Copper-Catalyzed Asymmetric Hydroboration of 2H-Chromenes Using a Chiral Diphosphine Ligand

2019 ◽  
Vol 84 (13) ◽  
pp. 8638-8645 ◽  
Author(s):  
Xiufen Li ◽  
Chaoqiong Wang ◽  
Jianqiao Song ◽  
Zhihong Yang ◽  
Guofu Zi ◽  
...  
Synlett ◽  
2020 ◽  
Author(s):  
Shi-Liang Shi ◽  
Yuan Cai

AbstractAsymmetric hydroboration of simple and unactivated terminal alkenes (α-olefins), feedstock chemicals derived from the petrochemical industry, has not been efficiently realized for past decades. Using a bulky ANIPE ligand, we achieved a rare example of highly enantioselective copper-catalyzed Markovnikov hydroboration of α-olefins. The chiral secondary alkylboronic ester products were obtained in moderate to good yields and regioselectivities with excellent enantioselectivities.1 Introduction2 Conditions Optimization3 Substrate Scope4 Application5 Mechanistic Discussion6 Conclusions and Future Directions


iScience ◽  
2018 ◽  
Vol 10 ◽  
pp. 11-22 ◽  
Author(s):  
Can Liu ◽  
Xianjin Zhu ◽  
Pengxiang Zhang ◽  
Haijun Yang ◽  
Changjin Zhu ◽  
...  

ChemInform ◽  
2004 ◽  
Vol 35 (26) ◽  
Author(s):  
Anna M. Segarra ◽  
Carmen Claver ◽  
Elena Fernandez

ChemInform ◽  
2015 ◽  
Vol 46 (31) ◽  
pp. no-no
Author(s):  
Jun Guo ◽  
Jianhui Chen ◽  
Zhan Lu

Sign in / Sign up

Export Citation Format

Share Document