| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278234 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
The cyclization of the dianions of diethyl 2-oxopropylphosphonate and of acetone with 1,1-diacylopropanes afforded hydroxyspiro[5.2]cyclooctenones which were transformed, by homo-Michael reactions with tetrabutylammonium halides, into various functionalized phenols or their dimers.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Synthesis and reactions of hydroxyspiro[5.2]cyclooctenones based on the cyclization of the dianions of acetone and diethyl 2-oxopropylphosphonate with 1,1-diacylcyclopropanes](/preview/png/5278234.png "First Page Preview: Synthesis and reactions of hydroxyspiro[5.2]cyclooctenones based on the cyclization of the dianions of acetone and diethyl 2-oxopropylphosphonate with 1,1-diacylcyclopropanes")
Authors
Nasir Rasool, Muhammad A. Rashid, Muhammad Adeel, Helmar Görls, Peter Langer,