<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Acetylated glucose fatty ester &#8211; Journal of Oil Palm Research</title>
	<atom:link href="https://jopr.mpob.gov.my/tag/acetylated-glucose-fatty-ester/feed/" rel="self" type="application/rss+xml" />
	<link>https://jopr.mpob.gov.my</link>
	<description></description>
	<lastBuildDate>Wed, 17 Nov 2021 02:44:59 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.0</generator>
	<item>
		<title>SYNTHESIS AND CHARACTERIZATION OF ACETYLATED GLUCOSE FATTY ESTERS FROM PALM AND PALM KERNEL OIL FATTY METHYL ESTERS</title>
		<link>https://jopr.mpob.gov.my/synthesis-and-characterization-of-acetylated-glucose-fatty-esters-from-palm-and-palm-kernel-oil-fatty-methyl-esters/</link>
		
		<dc:creator><![CDATA[mpob_admin]]></dc:creator>
		<pubDate>Sat, 13 Nov 2021 15:42:08 +0000</pubDate>
				<category><![CDATA[Vol. 12 No. 2 December 2000]]></category>
		<category><![CDATA[interesterification]]></category>
		<category><![CDATA[Acetylated glucose fatty ester]]></category>
		<category><![CDATA[antimicrobial activity]]></category>
		<category><![CDATA[cytotoxicity]]></category>
		<category><![CDATA[HLB]]></category>
		<category><![CDATA[phase diagram]]></category>
		<guid isPermaLink="false">https://jopr.mpob.gov.my/V2/?p=9363</guid>

					<description><![CDATA[Acetylated glucose fatty esters (AGFE) were synthesized from palm and palm kernel fatty acid methyl esters (FAME) through a one-stage solvent-free interesterfication reaction with glucose pentaacetate (GPA). Two main products obtained and identified were mono-and di-substituted AGFEE. The hydrophile-lipophile balance (HLB), ternary phase diagram, cytotoxicity and antimicrobial bioassays were studied.]]></description>
										<content:encoded><![CDATA[<p style="text-align: justify;">Acetylated glucose fatty esters (AGFE) were synthesized from palm and palm kernel fatty acid methyl esters (FAME) through a one-stage solvent-free interesterfication reaction with glucose pentaacetate (GPA). Two main products obtained and identified were mono-and di-substituted AGFEE. The hydrophile-lipophile balance (HLB), ternary phase diagram, cytotoxicity and antimicrobial bioassays were studied.</p>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>FATTY ACYL SUBSTITUENT-INDUCED CHANGES IN C-CHEMICAL SHIFTS OF CARBONYL CARBONS: A TOOL FOR STRUCTURAL ELUCIDATION IN ACETYLATED GLUCOSE ESTERS OF PALM FATTY ACID</title>
		<link>https://jopr.mpob.gov.my/fatty-acyl-substituent-induced-changes-in-c-chemical-shifts-of-carbonyl-carbons-a-tool-for-structural-elucidation-in-acetylated-glucose-esters-of-palm-fatty-acid/</link>
		
		<dc:creator><![CDATA[mpob_admin]]></dc:creator>
		<pubDate>Sat, 13 Nov 2021 15:42:35 +0000</pubDate>
				<category><![CDATA[Vol. 12 No. 1 June 2000]]></category>
		<category><![CDATA[Acetylated glucose fatty ester]]></category>
		<category><![CDATA[polyacetylated glucopyranose]]></category>
		<category><![CDATA[substituent-induced-chemical shift]]></category>
		<category><![CDATA[interesterification]]></category>
		<guid isPermaLink="false">https://jopr.mpob.gov.my/V2/?p=9368</guid>

					<description><![CDATA[Substituent-induced changes (SIC) in 13C-chemical shifts of carbonyl carbon atoms upon interesterification of glucose pentaacetate (GPA) with fatty acid methyl esters (FAME) of stripped palm kernel oil (SPKO), palm oil (PO) and capric (C10) acid, were used to determine the number and positions of the fatty acid substituents on the pyranosyl ring. Results show that [&#8230;]]]></description>
										<content:encoded><![CDATA[<p style="text-align: justify;">Substituent-induced changes (SIC) in 13C-chemical shifts of carbonyl carbon atoms upon interesterification of glucose pentaacetate (GPA) with fatty acid methyl esters (FAME) of stripped palm kernel oil (SPKO), palm oil (PO) and capric (C<sub>10</sub>) acid, were used to determine the number and positions of the fatty acid substituents on the pyranosyl ring. Results show that SIC on the ring carbon and ring proton atoms are not always consistent with the molecular structures. But SIC on the carbonyl carbon atoms are however unambiquous and consistent with molecular structures of all the products. The analysis of <sup>13</sup>C-chemical shift changes of carbonyl carbon therefore provides a means to determine the number and positions of fatty acyl groups in polyacetylated glucopyranoses</p>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>SELECTIVITY AND KINETICS OF INTERESTERIFICATION REACTION OF GLUCOSE PENTAACETATE WITH FATTY ACID METHYL ESTERS</title>
		<link>https://jopr.mpob.gov.my/selectivity-and-kinetics-of-interesterification-reaction-of-glucose-pentaacetate-with-fatty-acid-methyl-esters/</link>
		
		<dc:creator><![CDATA[mpob_admin]]></dc:creator>
		<pubDate>Sat, 13 Nov 2021 08:13:49 +0000</pubDate>
				<category><![CDATA[Vol. 13 No. 1 June 2001]]></category>
		<category><![CDATA[kinetic]]></category>
		<category><![CDATA[interesterification reaction]]></category>
		<category><![CDATA[palm oil]]></category>
		<category><![CDATA[Acetylated glucose fatty ester]]></category>
		<guid isPermaLink="false">https://jopr.mpob.gov.my/V2/?p=9101</guid>

					<description><![CDATA[Acetylated glucose fatty esters (AGFEs) were prepared by a solvent-free interesterification reaction of glucose pentaacetate (GPA) and mixed fatty acid methyl ester (FAME) of palm oil (PO)-based fatty acids. The relative selectivity of fatty acyl groups towards the GPA ring and the kinetics of the interesterification process were studied. The selectivity studies have shown that [&#8230;]]]></description>
										<content:encoded><![CDATA[<p style="text-align: justify;">Acetylated glucose fatty esters (AGFEs) were prepared by a solvent-free interesterification reaction of glucose pentaacetate (GPA) and mixed fatty acid methyl ester (FAME) of palm oil (PO)-based fatty acids. The relative selectivity of fatty acyl groups towards the GPA ring and the kinetics of the interesterification process were studied. The selectivity studies have shown that the longer chain fatty acyl groups were preferred in the interesterification process involving GPA and FAMEs. In the C<sub>6</sub> to C<sub>l0</sub> fatty acids group C<sub> l0</sub> was the most favoured, while C<sub>18:1</sub> had the highest selectivity in the C<sub>12</sub> to C<sub>18:2</sub>group. The results also showed that the reactions involving oleic-FAME and C<sub>6-10</sub>-FAME proceeded via zero-order kinetics with respect to GPA</p>
]]></content:encoded>
					
		
		
			</item>
	</channel>
</rss>
