Hao Lu

3 weeks ago | dx.doi.org | Meng-Meng Song |Jing Li |Hao Lu |Jia-Xin Wang

Oct 17, 2024 | dx.doi.org | Hao Lu |Xinyu Li |Zhiqing Wang |Peng Du

Oct 17, 2024 | pubs.acs.org | Hao Lu |Xinyu Li |Zhiqing Wang |Peng Du

May 2, 2024 | journals.plos.org | Xuelian He |Aifen Zhou |Hao Lu |Yong Chen

Loading metrics After the publication and correction of this article [1, 2], additional concerns were noted about Fig 2A, 2D and 2G. Specifically:In Fig 2A, the WT and SC (scrambled control) panels appear to report overlapping image data. The quantitative migration data for G19 are missing from the bar graph in Fig 2D. In Fig 2G, the growth curves were labelled incorrectly. These errors are corrected in the updated version of Fig 2 provided here.

Dec 15, 2023 | chemistry-europe.onlinelibrary.wiley.com | Lifen Peng |Jiayi Chen |Yi Chen |Hao Lu

Sulfur-containing 1,2,3-triazoles display bioactivities like antidepressant, antifungal activity, antitumor, etc. Numerous approaches have been established to form sulfur-containing 1,2,3-triazoles. 4-Sulfanyl- and 5- sulfanyl-1,2,3-triazoles were produced by metal-catalyzed azide-alkyne cycloaddition (AAC), etc. N-Sulfonyl-1,2,3-triazoles were generated via the reaction of acetylides with sulfonyl azides, CuAAC.