Catalytic asymmetric ring opening of epoxides to chlorohydrins with mild chloride donors and enantiopure titanium complexes

1999 ◽  
Vol 10 (8) ◽  
pp. 1563-1569 ◽  
Author(s):  
Stefan Bruns ◽  
Günter Haufe
2014 ◽  
Vol 25 (10-11) ◽  
pp. 838-843 ◽  
Author(s):  
Victor I. Maleev ◽  
Denis A. Chusov ◽  
Lidiya V. Yashkina ◽  
Nikolai S. Ikonnikov ◽  
Michail M. Il’in

ChemInform ◽  
2014 ◽  
Vol 45 (50) ◽  
pp. no-no
Author(s):  
Victor I. Maleev ◽  
Denis A. Chusov ◽  
Lidiya V. Yashkina ◽  
Nikolai S. Ikonnikov ◽  
Michail M. Il'in

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


2000 ◽  
Vol 122 (8) ◽  
pp. 1828-1829 ◽  
Author(s):  
Gabriel S. Weatherhead ◽  
J. Gair Ford ◽  
Erik J. Alexanian ◽  
Richard R. Schrock ◽  
Amir H. Hoveyda

Sign in / Sign up

Export Citation Format

Share Document