ALTERING THE REACTION PATHWAYS OF AMINOPYRIDINE WITH 4,5-DIAZAFLUORENONE - METAL-ION CONTROL

Authors
WANG YX RILLEMA DP
Citation
Yx. Wang et Dp. Rillema, ALTERING THE REACTION PATHWAYS OF AMINOPYRIDINE WITH 4,5-DIAZAFLUORENONE - METAL-ION CONTROL, Tetrahedron letters, 38(38), 1997, pp. 6627-6630
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
38
Issue
38
Year of publication
1997
Pages
6627 - 6630
Database
ISI
SICI code
0040-4039(1997)38:38<6627:ATRPOA>2.0.ZU;2-7
Abstract
A parallel study of the ligand 4,5-diazafluorenone reactivity in the p resence and absence of ruthenium(II) ion revealed that the reaction pa thway of the ligand 4,5-diazafluoren-9-one with aminopyridine can be a ltered from the normal Schiff-base reaction to an unusual ring opening reaction upon its coordination to ruthenium(II) ion. (C) 1997 Elsevie r Science Ltd.