An efficient sulfenylation of aromatics using highly active quinone mono O,S-acetal bearing a pentafluorophenylthio group

Authors
Matsugi, M Murata, K Nambu, H Kita, Y
Citation
M. Matsugi et al., An efficient sulfenylation of aromatics using highly active quinone mono O,S-acetal bearing a pentafluorophenylthio group, TETRAHEDR L, 42(6), 2001, pp. 1077-1080
Citations number
14
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
42
Issue
6
Year of publication
2001
Pages
1077 - 1080
Database
ISI
SICI code
0040-4039(20010205)42:6<1077:AESOAU>2.0.ZU;2-P
Abstract
A facile sulfenylation of various aromatic nuclei was achieved by use of th e novel sulfenylation reagent, the quinone mono O,S-acetal bearing a pentaf luorophenylthio group. This reagent functions below 0 degreesC in the prese nce of a catalytic amount of TMSOTf. (C) 2001 Elsevier Science Ltd. All rig hts reserved.