Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Li-li Liao"'
Autor:
Jie Liu, Wei Wang, Li-Li Liao, Wei Zhang, Jun-Ping Yue, Yi Liu, Xiao-Wang Chen, Jian-Heng Ye, Da-Gang Yu
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-9 (2024)
Abstract Aryl thiols have proven to be a useful class of electron donors and hydrogen atom sources in photochemical processes. However, the direct activation and functionalization of C(sp2)–S bonds in aryl thiols remains elusive in the field of pho
Externí odkaz:
https://doaj.org/article/94939a80cde14ae48a24338c1d4244c1
Autor:
Yue Liu, Xiao-ya Zhu, Li-li Liao, Zhan-hui Zhang, Tao-sheng Huang, Ling Zhang, Xi-wen Jiang, Yi Ma
Publikováno v:
Biology Direct, Vol 19, Iss 1, Pp 1-15 (2024)
Abstract Background Most patients with acute myeloid leukemia (AML) eventually develop drug resistance, leading to a poor prognosis. Dysregulated long gene non coding RNAs (lincRNAs) have been implicated in chemoresistance in AML. Unfortunately, the
Externí odkaz:
https://doaj.org/article/7e415f1e88de446e99462b39ab2b8281
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-10 (2023)
Abstract Photocatalytic carboxylation of alkenes with CO2 is a promising and sustainable strategy to synthesize high value-added carboxylic acids. However, it is challenging and rarely investigated for unactivated alkenes due to their low reactivitie
Externí odkaz:
https://doaj.org/article/7342db3cd57d4148aae36aaf4a6bda48
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Electrochemistry is a promising approach to make existing chemical protocols milder, but many simple transformations of feedstocks are still out of reach. Here, the authors transform unactivated aryl and alkyl (pseudo)halides into carboxylic acids, v
Externí odkaz:
https://doaj.org/article/9aca5eb4e50b4d3eb207e93c2f895a21
Autor:
Guang-Mei Cao, Xin-Long Hu, Li-Li Liao, Si-Shun Yan, Lei Song, Jason J. Chruma, Li Gong, Da-Gang Yu
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Compounds bearing a carbonyl group, such as aldehydes and ketones, are important industrial chemicals and widespread in pharmaceuticals and natural products. Here, the authors report a strategy for visible-light photoredox-catalyzed umpolung carboxyl
Externí odkaz:
https://doaj.org/article/9b7f948cac0f47a2b8b39d2e4feae65e
Autor:
Wen-Jun Zhou, Zhe-Hao Wang, Li-Li Liao, Yuan-Xu Jiang, Ke-Gong Cao, Tao Ju, Yiwen Li, Guang-Mei Cao, Da-Gang Yu
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Catalytic reductive coupling of two electrophiles and one C = C bond is usually performed by two electron transfer metal catalysis. Herein, the authors show a visible light photoredox-catalyzed successive single electron transfer leading to dearomati
Externí odkaz:
https://doaj.org/article/526c62d20baf485497257679efc84290
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
Phosphonyl and carboxyl groups are valuable functional groups, however their simultaneous incorporation via catalytic difunctionalization of alkenes has not been realized yet. Here the authors report the phosphonocarboxylation of alkenes with CO2 via
Externí odkaz:
https://doaj.org/article/75e6e53c912b4d1dac7a1c83c2c6ee58
Autor:
Li-Li Liao, 廖梨里
101
In the environment that the rate of using the mobile phone is almost reaching the peak, the progress of mobile phone technology changes the needs of mobile phone market and it also shows the importance of the youngster’s mobile phone usage
In the environment that the rate of using the mobile phone is almost reaching the peak, the progress of mobile phone technology changes the needs of mobile phone market and it also shows the importance of the youngster’s mobile phone usage
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/vq2f77
Autor:
Meng Miao, Lei Zhu, Hong Zhao, Lei Song, Si-Shun Yan, Li-Li Liao, Jian-Heng Ye, Yu Lan, Da-Gang Yu
Publikováno v:
Science China Chemistry. 66:1457-1466
Autor:
Wei Zhang, Li‐Li Liao, Li Li, Yi Liu, Long‐Fei Dai, Guo‐Quan Sun, Chuan‐Kun Ran, Jian‐Heng Ye, Yu Lan, Da‐Gang Yu
Publikováno v:
Angewandte Chemie International Edition. 62