An expedient synthesis of oxindole dimers by direct oxidative dimerization of oxindoles

Cited 11 time in scopus
Metadata Downloads
Title
An expedient synthesis of oxindole dimers by direct oxidative dimerization of oxindoles
Author(s)
H J Lee; Sangku Lee; J W Lim; J N Kim
Bibliographic Citation
Bulletin of Korean Chemical Society, vol. 34, no. 8, pp. 2446-2450
Publication Year
2013
Abstract
Oxindole dimers have been used as intermediates in the synthesis of various cyclotryptamine alkaloids. An efficient direct synthesis of oxindole dimers has been carried out from 3-substituted oxindoles via an oxidative dimerization using manganese(III) acetate or copper acetate/silver acetate system.
Keyword
Manganese(III) acetateOxidative dimerizationOxindole dimersOxindoles
ISSN
0253-2964
Publisher
Wiley
DOI
http://dx.doi.org/10.5012/bkcs.2013.34.8.2446
Type
Article
Appears in Collections:
Ochang Branch Institute > Anticancer Agent Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.