Kinetic Resolution of Aziridines via Catalytic Asymmetric Ring-Opening Reaction with Mercaptobenzothiazoles

2019 ◽  
Vol 21 (15) ◽  
pp. 5928-5932 ◽  
Author(s):  
Fengcai Zhang ◽  
Yu Zhang ◽  
Qingfa Tan ◽  
Lili Lin ◽  
Xiaohua Liu ◽  
...  
2018 ◽  
Vol 5 (8) ◽  
pp. 1293-1296 ◽  
Author(s):  
Yong Xia ◽  
Fenzhen Chang ◽  
Lili Lin ◽  
Yali Xu ◽  
Xiaohua Liu ◽  
...  

An efficient asymmetric ring-opening reaction of cyclopropyl ketones with 2-naphthols has been realized using a chiral N,N′-dioxide–ScIII complex catalyst. A variety of chiral β-naphthol derivatives were obtained in excellent outcomes (up to 99% yield, 97% ee).


Synthesis ◽  
2020 ◽  
Vol 52 (12) ◽  
pp. 1738-1750 ◽  
Author(s):  
Zhuo Chai

The catalytic asymmetric ring-opening transformations of aziridines represent an important strategy for the construction of various chiral nitrogen-containing molecular architectures. This short review covers the progress achieved in the catalytic asymmetric transformation of racemic aziridines, focusing on the catalytic strategies employed for each different type of such aziridines.1 Introduction2 Reaction of Racemic 2-Vinylaziridines3 Reaction of Racemic 2-Alkylaziridines3.1 Regiodivergent Parallel Kinetic Resolution3.2 Kinetic Resolution4 Reaction of Racemic 2-(Hetero)arylaziridines4.1 Kinetic Resolution4.2 Enantioconvergent Transformation5 Reaction of Racemic Donor–Acceptor-Type Aziridines6 Conclusion and Outlook


ChemInform ◽  
2015 ◽  
Vol 46 (43) ◽  
pp. no-no
Author(s):  
Sifeng Li ◽  
Jianbin Xu ◽  
Baomin Fan ◽  
Zhiwu Lu ◽  
Chaoyuan Zeng ◽  
...  

2015 ◽  
Vol 21 (25) ◽  
pp. 9003-9007 ◽  
Author(s):  
Sifeng Li ◽  
Jianbin Xu ◽  
Baomin Fan ◽  
Zhiwu Lu ◽  
Chaoyuan Zeng ◽  
...  

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