Chemical studies of the Proteaceae. V. Synthesis of derivatives of 5-n-Alkylresorcinols and related compounds

Publisher Website
Google Scholar
Abstract
A convenient reaction sequence in which the key step is a Stevens rearrangement, leading to dimethyl ethers of 5-n-alkylresorcinols has been developed and exemplified by the synthesis of the dimethyl ethers of the natural phenols, dihydropersoonol, grevillol, and bilobol. The tetramethyl ether of bis-norstriatol was also synthesized by the same route.

This publication has 0 references indexed in Scilit: