Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Zhi-Chao Cao"'
Autor:
Zishuo Zhang, Jintong Zhang, Quan Gao, Yu Zhou, Mingyu Yang, Haiqun Cao, Tingting Sun, Gen Luo, Zhi-Chao Cao
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-10 (2022)
Transition-metal catalyzed alkylative cross-couplings are established, powerful tools for the installation of alkyl groups. Here, the authors unlock a C(sp3)–C(sp2) cross-coupling via the asymmetric activation of the aromatic C–O bond by bis-liga
Externí odkaz:
https://doaj.org/article/cb7f42e18d6046488e61f7da5dfc1ad6
Autor:
Zhi-chao, Cao, Zhang, Lingling
Publikováno v:
In Journal of Visual Communication and Image Representation August 2019 63
Publikováno v:
ACS Catalysis. 13:3702-3709
Publikováno v:
ACS Catalysis. 13:2142-2148
Autor:
Zishuo Zhang, Jintong Zhang, Quan Gao, Yu Zhou, Mingyu Yang, Haiqun Cao, Tingting Sun, Gen Luo, Zhi-Chao Cao
Publikováno v:
Nature communications. 13(1)
Nonpolar alkyl moieties, especially methyl group, are frequently used to modify bioactive molecules during lead optimization in medicinal chemistry. Thus transition-metal catalyzed alkylative cross-coupling reactions by using readily available and en
Publikováno v:
Chinese Journal of Chemistry. 37:781-785
Publikováno v:
Nanoscience and Nanotechnology Letters. 11:56-60
Publikováno v:
Organic Letters. 20:1995-1998
The first successful catalytic borylation of unactivated aromatic C-N bonds of tertiary anilines without the preactivation or any directing groups is demonstrated. The reactivity of both N,N-dialkylarylamines and N-arylpyrroles were investigated syst
Autor:
Zhang-Jie Shi, Zhi-Chao Cao
Publikováno v:
Journal of the American Chemical Society. 139:6546-6549
In this article a successful protocol was developed to construct carbon–carbon bonds by the extrusion of the O atom of ethers via nickel catalysis in the presence of reductants. This methodology is featured as a highly economic route to construct s
Publikováno v:
Journal of the American Chemical Society; 11/10/2021, Vol. 143 Issue 44, p18380-18387, 8p