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Porous graphitic carbon for the chromatographic separation of O-tetraacetyl-β-d-glucopyranosyl isothiocyanate-derivatised amino acid enantiomers

✍ Scribed by Weng C. Chan; Ruth Micklewright; David A. Barrett


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
253 KB
Volume
697
Category
Article
ISSN
1873-3778

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✍ Noriyuki Nimura; Haruo Ogura; Toshio Kinoshita 📂 Article 📅 1980 🏛 Elsevier Science 🌐 English ⚖ 359 KB

A novel method for reversed-phase high-performance liquid chromatographic resolution of amino acid enantiomers by the formation of diastereomers using 8 new chiral reagent, 2,3,4,6-tetra-O-acetyl+D-glucopyranosyl isothiocyanate (GITC), is described. GITC reacts readily with enantiomeric amino acids