Zobrazeno 1 - 10
of 146
pro vyhledávání: '"Zhishan Su"'
Autor:
Shun Li, Juan Tang, Yonglin Shi, Meixin Yan, Yihua Fu, Zhishan Su, Jiaqi Xu, Weichao Xue, Xueli Zheng, Yicen Ge, Ruixiang Li, Hua Chen, Haiyan Fu
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-9 (2024)
Abstract Regioselective C–H functionalization of pyridines remains a persistent challenge due to their inherent electronically deficient properties. In this report, we present a strategy for the selective pyridine C3-H thiolation, selenylation, and
Externí odkaz:
https://doaj.org/article/ec0b7342a6a4496e942a30c8ee6acf50
Organocatalytic skeletal reorganization for enantioselective synthesis of S-stereogenic sulfinamides
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-10 (2024)
Abstract The enantioselective synthesis of S-stereogenic sulfinamides has garnered considerable attention due to their structural and physicochemical properties. However, catalytic asymmetric synthesis of sulfinamides still remains daunting challenge
Externí odkaz:
https://doaj.org/article/f057a24ec95c4a62a20ed62267363370
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-11 (2023)
Abstract The precise and efficient construction of axially chiral scaffolds, particularly toward the aryl-alkene atropoisomers with impeccably full enantiocontrol and highly structural diversity, remains greatly challenging. Herein, we disclose an or
Externí odkaz:
https://doaj.org/article/aabced401fd3401c8b9fc9d7e1b4f20c
Autor:
Tianbao Hu, Chen Zhao, Yan Zhang, Yuzhong Kuang, Lu Gao, Wanshu Wang, Zhishan Su, Zhenlei Song
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-9 (2023)
Abstract Organosilanes possessing an enantioenriched stereogenic silicon center are important in many branches of chemistry, yet they remain challenging to synthesize in a practical and scalable way. Here we report a dynamic kinetic silyletherificati
Externí odkaz:
https://doaj.org/article/35aa4ad9bb4a4ed69719162db60f7bff
Publikováno v:
Molecules, Vol 26, Iss 7, p 1965 (2021)
Density functional theory (DFT) calculations were performed to investigate the mechanism and the enantioselectivity of the aza-Henry reaction of isatin-derived ketimine catalyzed by chiral guanidine–amide catalysts at the M06-2X-D3/6-311+G(d,p)//M0
Externí odkaz:
https://doaj.org/article/7337d6926cb546e3be8e907cbd5ef074
Publikováno v:
Catalysts, Vol 10, Iss 9, p 1079 (2020)
The reaction mechanism and origin of asymmetric induction for conjugate addition of cyanide to the C=C bond of olefin were investigated at the B3LYP-D3(BJ)/6-31+G**//B3LYP-D3(BJ)/6-31G**(SMD, toluene) theoretical level. The release of HCN from the re
Externí odkaz:
https://doaj.org/article/08a9cbc987244119a72bf8dd9543f33a
Autor:
Hongkui Zhang, Jian-Ping Tan, Xiaoyu Ren, Fan Wang, Jia-Yan Zheng, Jiajia He, Yu Feng, Zhipeng Xu, Zhishan Su, Tianli Wang
Publikováno v:
Chemical Science; 8/14/2024, Vol. 15 Issue 30, p12017-12025, 9p
Publikováno v:
ACS Catalysis. 13:4656-4666
Autor:
Xufeng Nie, Mei Wang, Yihua Fu, Jiaqi Xu, Xueli Zheng, Hua Chen, Zhishan Su, Haiyan Fu, Ruixiang Li
Publikováno v:
Journal of Catalysis. 417:153-163
New chiral N-heterocyclic olefin bifunctional organocatalysis in α-functionalization of β-ketoesters
Publikováno v:
Science China Chemistry. 66:147-154