A conventional route for the synthesis of new oxazolidin-2-one derivatives with beta-aminoalanines.
Fumiko Fujisaki, Nobuhiro Abe, Kunihiro Sumoto
Index: Chem. Pharm. Bull. 52(10) , 1238-41, (2004)
Full Text: HTML
Abstract
A conventional new route to the novel oxazolidin-2-one derivatives (3a-f) having two substituents on N-3 and C-4 in the oxazolidin-2-one ring was established with racemic beta-aminoalanine derivatives (1) as the key starting materials.
Related Compounds
Related Articles:
2013-06-27
[J. Med. Chem. 56(12) , 5079-93, (2013)]
2012-01-01
[J. Inorg. Biochem. 106(1) , 111-6, (2012)]
Synthesis of 9-membered dilactams derived from 1,3-diaminopropionic and glutamic acids.
2004-03-01
[J. Pept. Res. 63(3) , 235-40, (2004)]
New 2,3-diaminopropionic acid inhibitors of AGE and ALE formation.
2013-02-07
[Org. Biomol. Chem. 11(5) , 773-80, (2013)]
2010-06-14
[ChemBioChem. 11(9) , 1266-72, (2010)]