STEREOSELECTIVE CYCLOADDITION REACTIONS OF CARBOHYDRATE-DERIVATIVES

Citation
P. Herczegh et al., STEREOSELECTIVE CYCLOADDITION REACTIONS OF CARBOHYDRATE-DERIVATIVES, Pure and applied chemistry, 69(3), 1997, pp. 519-524
Citations number
16
Categorie Soggetti
Chemistry
Journal title
ISSN journal
00334545
Volume
69
Issue
3
Year of publication
1997
Pages
519 - 524
Database
ISI
SICI code
0033-4545(1997)69:3<519:SCROC>2.0.ZU;2-D
Abstract
Structural analogs of swainsonine and castanospermine have been synthe sized using [4+2] cycloadditions of chiral azomethines with Danishefsk y diene. Similar hydroxyindolizidines were prepared by [3+2] dipolar c ycloadditions of sugar derived cyclic nitrones with methyl acrylate. S tereoselectivity of [2+2] photocycloadditions of uridine derivatives w as also studied.