Zobrazeno 1 - 10
of 124
pro vyhledávání: '"Hao‐Yue Xiang"'
Publikováno v:
Journal of Organic Chemistry; 8/2/2024, Vol. 89 Issue 15, p10987-10997, 11p
Autor:
Chu-Ping Yuan, Yu Zheng, Zhen-Zhen Xie, Ke-Yi Deng, Hong-Bin Chen, Hao-Yue Xiang, Kai Chen, Hua Yang
Publikováno v:
Organic Letters. 25:1782-1786
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a06f10a38516e739e83fceee7531a84a
https://doi.org/10.1021/acs.orglett.3c00559
https://doi.org/10.1021/acs.orglett.3c00559
Autor:
Yi-Xuan Chen, Jun-Tao He, Mei-Chun Wu, Zhi-Lin Liu, Peng-Ju Xia, Kai Chen, Hao-Yue Xiang, Hua Yang
Publikováno v:
Chemical Communications. 59:6588-6591
A novel photo-induced strategy for oxidation of organosilanes to access silanols, promoted by a photoactive charge-transfer complex (CTC) between sodium benzenesulfinate and molecular O2, has been developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efdf515b5588e69aa7f174489444add1
https://doi.org/10.1039/d3cc01972a
https://doi.org/10.1039/d3cc01972a
Autor:
Jie Gao, Zhi-Peng Ye, Yu-Fei Liu, Xian-Chen He, Jian-Ping Guan, Fang Liu, Kai Chen, Hao-Yue Xiang, Xiao-Qing Chen, Hua Yang
Publikováno v:
Organic Letters. 24:4640-4644
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a15fd43abdcf0ff47111382a87109b17
https://doi.org/10.1021/acs.orglett.2c01750
https://doi.org/10.1021/acs.orglett.2c01750
Photocatalyzed Defluorinative Dichloromethylation of α-CF3 Alkenes Using CHCl3 as the Radical Source
Autor:
Mei-Chun Wu, Yi-Xuan Chen, Ming-Zhi Li, Jun-An Xiao, Zhi-Peng Ye, Jian-Ping Guan, Hao-Yue Xiang, Kai Chen, Hua Yang
Publikováno v:
The Journal of Organic Chemistry. 88:6354-6363
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1984fc03d609e719e249422bbdfe0f67
https://doi.org/10.1021/acs.joc.2c01106
https://doi.org/10.1021/acs.joc.2c01106
Autor:
Xian-Chen He, Ke-Rong Li, Jie Gao, Jian-Ping Guan, Hong-Bin Chen, Hao-Yue Xiang, Kai Chen, Hua Yang
Publikováno v:
Organic Letters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccd4cde42e5ff2bbd8d7cff4f469a992
https://doi.org/10.1021/acs.orglett.3c01219
https://doi.org/10.1021/acs.orglett.3c01219
Autor:
Zhi-Lin Liu, Zhi-Peng Ye, Yi-Xuan Chen, Yu Zheng, Zhen-Zhen Xie, Jian-Ping Guan, Jun-An Xiao, Kai Chen, Hao-Yue Xiang, Hua Yang
Publikováno v:
Organic Letters. 24:924-928
A highly modular 1,4-difunctionalization of 1,3-dienes with bromodifluoroacetamides and sulfinates/amines through a photoinduced palladium-catalyzed radical relay process is described herein. This developed protocol offers a facile and general route
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce848471b984dde9235efba5b591bced
https://doi.org/10.1021/acs.orglett.1c04293
https://doi.org/10.1021/acs.orglett.1c04293
Autor:
Zhi-Wei Wang, Yu Zheng, Yu-En Qian, Jian-Ping Guan, Wei-Dong Lu, Chu-Ping Yuan, Jun-An Xiao, Kai Chen, Hao-Yue Xiang, Hua Yang
Publikováno v:
The Journal of Organic Chemistry. 87:1477-1484
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b22ce4237b9609a98d966c813c43801
https://doi.org/10.1021/acs.joc.1c02796
https://doi.org/10.1021/acs.joc.1c02796
Autor:
Yu Zheng, Zhi-Wei Wang, Wen-Shuo Cheng, Zhen-Zhen Xie, Xian-Chen He, Yan-Shan Chen, Kai Chen, Hao-Yue Xiang, Xiao-Qing Chen, Hua Yang
Publikováno v:
The Journal of Organic Chemistry. 87:974-984
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b149279aa3f48fd60fec7c0802ef2ff
https://doi.org/10.1021/acs.joc.1c02149
https://doi.org/10.1021/acs.joc.1c02149
Publikováno v:
Chemical Communications. 58:11591-11594
A photoredox-catalysed chlorination of quinoxalin-2(1H)-ones was developed by using CHCl3 as a chlorine source, thus affording various 3-chloroquinoxalin-2(1H)-ones in moderate to high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::759b5a23bbcd2731b6c88910994cd940
https://doi.org/10.1039/d2cc04520f
https://doi.org/10.1039/d2cc04520f