ChemInform Abstract: SYNTHETIC STUDIES ON OPTICALLY ACTIVE β-LACTAMS. ASYMMETRIC SYNTHESIS OF β-LACTAMS BY THE CYCLOCONDENSATION UTILIZING CHIRAL HETEROCYCLIC COMPOUNDS DERIVED FROM L-(+)-TARTARIC ACID AND (S)-GLUTAMIC ACID

1985 ◽  
Vol 16 (18) ◽  
Author(s):  
N. IKOTA ◽  
A. 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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