A highly efficient michael addition of indoles to α,β-unsaturated electron-deficient compounds in acidic SDS micellar media

The Michael addition of indoles to α,β -unsaturated electron deficient compounds was catalyzed efficiently at room temperature in acidic micellar solution of sodium dodecyl sulfate (SDS). The substitution on the indole nucleus occurred exclusively at the 3-position in good to excellent yields, and n...

Full description

Saved in:
Bibliographic Details
Published in:Journal of the Iranian Chemical Society 2009-09, Vol.6 (3), p.588-593
Main Authors: Jafari, A. A., Moradgholi, F., Tamaddon, F.
Format: Article
Language:English
Subjects:
Analytical Chemistry
Biochemistry
Chemistry
Chemistry and Materials Science
Inorganic Chemistry
Organic Chemistry
Physical Chemistry
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The Michael addition of indoles to α,β -unsaturated electron deficient compounds was catalyzed efficiently at room temperature in acidic micellar solution of sodium dodecyl sulfate (SDS). The substitution on the indole nucleus occurred exclusively at the 3-position in good to excellent yields, and no N-alkylation products were observed.
ISSN:1735-207X
1735-2428
DOI:10.1007/BF03246538