Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Can-Liang Ma"'
Autor:
Qi Zhang, Ning-Jing Song, Can-Liang Ma, Yun Zhao, Yong Li, Juan Li, Xiao-Ming Li, Qing-Qiang Kong, Cheng-Meng Chen
Publikováno v:
Molecules, Vol 28, Iss 8, p 3458 (2023)
Silicon–based composites are promising candidates as the next–generation anode materials for high–performance lithium–ion batteries (LIBs) due to their high theoretical specific capacity, abundant reserves, and reliable security. However, exp
Externí odkaz:
https://doaj.org/article/14b446de007d4f8192150d9b613fef6e
Autor:
Kai Guo, Xin Yuan, Can-Liang Ma, Xin-Peng Zhang, Qin Longzhou, Sun Qi, Duan Xiu, Shan-Shan Zhu, Jiang-Kai Qiu, Meng-Yu Wu, Jie Liu
Publikováno v:
Green Chemistry. 23:8916-8921
A photoinduced 1,4-heteroaryl migration from a carbon center to a nitrogen center accompanied by a cyanoalkylacylation of heterocyclic-substituted azidyl homoallylic alcohols and cycloketone oxime esters has been described. This simple and powerful p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d44e462062b5a622ce3393800a3121b9
https://doi.org/10.1039/d1gc03060d
https://doi.org/10.1039/d1gc03060d
Autor:
Xin-Yuan Liu, Fu-Li Wang, Qiang-Shuai Gu, Can-Liang Ma, Zhong-Liang Li, Sheng-Peng Jiang, Xiao-Yang Dong, Yu-Feng Zhang
Publikováno v:
Nature Chemistry. 11:1158-1166
Continued development of the Sonogashira coupling has made it a well established and versatile reaction for the straightforward formation of C-C bonds, forging the carbon skeletons of broadly useful functionalized molecules. However, asymmetric Sonog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b7447907ee29437e65dd212c5c642a1
https://doi.org/10.1038/s41557-019-0346-2
https://doi.org/10.1038/s41557-019-0346-2
Autor:
Xin-Yuan Liu, Yang Zeng, Guan-Yuan Jiao, Qiang-Shuai Gu, Jin-Shun Lin, Xiao-Yang Dong, Xian-Qi Guo, Fu-Li Wang, Can-Liang Ma
Publikováno v:
Chem. 3:979-990
Summary Catalytic asymmetric diamination of alkenes is a highly attractive method for creating chiral vicinal diamines, which are ubiquitous in biologically active molecules and versatile ligands as well as organocatalysts. We report the use of O -ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::244271ab5bc1493b5b7bcaeb84c1ea54
https://doi.org/10.1016/j.chempr.2017.10.008
https://doi.org/10.1016/j.chempr.2017.10.008
Autor:
Xiao-Yang, Dong, Yu-Feng, Zhang, Can-Liang, Ma, Qiang-Shuai, Gu, Fu-Li, Wang, Zhong-Liang, Li, Sheng-Peng, Jiang, Xin-Yuan, Liu
Publikováno v:
Nature chemistry. 11(12)
Continued development of the Sonogashira coupling has made it a well established and versatile reaction for the straightforward formation of C-C bonds, forging the carbon skeletons of broadly useful functionalized molecules. However, asymmetric Sonog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6135f3a37ffd5c32fe2718a65c152f00
https://pubmed.ncbi.nlm.nih.gov/31636393
https://pubmed.ncbi.nlm.nih.gov/31636393
Autor:
Xiaolong Zhu, Bin Tan, Xiao-Hua Li, Can-Liang Ma, Xiaowu Dong, Xin-Yuan Liu, Xiao-Long Yu, Yongzhou Hu
Publikováno v:
Organic Chemistry Frontiers. 3:324-329
The Au-catalyzed tandem process of aminoalkynes was explored, providing simple and efficient access to richly functionalized dipyrroloquinoline frameworks with good to excellent yields. The reaction exhibits great efficiency and high atom economy in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9bb1cdb725c64d9d519f16c80813dd3
https://doi.org/10.1039/c5qo00354g
https://doi.org/10.1039/c5qo00354g
Publikováno v:
Advanced Synthesis & Catalysis. 357:569-575
A convenient platinum-catalyzed tandem cyclization reaction from readily available aminoalkynes and enones has been developed to efficiently prepare multiply substituted indolines in good yields under microwave irradiation within a short reaction tim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cf5f81015d26c2ecdb66601e44a619a
https://doi.org/10.1002/adsc.201400933
https://doi.org/10.1002/adsc.201400933
Autor:
Xiaowu Dong, Yong Yang, Min-Kui Zhang, Jin-Hao Zhao, Rong Sheng, Chao Shen, Can-Liang Ma, Yongzhou Hu
Publikováno v:
Scientific Reports
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
A synthetic method for diversely substituted tetrahydropyrrolo[1,2-a]quinolines was developed via CuCl-catalyzed cascade transformation of internal aminoalkynes with alkynes under microwave- irradiation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ec9e4f5defff90802b66043ba1029d8
https://doi.org/10.1038/s41598-017-16887-0
https://doi.org/10.1038/s41598-017-16887-0
Autor:
Xiang-Yu Zhang, Xin-Yuan Liu, Ya-Ping Xiong, Lin Huang, Mingyue Wu, Li-Jiao Zhao, Bin Tan, Can-Liang Ma
Publikováno v:
Organic Letters. 16:1000-1003
A novel domino copper-catalyzed trifluoromethylated Meyer-Schuster rearrangement reaction with Togni's reagent was developed, leading to α-trifluormethyl (CF3) enone products with moderate to good yields. Furthermore, α-CF3 enones can be transforme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c6af8d9c8f3d3c88f478febecea526e
https://doi.org/10.1021/ol403741m
https://doi.org/10.1021/ol403741m
Publikováno v:
ChemInform. 46
The authors presume that the reaction proceeds via a tandem process involving intramolecular hydroamination of aminoalkynes, Michael addition of enones, aldol condensation, and intermolecular transfer hydrogenation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::741ee8e2ef7f74b1f804d35da4d1ebc7
https://doi.org/10.1002/chin.201526138
https://doi.org/10.1002/chin.201526138