Phytochemical studies. Part V. The synthesis of Taiwanin A
Journal of the Chemical Society C: Organic Pub Date : , DOI:10.1039/J39670000161
Abstract
Conversion of dipiperonylidenesuccinic anhydride into the ethyl hydrogen ester, followed by reduction with lithium borohydride, gave a hydroxy-acid, which on treatment with toluene-p-sulphonic acid, produced taiwanin A.