Synthesis of 2-isoxazoline and α-hydroxy ketomethylene dipeptide isosteres

Authors
금교창정용준유은정김병현
Issue Date
1996-02
Publisher
Pergamon Press Ltd.
Citation
Bioorganic and Medicinal Chemistry, v.4, no.2, pp.209 - 225
Abstract
We have developed a simple and stereoselective method for synthesizing novel dipeptide isosteres using nitrile oxide cycloaddition as a key reaction. Employing this method, we have prepared efficiently various peptidomimetics containing 2-isoxazolines and α-hydroxy ketomethylene dipeptide isosteres.
Keywords
NITRILE OXIDE CYCLOADDITIONS; OPPOLZERS CHIRAL SULTAM; AMINO ALDEHYDES; ASYMMETRIC INDUCTION; ORGANIC-SYNTHESIS; PRACTICAL METHOD; AIDS; PEPTIDE; RENIN; DELTA-2-ISOXAZOLINES; dipeptitde isostere; peptidomimetics; nitrile oxide cyclo-addition; 2-isoxazoline; α-hydroxy ketomethylene
ISSN
0968-0896
URI
https://pubs.kist.re.kr/handle/201004/144538
DOI
10.1016/0968-0896(95)00174-3
Appears in Collections:
KIST Article > Others
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE