Recent advances in the stereoselective syntheses of acyclic disubstituted β2,3-amino acids

Abstract A wide variety of synthetic protocols have been developed during the past twenty years to the access of β2,3-amino acids as biologically interesting scaffolds in medicinal chemistry. The current account is devoted to provide an insight of the most relevant synthetic routes to this class of...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Kiss Loránd
Cherepanova Maria
Fülöp Ferenc
Dokumentumtípus: Cikk
Megjelent: 2015
Sorozat:TETRAHEDRON 71 No. 14
doi:10.1016/j.tet.2015.01.060

mtmt:2840227
Online Access:http://publicatio.bibl.u-szeged.hu/9905
Leíró adatok
Tartalmi kivonat:Abstract A wide variety of synthetic protocols have been developed during the past twenty years to the access of β2,3-amino acids as biologically interesting scaffolds in medicinal chemistry. The current account is devoted to provide an insight of the most relevant synthetic routes to this class of derivatives in racemic or enatiomerically pure form. The highlight focuses on the presentation of the stereoselective and stereocontrolled methodologies in view of efficiency and versatility, as well as limitations concerning stereocontrol, selectivity or large-scale synthesis. Relevant biological properties of these types of substances are also presented.
Terjedelem/Fizikai jellemzők:2049-2069
ISSN:0040-4020