41730-79-4Relevant articles and documents
Synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols or 3-amino alcohols using iodobenzene dichloride and sodium azide
He, Tian,Gao, Wen-Chao,Wang, Wei-Kun,Zhang, Chi
, p. 1113 - 1118 (2014/04/03)
A general and efficient method for the synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols and 3-amino alcohols has been developed using the same reagent combination of iodobenzene dichloride (PhICl2) and sodium azide (NaN3).
Mezlocillin: A Penicillin from the Acylureido Series / Synthesis and chemical properties
Koenig, H.-B.,Metzger, K. G.,Offe, H.-A.,Schroeck, W.
, p. 88 - 90 (2007/10/02)
Mezlocillin, 6--penicillanic acid, is a new semisynthetic acylureido-penicillin with a broad spectrum of antibacterial activity.The synthesis of mezlocillin from ampicillin and the from 6-aminopenicillanic acid and the physico-chemical properties are described.Mezlocillin is cleaved by penicillinase to the penicilloate which is degraded further by acids to the penilloate. - Key words: Acylureido series; Mezlocillin, chemical properties, synthesis; Penicillins
Penicillins
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, (2008/06/13)
Arylmethyl- and cyclohexenylmethyl- penicillins, substituted on the α-carbon atom of the side chain by a 2,3-disubstituted imidazolidinylcarbamido or a 2,3-disubstituted imidazolidinylthiocarbamido group, or by the corresponding 2,3-disubstituted 1,3-diazacyclohexylcarbamido or thiocarbamido groups are anti-bacterial agents.