1,3-DIPOLAR CYCLOADDITION APPROACH TOWARDS THE STEREOSELECTIVE PREPARATION OF AZA-CEPHALOTAXINE SKELETON

Authors
NYERGES M BITTER I KADAS I TOTH G TOKE L
Citation
M. Nyerges et al., 1,3-DIPOLAR CYCLOADDITION APPROACH TOWARDS THE STEREOSELECTIVE PREPARATION OF AZA-CEPHALOTAXINE SKELETON, Tetrahedron, 51(42), 1995, pp. 11489-11502
Citations number
37
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
51
Issue
42
Year of publication
1995
Pages
11489 - 11502
Database
ISI
SICI code
0040-4020(1995)51:42<11489:1CATTS>2.0.ZU;2-Q
Abstract
An aza-analogue of cephalotaxine I has been prepared stereoselectivly using 1,3-dipolar cycloaddition of azomethine ylide as a key step.