Synthetic Studies on Optically Active b-Lactams. Asymmetric Synthesis of b-Lactams by the Cyclocondensation Utilizing Chiral Heterocyclic Compounds Derived from L-(+)-Tartaric Acid and (S)-Glutamic Acid

Heterocycles ◽  
1984 ◽  
Vol 22 (10) ◽  
pp. 2227 ◽  
Author(s):  
Nobuo Ikota ◽  
Akira HAnaki
2008 ◽  
Vol 80 (4) ◽  
pp. 763-776 ◽  
Author(s):  
Mikiko Sodeoka ◽  
Yoshitaka Hamashima

Highly enantioselective Pd(II)-catalyzed Michael addition, Mannich-type reaction, aldol reaction, fluorination, conjugate addition of amine, and conjugate reduction have been developed. Asymmetric synthesis of biologically interesting heterocyclic compounds, calycotomine, BMS-204352, torcetrapib, and warfarin, was achieved by using these Pd-catalyzed asymmetric reactions as a key step.


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