Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Shaoyu Li"'
Publikováno v:
Science China Chemistry. 65:1142-1148
Publikováno v:
Chemical Communications. 58:4392-4395
A photoredox catalytic system was developed to construct N-heterobiaryls via direct arylation from readily accessible substrates. While phenols act as both coupling partner and proton donor, regular arenes were also applicable with HFIP as a solvent.
Autor:
Limin Yang, Qian Lu, Yuan Cui, Yong-Bin Wang, Quan-Hao Wu, Bin Tan, Shao-Hua Xiang, Jian-Hui Mao, Jie Lv, Shaoyu Li
Publikováno v:
Nature Chemistry. 13:982-991
Over the past three decades, organocatalysis has emerged as a powerful catalysis platform and has gradually been incorporated into the routine synthetic toolbox to obtain chiral molecules. However, its application in the site- and enantioselective fu
Publikováno v:
Chinese Journal of Chemistry. 39:1787-1796
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
Nature Communications
Nature Communications
As an important platform molecule, atropisomeric QUINOL plays a crucial role in the development of chiral ligands and catalysts in asymmetric catalysis. However, efficient approaches towards QUINOL remain scarce, and the resulting high production cos
Publikováno v:
Chemical Reviews. 121:4805-4902
Atropisomerism is a stereochemical behavior portrayed by three-dimensional molecules that bear rotationally restricted σ bond. Akin to the well-represented point-chiral molecules, atropisomerically chiral compounds are finding increasing utilities i
Publikováno v:
Chemical Communications. 57:8512-8515
N-Phenylphenothiazine as an inexpensive, highly reductive and oxygen tolerant organophotocatalyst has exhibited potential in various challenging photochemical transformations. Here we report a general and straightforward method to access structurally
Publikováno v:
Chinese Journal of Chemistry. 38:1503-1514
Autor:
Shaoyu Li, Qian-Jin An, Shao-Hua Xiang, Katherine L. Bay, Bin Tan, Peiyuan Yu, Wei-Yi Ding, Ying Chen, K. N. Houk
Publikováno v:
Chem. 6:2046-2059
Summary Functionalization of arenes represents the most efficient approach for constructing a core backbone of important aryl compounds. Compared with the well-developed electrophilic aromatic substitution and transition-metal-catalyzed C–H activat
Publikováno v:
Journal of the American Chemical Society. 142:7322-7327
The first copper-catalyzed atroposelective Michael-type addition between azonaphthalenes and arylboronic acids for the construction of biaryl atropisomers was established using a novel BINOL-derived phosphoramidite as a chiral ligand. A broad range o