Phenolic extractives have been isolated from Douglas-fir sapwood and h
eartwood and identified by NMR and mass spectroscopy. Pinocembrin, [5,
5']-bisdihydroquercetin and two lignans, pinoresinol and roxymethyl-5-
(3-hydroxypropyl)-7-methoxybenzofuran are reported for the first time
in these tissues. The chemical structures of these phenolic extractive
s show that heartwood formation is characterized by both primary (bios
ynthetic) and secondary reactions. Secondary reactions include hydroly
sis of phenol glucosides and oxidative polymerization. (C) 1997 Elsevi
er Science Ltd. All rights reserved.