene C Xu, S Chen, L Lu, Q Shen The Journal of Organic Chemistry 77 (22), 10314-10320, 2012 | 19 | 2012 |