Mild and convenient oxidation of aromatic heterocyclic primary alcohols by4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium perchlorate

Authors
Kernag, CA Bobbitt, JM McGrath, DV
Citation
Ca. Kernag et al., Mild and convenient oxidation of aromatic heterocyclic primary alcohols by4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium perchlorate, TETRAHEDR L, 40(9), 1999, pp. 1635-1636
Citations number
20
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
9
Year of publication
1999
Pages
1635 - 1636
Database
ISI
SICI code
0040-4039(19990226)40:9<1635:MACOOA>2.0.ZU;2-7
Abstract
Hydroxymethyl substituted aromatic heterocycles, including pyridines, furan s, and thiophenes, are oxidized to the corresponding aldehydes in excellent yields by 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium perchl orate (1) with minimal workup. (C) 1999 Elsevier Science Ltd. All rights re served.