Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Quannan Wang"'
Publikováno v:
Green Synthesis and Catalysis, Vol 4, Iss 3, Pp 206-225 (2023)
Transition-metal-catalyzed C–H bond functionalization has attracted tremendous attention as an increasingly important protocol for the construction of C–C and C–X bonds. In particular, C–H bond functionalization assisted by the phosphorus-con
Externí odkaz:
https://doaj.org/article/cfb5f33a1dc0413fa4db18e07a995019
Autor:
Chen-Xu Liu, Pei-Pei Xie, Fangnuo Zhao, Quannan Wang, Zuolijun Feng, Haoyang Wang, Chao Zheng, Shu-Li You
Publikováno v:
Journal of the American Chemical Society. 145:4765-4773
Publikováno v:
Organic Chemistry Frontiers. 10:1537-1543
A novel approach to synthesize β,β-diaryl substituted α,β-unsaturated esters in high efficiency and with excellent regio- and stereoselectivities was developed.
Publikováno v:
Organic Chemistry Frontiers. 10:1680-1685
An efficient approach for the exclusively regioselective construction of 1,5-di/ox-azonanes via Pd-catalyzed [5 + 4] cycloaddition has been developed.
Autor:
Quannan WANG1,2 quannanwang@yeah.net
Publikováno v:
Thermal Science. 2022, Vol. 26 Issue 3A, p2361-2372. 12p.
Publikováno v:
Nature Synthesis. 2:49-57
Autor:
Quannan Wang, Yu-Han Nie, Chen-Xu Liu, Wen-Wen Zhang, Zhi-Jie Wu, Qing Gu, Chao Zheng, Shu-Li You
Publikováno v:
ACS Catalysis. 12:3083-3093
Autor:
Fangnuo Zhao, Zuolijun Feng, Chen-Xu Liu, Quannan Wang, Su-Zhen Zhang, Shu-Li You, Wen-Wen Zhang, Pusu Yang, Qing Gu
Publikováno v:
Chem Catalysis. 2:102-113
Summary Oxidative C-H/C-H cross-coupling reactions between two (hetero)arenes through 2-fold C-H activation offer rapid assembly of diverse bi(hetero)aryls. Herein, a Pd-catalyzed asymmetric oxidative C-H/C-H cross-coupling reaction of ferrocenes wit
Publikováno v:
Science Bulletin. 66:210-213
Publikováno v:
Reference Module in Chemistry, Molecular Sciences and Chemical Engineering
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a1c3a87c35bb0330ff3f55d5d10a26a
https://doi.org/10.1016/b978-0-12-820206-7.00087-1
https://doi.org/10.1016/b978-0-12-820206-7.00087-1