Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Qiao-Ying Sun"'
Autor:
Li-Wen Xu, Ke-Fang Yang, Zheng Xu, Zhao Li, Zhan-Jiang Zheng, Qiao-Ying Sun, Jian Cao, Yu-Ming Cui
Publikováno v:
Chemical Communications. 55:6229-6232
The first example of palladium-catalyzed chelation-assisted C–H olefination of 2-amino biaryls using readily available vinylsilanes as unactivated olefinating reagents has been developed, affording valuable arylated vinylsilane compounds in moderat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f956886d407a0712fea9054a653a9cb
https://doi.org/10.1039/c9cc02199j
https://doi.org/10.1039/c9cc02199j
Publikováno v:
Synlett. 28:1432-1436
A palladium-catalyzed intramolecular direct arylation reaction of o-bromoaryl phosphine oxides was developed to afford a variety of P-stereogenic phosphole oxides in good yields. The enantioselectivities were closely associated with the specific stru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10afa49aa2e3b9868be14248e3c5bf9f
https://doi.org/10.1055/s-0036-1588983
https://doi.org/10.1055/s-0036-1588983
Autor:
Qiao-Ying, Sun, Zhao, Li, Zheng, Xu, Zhan-Jiang, Zheng, Jian, Cao, Ke-Fang, Yang, Yu-Ming, Cui, Li-Wen, Xu
Publikováno v:
Chemical communications (Cambridge, England). 55(44)
The first example of palladium-catalyzed chelation-assisted C-H olefination of 2-amino biaryls using readily available vinylsilanes as unactivated olefinating reagents has been developed, affording valuable arylated vinylsilane compounds in moderate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f46c95a2a07f2093b275f418eba8bf1
https://pubmed.ncbi.nlm.nih.gov/31086887
https://pubmed.ncbi.nlm.nih.gov/31086887
Autor:
Zheng Xu, Ke-Fang Yang, Zhan-Jiang Zheng, Qiao-Ying Sun, Jian Cao, Li-Wen Xu, Wei-Yang Ma, Yu-Ming Cui
Publikováno v:
Chemical communications (Cambridge, England). 54(76)
A palladium-catalyzed ketoxime-chelation-assisted enantioselective C–H olefination of 2-arylcyclohex-2-enone oxime ether with a wide range of olefins as coupling partners was developed. Employing ketoxime ether as an efficient directing group, a va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a825228bfe4cbb7ec6e71c1201b766a
https://pubmed.ncbi.nlm.nih.gov/30182108
https://pubmed.ncbi.nlm.nih.gov/30182108
Publikováno v:
Synlett; 2017, Vol. 28 Issue 12, p1432-1436, 5p