Chiral Phosphoric Acid Catalyzed Asymmetric Synthesis of Axially Chiral Compounds

Author(s):  
Bing‐Chao Da ◽  
Shao‐Hua Xiang ◽  
Shaoyu Li ◽  
Bin Tan
2021 ◽  
Vol 17 ◽  
pp. 2729-2764
Author(s):  
Alemayehu Gashaw Woldegiorgis ◽  
Xufeng Lin

In recent years, the synthesis of axially chiral compounds has received considerable attention due to their extensive application as biologically active compounds in medicinal chemistry and as chiral ligands in asymmetric catalysis. Chiral phosphoric acids are recognized as efficient organocatalysts for a variety of enantioselective transformations. In this review, we summarize the recent development of chiral phosphoric acid-catalyzed synthesis of a wide range of axially chiral biaryls, heterobiaryls, vinylarenes, N-arylamines, spiranes, and allenes with high efficiency and excellent stereoselectivity.


Heterocycles ◽  
2019 ◽  
Vol 99 (2) ◽  
pp. 1398
Author(s):  
Takaaki Sumiyoshi ◽  
Kyoji Ishida ◽  
Masahiro Shimizu ◽  
Yu-suke Yamai ◽  
Itaru Natsutani ◽  
...  

2020 ◽  
Vol 7 (16) ◽  
pp. 2255-2262 ◽  
Author(s):  
You-Dong Shao ◽  
Dan-Dan Han ◽  
Wen-Yue Ma ◽  
Dao-Juan Cheng

A chiral phosphoric acid catalyzed atroposelective annulation between 2-aminoaryl ketones and alicyclic ketones has been developed to access a new library of enantioenriched axially chiral 9-aryltetrahydroacridines.


2019 ◽  
Vol 55 (84) ◽  
pp. 12715-12718 ◽  
Author(s):  
Huijun Yuan ◽  
Yao Li ◽  
Hanhui Zhao ◽  
Zhihong Yang ◽  
Xin Li ◽  
...  

The first catalytic asymmetric reaction of azonaphthalene with pyrazolone has been established. A wide range of axially chiral pyrazole derivatives have been achieved in good yields (68–99%) with excellent enantioselectivities (83–98% ee) by utilizing chiral phosphoric acid as a catalyst.


2019 ◽  
Vol 60 (18) ◽  
pp. 1262-1264 ◽  
Author(s):  
Amber M. Kelley ◽  
Eni Minerali ◽  
Jennifer E. Wilent ◽  
Nicholas J. Chambers ◽  
Kyla J. Stingley ◽  
...  

2017 ◽  
Vol 4 (7) ◽  
pp. 1407-1410 ◽  
Author(s):  
En Xie ◽  
Abdul Rahman ◽  
Xufeng Lin

An enantioselective aza-Friedel–Crafts reaction of indoles with 1-trifluoromethyl-3,4-dihydro-β-carbolines has been developed to afford tetrahydro-β-carbolines with a CF3- and indole-containing quaternary stereocenter by using chiral phosphoric acid catalysis.


2018 ◽  
Vol 57 (34) ◽  
pp. 11004-11008 ◽  
Author(s):  
Caizhen Yue ◽  
Fei Na ◽  
Xiantao Fang ◽  
Yang Cao ◽  
Jon C. Antilla

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