Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yue-Yan Zhang"'
Autor:
Yan Chen, Chun Hou, Liu-xin Zhao, Qiu-chen Cai, Ying Zhang, Da-lun Li, Yao Tang, Hong-yu Liu, Yun-yi Liu, Yue-yan Zhang, Ya-kun Yang, Cheng-wei Gao, Qian Yao, Qi-shun Zhu, Chuan-hai Cao
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
The incidence and associated mortality of lung cancer in tin miners in Gejiu County and farmers in Xuanwei Country, Yunnan Province have been very high in the world. Current published literatures on the molecular mechanisms of lung cancer initiation
Externí odkaz:
https://doaj.org/article/657ae05c70de4888b9aa35be3544782a
Autor:
Qiu-Chen Cai, Da-Lun Li, Ying Zhang, Yun-Yi Liu, Pei Fang, Si-Qin Zheng, Yue-Yan Zhang, Ya-Kun Yang, Chun Hou, Cheng-Wei Gao, Qi-Shun Zhu, Chuan-Hai Cao
Publikováno v:
Oncology letters. 24(6)
In tumor research, the occurrence and origin of tumors are the fundamental problems. In the 1970s, the basic discussion of the developmental biology problem of tumors was proposed, and it was believed that tumorigenesis is closely related to developm
Autor:
Jia-Lu Jin, Nan Dong, Yue-Yan Zhang, Jin-Pei Cheng, Bin Wang, Xiao-Song Xue, Bo-Xuan Tan, Cong Liu, Xin Li
Publikováno v:
Org. Biomol. Chem.. 10:413-420
The current work reports an organocatalytic strategy for the asymmetric catalysis of chiral benzofuran-2(3H)-ones bearing 3-position all-carbon quaternary stereocenters. Accordingly, highly enantioselective Michael addition reactions of 3-substituted
Publikováno v:
The Journal of Organic Chemistry. 76:5838-5845
A highly diastereo- and enantioselective asymmetric allylic alkylation reaction with respect to prochiral 3-substituted benzofuran-2(3H)-ones and MBH carbonate by a chiral biscinchona alkaloid catalyst was investigated. The corresponding adducts, con
Autor:
Jia-Lu Jin, Nan Dong, Jin-Pei Cheng, Xin Li, Yue-Yan Zhang, Bo-Xuan Tan, Cong Liu, Xiao-Song Xue
Publikováno v:
ChemInform. 43
A bifunctional Cinchona alkaloid-based organocatalyst efficiently catalyzes the asymmetric Michael addition of 3-substituted benzofuranones (I) and (IV) with bis(phenylsulfonyl)ethylene (II).
Autor:
Xiao-Song Xue, Bin Wang, Jia-Lu Jin, Nan Dong, Xin Li, Bo-Xuan Tan, Cong Liu, Yue-Yan Zhang, Jin-Pei Cheng
Publikováno v:
ChemInform. 43
Michael reaction of a variety of 3-substituted benzofuranones with β-nitroolefins proceeds efficiently in the presence of a tertiary amine—thiourea organocatalyst to give benzofuranones bearing an all-carbon quaternary stereocenter at position 3.
Publikováno v:
ChemInform. 42
The alkaloid efficiently promotes the coupling of 3-substituted benzofuranones with carbonates giving 3,3-disubstituted benzofuranones with moderate to high diastereo- and enantioselectivity.
Publikováno v:
Journal of Organic Chemistry; 7/15/2011, Vol. 76 Issue 14, p5238-5845, 4p