USING A RIGID MOLECULE TRICYCLODECADIENONE FOR THE STEREOSPECIFIC SYNTHESIS OF THE CHAIN COMPOUND SENECIVERNIC ACID

Authors
LIU ZY ZHAO LY XIE YN WU Y WONG LL ZHENG H
Citation
Zy. Liu et al., USING A RIGID MOLECULE TRICYCLODECADIENONE FOR THE STEREOSPECIFIC SYNTHESIS OF THE CHAIN COMPOUND SENECIVERNIC ACID, Journal of the Chemical Society. Perkin transactions. I (Print), (14), 1998, pp. 2127-2129
Citations number
12
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I (Print) → ACNP
ISSN journal
0300922X
Issue
14
Year of publication
1998
Pages
2127 - 2129
Database
ISI
SICI code
0300-922X(1998):14<2127:UARMTF>2.0.ZU;2-Z
Abstract
The highly efficient synthesis of a chain compound, senecivernic acid 2, using a rigid molecule, tricyclodecadienone 1, as the starting mate rial via a retro-Diels-Alder reaction as the key step and without usin g any protecting groups is described in a total of ten steps and in 50 % overall yield.