<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Graça, José</style></author><author><style face="normal" font="default" size="100%">Pereira, Helena</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Feruloyl Esters of ω-Hydroxyacids in Cork Suberin</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Wood Chemistry and Technology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cork</style></keyword><keyword><style  face="normal" font="default" size="100%">ferulic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Feruloyl esters</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS (voyant)</style></keyword><keyword><style  face="normal" font="default" size="100%">suberin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1998</style></year></dates><publisher><style face="normal" font="default" size="100%">Taylor &amp; Francis</style></publisher><volume><style face="normal" font="default" size="100%">18</style></volume><pages><style face="normal" font="default" size="100%">207-217</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Feruloyl esters of ?-hydroxyacids were found in the alcoholysis products of suberin from Quercus suber cork. Their identification was made from mass spectra and by comparison with synthetic model compounds. The co-hydroxyls of suberinic hydroxyacids are thought to be the ester-bonding points between suberin aliphatics and associated aromatics.</style></abstract><notes><style face="normal" font="default" size="100%">doi: 10.1080/02773819809349577</style></notes><research-notes><style face="normal" font="default" size="100%">doi: 10.1080/02773819809349577</style></research-notes></record></records></xml>