Synthesis of δ-(l-α-aminoadipoyl)-l-cysteinyl-d-(O-methyl)-d-allothreonine a substrate for isopenicillin-N synthase and its O-methyl-d-threonine epimer
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Synthesis of δ-(α-aminoadipyl)cysteinylvaline and its role in penicillin biosynthesis
2. Penicillin biosynthesis: direct biosynthetic formation of penicillin V and penicillin G
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4. The biosynthesis of penicillins and cephalosporins
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1. Stereoselective Synthesis of Natural and Non-natural Thomsen-nouveau Antigens and Hydrazide Derivatives;Organic Letters;2015-05-19
2. The crystal structure of an isopenicillin N synthase complex with an ethereal substrate analogue reveals water in the oxygen binding site;FEBS Letters;2013-07-13
3. ChemInform Abstract: Synthesis of δ-(L-α-Aminoadipoyl)-L-cysteinyl-D- (O-methyl)-D-allothreonine a Substrate for Isopenicillin-N Synthase and Its O-Methyl-D-threonine Epimer.;ChemInform;2010-06-20
4. Serine and Threonine Schiff Base Esters React with β-Anomeric Peracetates in the Presence of BF3·Et2O to Produce β-Glycosides;Journal of Carbohydrate Chemistry;2010-05
5. Active-site-mediated elimination of hydrogen fluoride from a fluorinated substrate analogue by isopenicillin N synthase;Biochemical Journal;2004-08-24
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