Enantioselective Photocycloaddition Mediated by Chiral Brønsted Acids:  Asymmetric Synthesis of the Rocaglamides

2006 ◽  
Vol 128 (24) ◽  
pp. 7754-7755 ◽  
Author(s):  
Baudouin Gerard ◽  
Sheharbano Sangji ◽  
Daniel J. O'Leary ◽  
John A. Porco
2017 ◽  
Vol 15 (31) ◽  
pp. 6474-6477 ◽  
Author(s):  
Jianjun Li ◽  
Yiwei Fu ◽  
Cong Qin ◽  
Yang Yu ◽  
Hao Li ◽  
...  

A mild and efficient asymmetric cyclization reaction catalyzed by chiral Brønsted acids has been developed for the synthesis of chiral isoquinolinonaphthyridines.


2021 ◽  
Author(s):  
Liam McLean ◽  
Matthew Ashford ◽  
James Fyfe ◽  
Alexandra Slawin ◽  
Andrew Leach ◽  
...  

We report a method for the synthesis of chiral vicinal chlo-roamines via asymmetric protonation of catalytically gener-ated prochiral chloroenamines using chiral Brønsted acids. The process is highly enantioselective, with the origin of asymmetry and catalyst substituent effects elucidated by DFT calculations. We show the utility of the method as an approach to the synthesis of a broad range of heterocycle-substituted aziridines by treatment of the chloroamines with base in a one-pot process, as well as the utility of the process to allow access to vicinal diamines.


Tetrahedron ◽  
2012 ◽  
Vol 68 (12) ◽  
pp. 2728-2735 ◽  
Author(s):  
Huan Guan ◽  
Haining Wang ◽  
Deshun Huang ◽  
Yian Shi

2009 ◽  
Vol 11 (14) ◽  
pp. 3036-3039 ◽  
Author(s):  
Xiaofei Zeng ◽  
Xin Zeng ◽  
Zhenjiang Xu ◽  
Min Lu ◽  
Guofu Zhong

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