Dicobaltoctacarbonyl-mediated deoximation

Citation
C. Mukai et al., Dicobaltoctacarbonyl-mediated deoximation, SYNTHESIS-S, (11), 1999, pp. 1872-1874
Citations number
22
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
SYNTHESIS-STUTTGART
ISSN journal
00397881 → ACNP
Issue
11
Year of publication
1999
Pages
1872 - 1874
Database
ISI
SICI code
0039-7881(199911):11<1872:DD>2.0.ZU;2-6
Abstract
Treatment of oxime O-acetates with Co-2(CO)(8) in the presence of a base, f ollowed by H2O at room temperature efficiently afforded the parent carbonyl compounds in high yields. Direct regeneration of carbonyl functionalities from the corresponding oxime derivatives was realized by successive exposur e to acetylation conditions, Co-2(CO)(8) in the presence of base, and H2O. In addition, N-monosubstituted hydrazone derivatives could generate the par ent carbonyl compound under the above conditions.