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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://repozitorij.uni-lj.si/IzpisGradiva.php?id=132354"><dc:title>Application of the N-dibenzyl protective group in the preparation of β-lactam pseudopeptides</dc:title><dc:creator>Frlan,	Rok	(Avtor)
	</dc:creator><dc:creator>Hrast Rambaher,	Martina	(Avtor)
	</dc:creator><dc:creator>Gobec,	Stanislav	(Avtor)
	</dc:creator><dc:subject>β-lactams</dc:subject><dc:subject>dibenzylamino</dc:subject><dc:subject>Mitsunobu reaction</dc:subject><dc:subject>nocardicin</dc:subject><dc:subject>pseudopeptides</dc:subject><dc:description>Despite the great importance of β-lactam antibiotics, there is still a limited number of synthetic approaches for the formation of β-lactam containing dipeptides. In this study, we report upon the stereoselective preparation of β-lactam-containing pseudopeptides, where different reaction conditions and NH$_2$ protective groups were tested to obtain compounds that contain 3-amino-azetidin-2-one. We demonstrate that the protective group is essential for the outcome of the reaction. Successful implementation of dibenzyl-protected serine-containing dipeptides through the Mitsunobu reaction can provide the desired products at high yields and stereoselectivity.</dc:description><dc:date>2019</dc:date><dc:date>2021-10-22 11:43:38</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>132354</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
