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            <title>fmoc cys trt oh	-	Fmoc-L-Cys(Trt)-OH; (R)-2-Fmoc-3-tritylsulfanyl-propionic...</title>
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            <pubDate>Sun, 21 Feb 2021 16:25:37 GMT</pubDate>
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            <title>fmoc n ethyl hydroxylamine	-	9H-fluoren-9-ylmethyl N-ethyl-N-hydroxycarbamate</title>
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            <pubDate>Thu, 26 Nov 2020 13:15:10 GMT</pubDate>
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            <title>fmoc phe oh	-	L-Phenylalanine derivative is used in the preparation of...</title>
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            <description>&lt;p&gt;&lt;a href="https://www.23hq.com/bocsci2018/photo/77901186"&gt;&lt;img src="https://www.23hq.com/67659407/77901186_a16e8e6ebf364aa204f792f4ed9083a8_standard.jpg" width="460" height="258" class="23-standard"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a rel="nofollow" href="https://aapep.bocsci.com/product/fmoc-l-phenylalanine-cas-35661-40-6-294250.html"&gt;fmoc phe oh&lt;/a&gt;	-	L-Phenylalanine derivative is used in the preparation of peptides and deltorphin derivatives. A potential inhibitor of IGF-I and IGF-Binding Protein-5 complex.&lt;/p&gt;&lt;p&gt;Photo by &lt;a href="https://www.23hq.com/bocsci2018/"&gt;bocsci2018&lt;/a&gt;&lt;/p&gt;</description>
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            <pubDate>Thu, 26 Nov 2020 13:15:00 GMT</pubDate>
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            <title>fmoc asp odmab oh	-	The Dmab group can be cleaved selectively in the presence...</title>
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            <description>&lt;p&gt;&lt;a href="https://www.23hq.com/bocsci2018/photo/77901185"&gt;&lt;img src="https://www.23hq.com/67659475/77901185_fe777e8da0f78fe23b8b944f9ade26e9_standard.jpg" width="460" height="315" class="23-standard"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a rel="nofollow" href="https://aapep.bocsci.com/product/fmoc-l-aspartic-acid-4-n-1-4-4-dimethyl-cas-269066-08-2-89019.html"&gt;fmoc asp odmab oh&lt;/a&gt;	-	The Dmab group can be cleaved selectively in the presence of tBu-based protected groups by treatment with 2% hydrazine in DMF, making this derivative an extremely useful tool for the preparation of cyclic peptides by FMOC SPPS.&lt;/p&gt;&lt;p&gt;Photo by &lt;a href="https://www.23hq.com/bocsci2018/"&gt;bocsci2018&lt;/a&gt;&lt;/p&gt;</description>
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            <pubDate>Thu, 26 Nov 2020 13:14:56 GMT</pubDate>
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            <title>fmoc glycine	-	N-Fmoc-glycine is an N-Fmoc-protected form of Glycine. Glycine...</title>
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            <description>&lt;p&gt;&lt;a href="https://www.23hq.com/bocsci2018/photo/77901181"&gt;&lt;img src="https://www.23hq.com/67659407/77901181_85241a201e568099987a7b50895bffda_standard.jpg" width="460" height="315" class="23-standard"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a rel="nofollow" href="https://aapep.bocsci.com/product/fmoc-glycine-cas-29022-11-5-342530.html"&gt;fmoc glycine&lt;/a&gt;	-	N-Fmoc-glycine is an N-Fmoc-protected form of Glycine. Glycine is a non-essential amino acid that acts as an inhibitory neyrotransmitter in the vertebrate central nervous system. Glycine also posesses cytoprotective effect against oxidant damage in the kidney.&lt;/p&gt;&lt;p&gt;Photo by &lt;a href="https://www.23hq.com/bocsci2018/"&gt;bocsci2018&lt;/a&gt;&lt;/p&gt;</description>
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            <pubDate>Thu, 26 Nov 2020 13:14:52 GMT</pubDate>
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            <title>fmoc tyr me oh	-	Fmoc-L-Tyr(Me)-OH; Fmoc-p-methoxy-Phe-OH;...</title>
            <link>https://www.23hq.com/bocsci2018/photo/76296907</link>
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            <pubDate>Wed, 21 Oct 2020 14:37:18 GMT</pubDate>
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            <title>fmoc arg pbf oh	-	Fmoc-L-Arg(Pbf)-OH;...</title>
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            <description>&lt;p&gt;&lt;a href="https://www.23hq.com/bocsci2018/photo/76296901"&gt;&lt;img src="https://www.23hq.com/67659474/76296901_78f5abd2842086d32cabf62b555b5478_standard.jpg" width="460" height="345" class="23-standard"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a rel="nofollow" href="https://aapep.bocsci.com/product/n-fmoc-n-2-2-4-6-7-pentamethyldihydro-cas-154445-77-9-59689.html"&gt;fmoc arg pbf oh&lt;/a&gt;	-	Fmoc-L-Arg(Pbf)-OH; (S)-2-((((9H-Fluoren-9-Yl)Methoxy)Carbonyl)Amino)-5-(3-((2,2,4,6,7-Pentamethyl-2,3-Dihydrobenzofuran-5-Yl)Sulfonyl)Guanidino)Pentanoic Acid; Nalpha-Fmoc-Nomega-Pbf-L-Arginine&lt;/p&gt;&lt;p&gt;Photo by &lt;a href="https://www.23hq.com/bocsci2018/"&gt;bocsci2018&lt;/a&gt;&lt;/p&gt;</description>
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            <pubDate>Wed, 21 Oct 2020 14:37:13 GMT</pubDate>
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            <title>fmoc amino acids	The general Fmoc-protected amino acids synthesis step is to...</title>
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            <description>&lt;p&gt;&lt;a href="https://www.23hq.com/bocsci2018/photo/74704855"&gt;&lt;img src="https://www.23hq.com/67659474/74704855_2a23074bb5dcd4cebbddc7fa956e7535_standard.jpg" width="460" height="407" class="23-standard"/&gt;&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a rel="nofollow" href="https://aapep.bocsci.com/amino-acids/fmoc-amino-acids-3264.html"&gt;fmoc amino acids&lt;/a&gt;	The general Fmoc-protected amino acids synthesis step is to add the amino acids to a mixed solution of water and sodium bicarbonate with stirring and cool the resulting solution to 5 °C, then slowly add Fmoc-OSu or Fmoc-Cl. After the resulting mixture is kept at 0 °C for 1 hour, and then heat to room temperature for one night. Then water is added and the aqueous layer is extracted twice with EtOAc. The organic layer is back extracted with saturated sodium bicarbonate solution twice. The combined aqueous layer is acidified to pH 1 with 10% hydrochloric acid and then extracted with EtOAc for 3 times. The combined organic layers are dried (sodium sulfate) and concentrated in vacuo and the resulting residue could be purified by flash chromatography (SiO).&lt;/p&gt;&lt;p&gt;Photo by &lt;a href="https://www.23hq.com/bocsci2018/"&gt;bocsci2018&lt;/a&gt;&lt;/p&gt;</description>
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            <pubDate>Mon, 14 Sep 2020 11:49:13 GMT</pubDate>
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