<?xml version="1.0" encoding="utf-8"?>
<export-example>
  <doc>
    <id>2158</id>
    <completedYear/>
    <publishedYear>1998</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>104</pageFirst>
    <pageLast>110</pageLast>
    <pageNumber/>
    <edition/>
    <issue>1</issue>
    <volume>46</volume>
    <type>article</type>
    <publisherName>American Chemical Society</publisherName>
    <publisherPlace>Columbus, Ohio</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">New Melanoidin-like Maillard Polymers from 2-Deoxypentoses</title>
    <parentTitle language="eng">Journal of agricultural and food chemistry</parentTitle>
    <identifier type="old">2091</identifier>
    <identifier type="issn">0021-8561</identifier>
    <identifier type="issn">1520-5118</identifier>
    <enrichment key="bibliotheksstandort">Sonderstandort: Publica-Schrank</enrichment>
    <enrichment key="date_peer_review">15.01.2003</enrichment>
    <author>R. Tressl</author>
    <author>G. T. Wondrak</author>
    <author>Ralph-Peter Krüger</author>
    <author>D. Rewicki</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Maillard system 2-deoxy-D-ribose / methylamine</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Oligomerization of N-methyl-2-hydroxymethyl(and hydroxyl[13C]methyl)pyrrole</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Antioxidative activity</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Model compounds for melanoidins</value>
    </subject>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Physisches Exemplar in der Bibliothek der BAM vorhanden ("Hardcopy Access")</collection>
  </doc>
  <doc>
    <id>2159</id>
    <completedYear/>
    <publishedYear>1998</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>1765</pageFirst>
    <pageLast>1776</pageLast>
    <pageNumber/>
    <edition/>
    <issue>5</issue>
    <volume>46</volume>
    <type>article</type>
    <publisherName>American Chemical Society</publisherName>
    <publisherPlace>Columbus, Ohio</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Pentoses and Hexoses as Sources of New Melanoidin-like Maillard-Polymers</title>
    <parentTitle language="eng">Journal of agricultural and food chemistry</parentTitle>
    <identifier type="old">2092</identifier>
    <identifier type="issn">0021-8561</identifier>
    <identifier type="issn">1520-5118</identifier>
    <enrichment key="bibliotheksstandort">Sonderstandort: Publica-Schrank</enrichment>
    <enrichment key="date_peer_review">15.01.2003</enrichment>
    <author>R. Tressl</author>
    <author>G. T. Wondrak</author>
    <author>L.-A. Garbe</author>
    <author>Ralph-Peter Krüger</author>
    <author>D. Rewicki</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Model compounds for melanoidins</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Pyrroles from pentoses and hexoses</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Beta-dicarbonyl pathway of the Maillard reaction</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Polycondensation</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>MALDI-TOF-MS analysis</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Antioxidative activity of oligomeric model compounds</value>
    </subject>
    <collection role="literaturgattung" number="">Verlagsliteratur</collection>
    <collection role="fulltextaccess" number="">Physisches Exemplar in der Bibliothek der BAM vorhanden ("Hardcopy Access")</collection>
  </doc>
</export-example>
