Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yu‐Yong Luan"'
Synthesis of C ‐Aryl Glycosides via Ru‐Catalyzed Remote C−H Glycosylation of 8‐Aminoquinoline Amides
Autor:
Wei‐Yu Shi, Hu‐Yi Li, Xue‐Ya Gou, Yu‐Yong Luan, Nian Zheng, Zhi‐Jie Niu, Zhe Zhang, Xue‐Yuan Liu, Yong‐Min Liang
Publikováno v:
Advanced Synthesis & Catalysis. 364:2796-2800
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2978cde55c93eb138cae6ca78d46e2c2
https://doi.org/10.1002/adsc.202200549
https://doi.org/10.1002/adsc.202200549
Publikováno v:
Organic Letters. 24:1136-1140
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c83f67ca373fc3b636bcf0f29a4b2e80
https://doi.org/10.1021/acs.orglett.1c04182
https://doi.org/10.1021/acs.orglett.1c04182
Autor:
Xue‐Ya Gou, Yuke Li, Wei‐Yu Shi, Yu‐Yong Luan, Ya‐Nan Ding, Yang An, Yan‐Chong Huang, Bo‐Sheng Zhang, Xue‐Yuan Liu, Yong‐Min Liang
Publikováno v:
Angewandte Chemie International Edition. 61
C-aryl glycosides are popular basic skeletons in biochemistry and pharmaceutical chemistry. Herein, ruthenium-catalyzed highly stereo- and site-selective ortho- and meta-C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7077660b605b8ed176e0b8eee4e4b23
https://doi.org/10.1002/anie.202205656
https://doi.org/10.1002/anie.202205656
Autor:
Yong-Min Liang, Yu-Yong Luan, Bo-Sheng Zhang, Wei-Yu Shi, Yang An, Xue-Ya Gou, Cui-Tian Wang, Yuke Li
Publikováno v:
ACS Catalysis. 11:4263-4270
Free radical cyclization has emerged as one of the most important reaction types, which is widely used in natural product synthesis, pharmaceutical chemistry, and materials science. This report des...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5af54d9423d78c3def50ffca1e6994d8
https://doi.org/10.1021/acscatal.1c00359
https://doi.org/10.1021/acscatal.1c00359
Autor:
Ya-Nan Ding, Wei-Yu Shi, Zhi-Jie Niu, Xue-Ya Gou, Yu-Yong Luan, Zhe Zhang, Xi Chen, Yong-Min Liang, Nian Zheng
Publikováno v:
Chemical Communications. 57:8945-8948
C-Aryl glycosides are of high value as drug candidates. Here a novel and cost-effective nickel catalyzed ortho-CAr–H glycosylation reaction with high regioselectivity and excellent α-selectivity is described. This method shows great functional gro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b021a0e653403ceb11aff1e9851d30ba
https://doi.org/10.1039/d1cc03589d
https://doi.org/10.1039/d1cc03589d
Autor:
Wei-Yu, Shi, Ya-Nan, Ding, Nian, Zheng, Xue-Ya, Gou, Zhe, Zhang, Xi, Chen, Yu-Yong, Luan, Zhi-Jie, Niu, Yong-Min, Liang
Publikováno v:
Chemical communications (Cambridge, England).
C-Aryl glycosides are of high value as drug candidates. Here a novel and cost-effective nickel catalyzed ortho-CAr-H glycosylation reaction with high regioselectivity and excellent α-selectivity is described. This method shows great functional group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3060d0e7d65cf3d29366b6544cc7ee62
https://pubmed.ncbi.nlm.nih.gov/34397048
https://pubmed.ncbi.nlm.nih.gov/34397048